The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index; 35 of the 65 sources its claims cite were checked for support.
E‐cadherin is essential for in vivo epidermal barrier function by regulating tight junctions
Open accessAbstract
Cadherin adhesion molecules are key determinants of morphogenesis and tissue architecture. Nevertheless, the molecular mechanisms responsible for the morphogenetic contributions of cadherins remain poorly understood in vivo. Besides supporting cell-cell adhesion, cadherins can affect a wide range of cellular functions that include activation of cell signalling pathways, regulation of the cytoskeleton and control of cell polarity. To determine the role of E-cadherin in stratified epithelium of the epidermis, we have conditionally inactivated its gene in mice. Here we show that loss of E-cadherin in the epidermis in vivo results in perinatal death of mice due to the inability to retain a functional epidermal water barrier. Absence of E-cadherin leads to improper localization of key tight junctional proteins, resulting in permeable tight junctions and thus altered epidermal resistance. In addition, both Rac and activated atypical PKC, crucial for tight junction formation, are mislocalized. Surprisingly, our results indicate that E-cadherin is specifically required for tight junction, but not desmosome, formation and this appears to involve signalling rather than cell contact formation.
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Written from the paper’s full text.
TL;DR
Conditional loss of E-cadherin in mouse epidermis causes perinatal death from water loss due to impaired tight junction function, while desmosomes and cell-cell contacts remain largely intact. E-cadherin appears to regulate tight junction formation via signalling, involving mislocalization of activated aPKC and Rac rather than loss of adhesion per se.
Key findings
- K14-Cre/Ecad Fl/À mice died perinatally around 7–12 h after birth, lost about 9% body weight versus about 3% in controls, had increased haematocrit, and showed increased transepidermal water loss.
- The outside-in barrier remained functional, but inside-out permeability was impaired: biotin penetrated the granular layer to the stratum corneum, and epidermal resistance was three-fold lower in mutant skin than control skin, with dermal resistance not significantly affected (N=8 control, N=4 mutant; P=0.03).
- Tight junction components were mislocalized in mutant epidermis: claudin-1 was absent from the granular layer, claudin-4 showed punctate membrane distribution with less protein, and ZO-1 distribution was altered; occludin remained enriched at the membrane.
- Desmosomes formed normally and desmosomal cadherin expression was upregulated; P-cadherin was upregulated mainly in the basal layer. Activated aPKC was absent or largely diminished at suprabasal cell-cell borders, and Rac membrane localization was lost or diminished, while total activated Rac levels were unchanged.
Methods
- E-cadherin was conditionally inactivated in developing mouse epidermis using the Cre-loxP system with K14-Cre and floxed E-cadherin alleles, generating K14-Cre/Ecad Fl/Fl or K14-Cre/Ecad Fl/À mice; only data on K14-Cre/Ecad Fl/À mice are described because no phenotypic difference was found between lines.
- Analyses included RT-PCR, immunohistochemistry, Western blot, ultrastructural electron microscopy, weight and haematocrit measurements, TEWL measurement, lucifer yellow and toluidine blue penetration assays, intradermal biotin inside-out permeability assays, impedance analysis of skin biopsies, and Rac activation assays.
- Samples included newborn mice and embryonic stages E15.5, E16.5, and E18.5, depending on the assay.
Limitations
- The paper states that it remains unclear whether loss of E-cadherin impairs recruitment of activated aPKC to the membrane or whether aPKC is first recruited to adherens junctions and subsequently activated; it also notes that changes in activated Cdc42 may not be reflected by total Cdc42 levels.
- The paper states that the cornified layer may contribute to water loss in the mutants, although it is most likely not the primary cause.
- Evident from the text: many mechanistic conclusions are correlative and based on localization or protein-level changes rather than rescue experiments; impedance measurements used a small mutant sample (N=4); and only the K14-Cre/Ecad Fl/À line is described in the results.
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Claims the paper makes
70 Own result · 40 Own interpretation · 21 No full text of the sources · 13 Supported · 10 Partly supported · 7 No basis given · 1 Supported so far · 1 Mixed support · 1 Sources not found · 1 Not checked yet · 1 Own method · accuracy not yet measured
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“As described previously (Young et al, 2003;Tinkle et al, 2004), no difference in localization of desmosomal markers like plakoglobin, desmocollin 2 and desmoglein 1/2 was observed (Figure 3A).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Cell-cell contacts are maintained in the absence of E-cadherin
What the sources say
- Partly supportedcites Young et al, 2003 sourceExperimental — accuracy not yet measured
The ‘Ablation of E-cadherin alters epidermal differentiation’ section (page not provided) says desmoglein expression was comparable in mutant and control tissue, and the Figure 6 caption reports similar localization of desmoplakin. The copy also reports preserved desmosomes, but it does not establish unchanged localization for plakoglobin or desmocollin 2, or specify desmoglein 1/2. (LLM, conf=0.86)
- Partly supportedcites Tinkle et al, 2004 sourceExperimental — accuracy not yet measured
The Results (Fig. 2 F and G; page not available) report largely similar plakoglobin levels in wild-type and E-cadherin knockout epidermis, but do not explicitly establish unchanged localization. The Results also report increased desmosomal cadherins by immunofluorescence in knockout spinous layers (Fig. 2 E), rather than an unchanged signal for desmogleins 1/2. Our copy does not report a comparison for desmocollin 2. (LLM, conf=0.82)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“In control skin, biotin moves up to the stratum granulosum, where it is halted due to the presence of tight junctions, marked by occludin staining, between the cells of the granular layer (Furuse et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
What the sources say
- Supportedcites Furuse et al, 2002 source
The Results section, under “Barrier functions of TJs in the epidermis” (Fig. 8), reports that in wild-type newborn mouse skin, the biotinylation reagent diffused to the second layer of the stratum granulosum and was stopped at occludin-positive tight junctions. The Discussion locates those junctions along the lateral membranes of granular cells. The claim accurately paraphrases this finding for control skin. (LLM, conf=0.94)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“These mice also have an apparently normal cornified envelope.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
What the sources say
- Supportedcites Furuse et al, 2002 source
In Results, “Stratum corneum in claudin-1–deficient mice” (Fig. 9B), the authors report that cornified cell envelopes isolated from claudin-1–deficient epidermis were morphologically indistinguishable from those of wild-type epidermis. This directly supports the claim that they had an apparently normal cornified envelope. (LLM, conf=0.95)
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Their importance in maintaining the epidermal barrier was underscored by the observations that in vivo inactivation of the tight junctional membrane protein claudin-1 results in epidermal water loss and ultimately in neonatal death of the mice (Furuse et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Supportedcites Furuse et al, 2002 source
The Results report that only claudin-1–deficient newborn mice showed excessive transepidermal water loss and that all homozygous mutants died within one day of birth. The Discussion reports both findings while noting that it could not conclusively establish whether dehydration caused death; the citing sentence attributes both outcomes to claudin-1 inactivation, not explicitly one to the other. (LLM, conf=0.92)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Like occludin, claudin-4 is found at the membrane in the granular layer of the epidermis in control mice (Furuse et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
What the sources say
- Supportedcites Furuse et al, 2002 source
The Results section (Fig. 4B; page not supplied) reports claudin-4 in the second and third layers of the stratum granulosum of wild-type mice, concentrated at occludin-positive lines around granular cells. This supports its membrane localization in the granular layer of control mice. (LLM, conf=0.93)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Rac was found at the membrane in control mice, consistent with its function in cell-cell contact formation (Ehrlich et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
What the sources say
- Partly supportedcites Ehrlich et al, 2002 sourceExperimental — accuracy not yet measured
The passage describing Figure 2A reports RacGFP accumulating along newly contacting membranes, supporting membrane localization during cell-cell contact formation. The Experimental Procedures describe cultured MDCK cells, not control mice; the source therefore does not support the claim's population or condition. (LLM, conf=0.88)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“In vivo, claudin-1 is essential for the epidermal water barrier (Furuse et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin contributes to epidermal barrier formation by regulating the incorporation of claudins into tight junctions
What the sources say
- Supportedcites Furuse et al, 2002 source
The Discussion reports that claudin-1–deficient newborn mice had a severely impaired epidermal barrier and excessive transepidermal water loss. It concludes that epidermal claudin-1 is indispensable for creating and maintaining that barrier. (LLM, conf=0.95)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“A previous paper did not reveal a lethal phenotype around birth in mice in which E-cadherin was deleted in the epidermis using K14-Cre (Tinkle et al, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
What the sources say
- Supportedcites Tinkle et al, 2004 source
The Results describe E-cadherin deletion in skin epithelium using K14-Cre and show newborn knockout pups. They also identify a full adult knockout mouse (Fig. 4), supporting the statement that the study did not reveal lethality around birth. Page numbers are unavailable in our copy. (LLM, conf=0.92)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“This paper, and another study, in which E-cadherin was inactivated in the epidermis after birth, showed a gradual loss of hair in the E-cadherin mutant mice (Young et al, 2003;Tinkle et al, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
What the sources say
- Supportedcites Young et al, 2003 source
In “Ablation of E-cadherin in the epidermis and hair follicles of mutant mice” (page not provided), E-cadherin was reduced after birth in mutant mice, followed by progressive hair loss. The paper reports that loss became evident after 30 days and continued into adulthood. (LLM, conf=0.94)
- Supportedcites Tinkle et al, 2004 source
The Results report sparse hair in adult E-cadherin mutant mice and describe progressive loss of hair follicles with successive postnatal hair cycles. The phrase about inactivation after birth describes the other study, not necessarily this one. (LLM, conf=0.89)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The E-cadherin gene was efficiently deleted from the epidermis of K14-Cre/Ecad Fl/À mice, as no RNA expression was observed (Figure 1B).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Generation of mice lacking E-cadherin in the epidermis
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- It may state two separate claims as one. 40
- Probably not a substantial claim. 35
Some cited sources support this claim and some don’t — read each source’s verdict below.
In the paper
“Both phenotypes are not observed in K14-Cre/Ecad Fl/À mice (Young et al, 2003;Tinkle et al, 2004;this paper).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Loss of E-cadherin does not result in loss or impairment of cell contact formation
What the sources say
- Partly supportedcites Young et al, 2003 sourceExperimental — accuracy not yet measured
The “Generation of conditional E-cadherin-deficient mice” section identifies the mutants as Krox20-Cre; E-cadherin ±/lox, not K14-Cre/Ecad Fl/−. The “Reduced proliferation in hair follicles” section reports no detected increase in epidermal proliferation in those mutants, but the paper does not establish the absence of both blistering and overgrowth in the K14-Cre genotype. (LLM, conf=0.76)
- Disputedcites Tinkle et al, 2004 sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) says older E-cadherin-null skin showed hyperproliferation and thickening, directly contrary to the claim that overgrowth was not observed. It also describes preservation of epidermal integrity, but that does not rescue the claim that neither phenotype occurred. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“For example, the tight junctional marker ZO-1 binds directly to a-catenin and this is considered an intermediate step in the formation of tight junctions (Itoh et al, 1997).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Supportedcites Itoh et al, 1997 source
The Discussion (page not provided) reports direct binding between ZO-1 and α-catenin. It also proposes that this interaction occurs early in epithelial junction formation, before ZO-1 may move from adherens junctions to tight junctions during maturation. The claim’s “considered” wording preserves that proposed, rather than established, sequence. (LLM, conf=0.86)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Claudin-1 is not a specific marker for tight junctions in the epidermis but, as described previously (Furuse et al, 2002), is found at the membrane of all epidermal layers in control mice (Figure 8A).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
What the sources say
- Supportedcites Furuse et al, 2002 source
In the Results section on occludin and claudins (Fig. 4A), the paper reports claudin-1 throughout the plasma membranes of wild-type epidermal keratinocytes from the basal through granular layers. It also notes that staining in the uppermost granular layer was fairly weak. (LLM, conf=0.90)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The association of E-cadherin with the actin cytoskeleton is mediated by a-catenin that is linked to the cadherin via b-catenin (Rimm et al, 1995).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Partly supportedcites Rimm et al, 1995 sourceExperimental — accuracy not yet measured
The Abstract (p. 8813) reports that α-catenin binds F-actin and that β-catenin can bind the α-catenin–actin complex. It proposes α-catenin as a tether at E-cadherin-mediated contacts, but does not establish the claimed β-catenin link to E-cadherin; it also presents the tethering mechanism as a model rather than a settled fact. (LLM, conf=0.85)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Interestingly, mice deficient for the tight junctional protein claudin-1 also show extensive water loss, appear red, shiny and wrinkled, and die within the same time frame as our mutant mice negative for E-cadherin in the epidermis (Furuse et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
What the sources say
- Partly supportedcites Furuse et al, 2002 sourceExperimental — accuracy not yet measured
The Results sections on postnatal lethality and epidermal barrier impairment report that claudin-1–deficient mice developed wrinkled skin, had excessive transepidermal water loss, and died within one day of birth (page unavailable). The paper does not describe them as red or shiny. The comparison with the citing authors’ E-cadherin mutants depends on the citing authors’ own findings, not this source. (LLM, conf=0.87)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In vitro studies have shown that E-cadherin is not only necessary for adherens junction formation but its adhesive activity is also crucial for the assembly of other junctional complexes such as desmosomes, gap junctions and tight junctions (Gumbiner et al, 1988;Musil et al, 1990;Watabe et al, 1994).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Partly supportedcites Gumbiner et al, 1988 sourceExperimental — accuracy not yet measured
The paper identifies uvomorulin as E-cadherin, and its discussion concludes that formation of adherens junctions, desmosomes, and tight junctions similarly depends on uvomorulin function. It does not address gap-junction assembly, so that part of the claim is unsupported by this source. The supplied passages do not give a page number for the discussion. (LLM, conf=0.88)
- Partly supportedcites Musil et al, 1990 sourceExperimental — accuracy not yet measured
The Results (p. 2083) show that disrupting L-CAM-mediated cell adhesion inhibits a change associated with functional gap junctions; the paper also reports that introducing L-CAM corrected a gap-junction communication defect. This supports a role for cell adhesion in gap-junction formation or function, but the cited paper does not establish the claimed necessity for adherens-junction formation or for assembly of desmosomes and tight junctions. (LLM, conf=0.86)
- Partly supportedcites Watabe et al, 1994 sourceExperimental — accuracy not yet measured
The study reports that activating E-cadherin in PC9 cells produced adherens junctions, tight junctions and desmosomes (p. 247), and its Discussion calls cadherin-mediated contact a prerequisite for forming the latter two (pp. 252–253). But it does not show that E-cadherin's adhesive activity is crucial for gap-junction assembly: the Introduction (p. 247) only says that introducing a cadherin into cadherin-deficient cells enhances gap-junction formation. (LLM, conf=0.85)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Indeed, experiments in Drosophila have shown that mutations in junctional proteins not only affect junction formation but also disturb epithelial polarity, whereas polarity mutants have a profound effect on junction formation as well (Cox et al, 1996;Muller and Wieschaus, 1996;Tanentzapf et al, 2000).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Supportedcites Cox et al, 1996 source
The discussion (p. 145) reports that embryos lacking the junctional protein Armadillo cannot assemble adherens junctions and lose epithelial cell polarity. The paper also states, in its discussion of epithelial development, that the bazooka and stardust gene products are essential for initial adherens-junction assembly, supporting the sentence’s point about polarity mutants. (LLM, conf=0.90)
- Supportedcites Muller and Wieschaus, 1996 source
The Abstract (p. 149) reports that stardust–bazooka mutants fail to form a zonula adherens and lose the organized epithelial cell layer. The Results (p. 158) report disrupted junction formation in embryos with reduced Armadillo, a junctional protein; the paper also describes their loss of the orderly monolayer. Together, these findings support both directions of the cited claim in Drosophila embryos. (LLM, conf=0.93)
- Supportedcites Tanentzapf et al, 2000 source
In Results (Role of the Cadherin–Catenin Complex in the Differentiation of the FE; page unavailable), the paper reports that disrupting adherens junctions in arm mutant follicle cells compromises both lateral and apical membrane domains. In Discussion (Activity of Apical, Lateral, and Basal Cues; page unavailable), it also reports prior findings that the apical polarity factor Crb is needed for zonula adherens formation in Drosophila embryos. Together, these support the two directions of the cited claim. (LLM, conf=0.89)
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“E-cadherin is important for tissue morphogenesis and polarity (Larue et al, 1994).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Supportedcites Larue et al, 1994 source
The Results and Discussion (page not provided) state that E-cadherin is central to early morphogenetic events and that its abundance is crucial for cell polarity and trophectoderm epithelial integrity. This supports the citing sentence’s broad paraphrase. (LLM, conf=0.93)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“However, such a model does not explain why specifically claudin-1, but not claudin-4 or occludin, is lacking from the granular layer whereas ZO-1 interacts with the C-terminus of all claudins and occludin (Fanning et al, 1998;Itoh et al, 1999).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Does aPKC play a role in E-cadherin-mediated epidermal tight junction formation?
What the sources say
- Partly supportedcites Fanning et al, 1998 sourceExperimental — accuracy not yet measured
The Results (page not provided) report that ZO-1 binds a fusion protein containing the C-terminal region of occludin. The paper does not report interactions with claudins, so it does not support the claim about all claudins. (LLM, conf=0.90)
- Partly supportedcites Itoh et al, 1999 sourceExperimental — accuracy not yet measured
The Results (page unavailable) show that ZO-1 binds the C-terminal regions of claudin-1 through claudin-8, which includes claudin-1 and claudin-4. The paper also reports binding between ZO-1 and the C-terminal tail of occludin. But it describes at least 16 claudin family members and does not establish binding to all of them. (LLM, conf=0.89)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“In addition, Rac activity has been implicated in the regulation of tight junction gate and fence function (Jou et al, 1998).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The small GTPase Rac may mediate E-cadherindependent localization of activated aPKC
What the sources say
- Supportedcites Jou et al, 1998 source
The Abstract states that Rac1 mutants perturbed tight junction gate function and disrupted fence function in MDCK cells. The Discussion section ‘TJ Gate and Fence Functions are Disrupted by RhoA and Rac1 Mutants’ likewise reports effects on both functions, supporting the citing sentence’s hedged claim. (LLM, conf=0.95)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Nevertheless, these authors did observe a slight disturbance in the epidermal barrier but have not examined tight junctional markers and function.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
What the sources say
- Partly supportedcites Tinkle et al, 2004 sourceExperimental — accuracy not yet measured
The Results report reduced filaggrin and loricrin in E-cadherin-null epidermis and say these changes were suggestive of a barrier defect that was likely mild. The paper does not report a direct barrier-function measurement, so “observed” overstates that inference. Its reported junctional analyses concern adherens junctions and desmosomes, not tight-junction markers or function. (LLM, conf=0.85)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“The discovery of tight junctions and their importance in the epidermal water barrier therefore came as a surprise (Brandner et al, 2002;Furuse et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin contributes to epidermal barrier formation by regulating the incorporation of claudins into tight junctions
What the sources say
- Not checked — no full text of the sourcecites Brandner et al, 2002 source
- Supportedcites Furuse et al, 2002 source
The Abstract says tight junctions had not been thought important to the mammalian epidermal barrier and calls the findings unexpected. It reports that claudin-1–deficient mice had severe transepidermal water loss and that continuous tight junctions were identified in the epidermis. The Discussion likewise contrasts this finding with the previously accepted emphasis on the cornified envelope and lipid lamellae. Page numbers are not provided in our copy. (LLM, conf=0.94)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
Every source the paper cites for this claim was checked and supports it.
In the paper
“This layer consists of dead keratin-filled cells embedded in a lipid matrix, thus providing a tough insoluble layer that separates the outside from the inside (Nemes and Steinert, 1999).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin contributes to epidermal barrier formation by regulating the incorporation of claudins into tight junctions
What the sources say
- Supportedcites Nemes and Steinert, 1999 source
The Introduction describes the cornified layer as keratin-rich corneocytes held together by intercorneocyte lipids and calls each cell’s envelope sturdy and extremely insoluble. The Abstract identifies these dead stratum corneum cells and their surrounding lipids as a barrier between the body and the environment. (LLM, conf=0.91)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Inactivation of a-catenin in the epidermis resulted in severe blistering and overgrowth (Vasioukhin et al, 2001).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Loss of E-cadherin does not result in loss or impairment of cell contact formation
What the sources say
- Partly supportedcites Vasioukhin et al, 2001 sourceExperimental — accuracy not yet measured
The discussion reports uncontrolled growth and large epidermal masses after α-catenin ablation, supporting the overgrowth claim. Figure 2 reports impaired intercellular junctions in the knockout epidermis, but the passages found do not report severe blistering; that part is unsupported. (LLM, conf=0.85)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Alternatively, growth regulation may be a cadherin-independent function of a-catenin (Vasioukhin et al, 2001).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Loss of E-cadherin does not result in loss or impairment of cell contact formation
What the sources say
- Partly supportedcites Vasioukhin et al, 2001 sourceExperimental — accuracy not yet measured
The Discussion (page unavailable in our copy) says α-catenin’s effects on hyperproliferation can be separated from its effects on cell–cell adhesion, supporting a possible growth-regulatory role beyond adhesion. But the paper also links the altered growth signaling to an E-cadherin/β-catenin complex with IRS-1; it does not establish that growth regulation is independent of cadherin itself. (LLM, conf=0.83)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In vitro studies using mostly simple epithelial cells have indicated that E-cadherin-mediated adhesion is a necessary prerequisite for the formation of other cell junctions, such as desmosomes, gap junctions and tight junctions (Gumbiner et al, 1988;Musil et al, 1990;Watabe et al, 1994).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin is specifically required for correct tight junction formation
What the sources say
- Partly supportedcites Gumbiner et al, 1988 sourceExperimental — accuracy not yet measured
The Abstract (p. 1575) reports that blocking uvomorulin, also identified as E-cadherin, similarly inhibited formation of desmosomes and tight junctions in cultured MDCK epithelial cells. It does not report testing gap junction formation, so that part of the citing sentence is not supported by this paper. (LLM, conf=0.88)
- Partly supportedcites Musil et al, 1990 sourceExperimental — accuracy not yet measured
The Results (p. 2083) show that introducing L-CAM into S180 cells increased gap-junction formation and communication, while disrupting L-CAM-mediated adhesion inhibited connexin43 processing. The Discussion says strong cell association *may* be important for gap-junction formation. The paper does not establish E-cadherin-mediated adhesion as a necessary prerequisite, or address desmosome and tight-junction formation as the claim states. (LLM, conf=0.87)
- Partly supportedcites Watabe et al, 1994 sourceExperimental — accuracy not yet measured
The Introduction (pp. 247–248) describes cadherins as prerequisites for epithelial junctional complexes, and the Discussion (p. 252) presents evidence that E-cadherin-mediated contact precedes tight-junction and desmosome formation. For gap junctions, however, the paper says cadherin introduction enhances their formation; it does not establish E-cadherin-mediated adhesion as necessary for them. (LLM, conf=0.84)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Indeed, staining for E-cadherin was negative in the newborn epidermis of mutant mice, whereas E-cadherin staining was found as expected in all layers of the epidermis in the skin of newborn control mice (Figure 1C).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Generation of mice lacking E-cadherin in the epidermis
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although its localization is still confined to the granular layer in K14-Cre/Ecad Fl/À mice, its distribution on the membrane is altered, showing a more punctate staining pattern.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The mutant skin appears more red and shiny than that of their control littermates, and has a parchmentlike resemblance.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Early deletion of E-cadherin in the epidermis results in perinatal death due to water loss
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Indeed, partial penetration of toluidine blue is observed around the paws and the ventral side in control E16.5 embryos and this pattern is similar for K14-Cre/Ecad Fl/À E16.5 embryos (Figure 6B).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The outside-in barrier is functional in K14-Cre/Ecad Fl/À mice
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This resulted in either K14-Cre/Ecad Fl/Fl or K14-Cre/Ecad Fl/À mice (Figure 1A) that both died within 1 day after birth.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Generation of mice lacking E-cadherin in the epidermis
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Differentiation markers and proliferation appeared normal (Supplementary Figure 2).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Cell-cell contacts are maintained in the absence of E-cadherin
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“P-cadherin expression is upregulated (Figure 2B) but was still mainly found in the basal layer of the epidermis of E-cadherin mutant mice (Figure 2A), suggesting that P-cadherin only compensates for the loss of Ecadherin in the basal layer.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Cell-cell contacts are maintained in the absence of E-cadherin
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Absence of E-cadherin leads to improper localization of key tight junctional proteins, resulting in permeable tight junctions and thus altered epidermal resistance.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Abstract
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Par3 is found at cell-cell contacts in all suprabasal layers of the epidermis, and its distribution (Figure 9A) and amount of protein (Figure 9B) were not significantly altered in K14-Cre/Ecad Fl/À mice.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“This fits with the observation that our mice lack whiskers despite the presence of hair follicles (not shown).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, E-cadherin loss did not alter the distribution of Par3, which is still found at sites of cell-cell contacts in the epidermis.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Does aPKC play a role in E-cadherin-mediated epidermal tight junction formation?
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although loss of E-cadherin does not result in absence of ZO-1 from the membrane, its distribution is dramatically altered, suggesting that it is no longer incorporated into tight junctions.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Does aPKC play a role in E-cadherin-mediated epidermal tight junction formation?
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Normal structure and cell-cell contacts in K14-Cre/Ecad Fl/À mice.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Rac activation assays
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, such a model does not explain why specifically claudin-1, but not claudin-4 or occludin, is lacking from the granular layer whereas ZO-1 interacts with the C-terminus of all claudins and occludin (Fanning et al, 1998;Itoh et al, 1999).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Does aPKC play a role in E-cadherin-mediated epidermal tight junction formation?
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Desmosomes are abundantly present in the absence of E-cadherin, and desmosomal markers appear to have their normal differentiation pattern within the epidermis.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin is specifically required for correct tight junction formation
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, this is perhaps unlikely in the upper layers of the epidermis, since Cdc42 expression appears to be confined to the basal layer and is not altered by the loss of E-cadherin.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The small GTPase Rac may mediate E-cadherindependent localization of activated aPKC
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Our results clearly show that loss of E-cadherin in the epidermis alters the permeability of tight junctions (Figure 7A) resulting in decreased epithelial resistance (Figure 7B).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin contributes to epidermal barrier formation by regulating the incorporation of claudins into tight junctions
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The activity of the Par3/Par6/aPKC polarity protein complex has been implicated in the formation of tight junctions in simple epithelia (Macara, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Macara, 2004 source
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Its activation depends on the formation of cell-cell contacts (Yamanaka et al, 2001) and Armadillo, the fly b-catenin homologue, is important for proper localization of this complex in Drosophila (Bilder et al, 2003;Tanentzapf and Tepass, 2003).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Yamanaka et al, 2001 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“The size and ion selectivity of tight junctions is variable within different tissues and depends on the type and levels of expression of claudins, four span transmembrane molecules, which constitute the tight junctional paired strands (Inai et al, 1999;Colegio et al, 2003).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Surprisingly, our results indicate that E-cadherin is specifically required for tight junction, but not desmosome, formation and this appears to involve signalling rather than cell contact formation.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Abstract
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Another catenin, p120 ctn , also binds directly to the cadherin and regulates the stability of the cadherin complex at the cell surface (Reynolds and Roczniak-Ferguson, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Reynolds and Roczniak-Ferguson, 2004 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Upon establishing cell-cell adhesion, cadherins cluster in specialized cell junctions, known as adherens junctions, which associate with the actin cytoskeleton (Gottardi et al, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not matchedcites Gottardi et al, 2002
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Not matched
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Overall, our results show that even though tight junction formation is not completely disturbed, key components are not properly incorporated, which likely underlies the functional impairment of tight junctions.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Activation of the Par3/Par6/aPKC complex is achieved by binding to the small GTPase Cdc42, resulting in the phosphorylation and activation of aPKC (Joberty et al, 2000;Lin et al, 2000).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“One of these polarity complexes consists of the Par3/ Par6/atypicalPKC (aPKC) complex, which localizes to the apical junctional complex in Drosophila and to tight junctions in mammalian epithelial cells (Nelson, 2003).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Nelson, 2003 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“This junctional complex assembly coincides with the establishment of cell polarity and enrichment at the cell junctions of several protein complexes known to be essential for polarity, suggesting an intimate relationship between junction formation and polarity (Nelson, 2003).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Nelson, 2003 source
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Two classical cadherins are expressed within the epidermis: P-cadherin, which is confined to the basal layer, and E-cadherin found in all epidermal cell layers (Jensen et al, 1997).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Jensen et al, 1997 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Its activation depends on the formation of cell-cell contacts (Yamanaka et al, 2001) and Armadillo, the fly b-catenin homologue, is important for proper localization of this complex in Drosophila (Bilder et al, 2003;Tanentzapf and Tepass, 2003).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Tight junctions act as selective permeability barriers but also form a fence that physically separates the apical membrane domain from the basolateral domain in simple epithelial cells (Anderson et al, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Anderson et al, 2004 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Desmosomes provide tissues with stable and strong cell-cell adhesion (Getsios et al, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Getsios et al, 2004 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This suggested that tight junctions are either absent or are no longer properly functioning in E-cadherin mutant skin.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We therefore conclude that maturation of the cornified layer developed normal in the absence of E-cadherin, resulting in a properly functioning outside-in barrier.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The outside-in barrier is functional in K14-Cre/Ecad Fl/À mice
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“In addition, claudin-6 overexpression in the skin also disturbs barrier function (Turksen and Troy, 2002).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Introduction
What the sources say
- Not checked — no full text of the sourcecites Turksen and Troy, 2002 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Experiments were repeated three times.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Rac activation assays
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, no differences in the levels of activated Rac were found between skin lysates of control and K14-Cre/ Ecad Fl/À mice (Figure 9C), suggesting that E-cadherin is important for the recruitment of activated Rac to sites of cell-cell contact but not for its activation per se.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Surprisingly, this effect is not due to a loss of cell contact formation or altered epidermal differentiation.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“It has been shown that Rac can bind to Par6 and thus potentially activate aPKC (Johansson et al, 2000;Lin et al, 2000).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The small GTPase Rac may mediate E-cadherindependent localization of activated aPKC
What the sources say
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Overall, an important implication of our work is that this effect of E-cadherin on tight junction formation is not simply the result of cell adhesion but rather seems to arise from signalling, most likely by recruitment of the small GTPase Rac and atypical PKC to sites of cell-cell contact.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin is specifically required for correct tight junction formation
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The increased expression of these two adhesive systems may explain why no blistering occurs and why cell contact formation appears normal in newborn epidermis (Figure 4).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Loss of E-cadherin does not result in loss or impairment of cell contact formation
hedgedconditional- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“In our K14-cre/Ecad Fl/À mice, E-cadherin is already almost completely absent at E15.5 (Figure 1C) shortly before the onset of barrier formation (Hardman et al, 1998), perhaps explaining why loss of E-cadherin has more dramatic consequences in our mice.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
What the sources say
- Not checked — no full text of the sourcecites Hardman et al, 1998 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, P-cadherin is only substantially upregulated in the basal layer in the absence of E-cadherin and it may require cadherin expression in the suprabasal layers to support tight junctions.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin is specifically required for correct tight junction formation
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Most data point to a role for Cdc42 as the small GTPase that activates the aPKC/Par3/Par6 complex (Macara, 2004).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The small GTPase Rac may mediate E-cadherindependent localization of activated aPKC
What the sources say
- Not checked — no full text of the sourcecites Macara, 2004 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We were unable to detect any obvious functional differences in the barrier function of the stratum corneum between control and K14-Cre/Ecad Fl/À mice, indicating that the cornified layer is not disturbed and still constitutes a functional barrier.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin contributes to epidermal barrier formation by regulating the incorporation of claudins into tight junctions
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, E-cadherin is essential for activation of aPKC at the appropriate localization or for recruitment of activated forms to sites of cell-cell contact.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Increased permeability of tight junctions in the absence of E-cadherin
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The upregulation of P-cadherin may also be sufficient to confer normal growth and differentiation properties to the basal epidermal keratinocytes in the absence of E-cadherin.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Loss of E-cadherin does not result in loss or impairment of cell contact formation
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Instead, we find that essential tight junctional components are not properly targeted to tight junctions, resulting in malfunctioning of these structures.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > Epidermal E-cadherin is essential for water barrier formation
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The ability to initiate and maintain cell-cell contacts is considered key to this E-cadherin function (Nelson, 2003).”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin is specifically required for correct tight junction formation
What the sources say
- Not checked — no full text of the sourcecites Nelson, 2003 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We propose that Rac may mediate E-cadherin-induced recruitment or activation of aPKC at cell-cell contacts in the epidermis.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > The small GTPase Rac may mediate E-cadherindependent localization of activated aPKC
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Claudins determine size and ion specificity of tight junctional barriers.”
§ E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions > E-cadherin contributes to epidermal barrier formation by regulating the incorporation of claudins into tight junctions
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Moreover, the TJ markers ZO-1 and occludin lost their continuous and linear apical distribution in Ecadepi−/− SG2. Instead, these proteins showed a more punctate pattern at cellular interfaces, revealing many breaks (Fig. 3d), thus explaining why in vivo TJ barrier function is disturbed upon loss of E-cadherin10.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Interestingly, this punctate intercellular contact pattern of ZO-1 and occludin was also observed in Ecadepi−/− spinous layers, indicating premature formation of non-functional TJ-like structures (Fig. 3d, f; Supplementary Fig. 3e; ref. 10).”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“A functional SC barrier is first formed in dorsal epidermis at embryonic day (E)16.5, spreading only to the ventral side one day later10, 20.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Interestingly, this increased activity was not associated with enhanced proliferation in vitro or in vivo (ref. 10; Supplementary Fig. 7g).”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In contrast, loss of vinculin in the epidermis did not affect either apical ZO-1 positioning or F-actin distribution in SG2 and did not result in major barrier defects in vivo, as vinculinepi−/− mice are viable, unlike Ecadepi−/− mice generated using the same K14-Cre line10.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
Experimental — accuracy not yet measured
The cited source says what the claim attributes to it.
In the citing paper
“In the epidermis loss of E-cadherin expressed in all viable layers interferes with the TJ barrier, resulting in perinatal death10.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
The cited source says what the claim attributes to it.
In the citing paper
“This was surprising as desmosomes, considered an important mechanical unit, are formed in these cells10, 23.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
The cited source says what the claim attributes to it.
In the citing paper
“In vivo, loss of epidermal vinculin did not result in perinatal lethality unlike loss of E-cadherin10.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“In conclusion, E-cadherin controls the polarized localization and activity status of suprabasal EGFR, which is uncoupled from growth10.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [10]
Experimental — accuracy not yet measured
Citations
Cites
Claudin-based tight junctions are crucial for the mammalian epidermal barrier
Furuse, M., Hata, M., Furuse, K., Yoshida, Y., Haratake, A., Sugitani, Y., Noda, T., Kubo, A., & Tsukita, S. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200110122 · Cited by 1,512
Fanning, A. S., Jameson, B. J., Jesaitis, L. A., & Anderson, J. M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.45.29745 · Cited by 1,432
Itoh, M., Furuse, M., Morita, K., Kubota, K., Saitou, M., & Tsukita, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.6.1351 · Cited by 1,151
E-cadherin null mutant embryos fail to form a trophectoderm epithelium.
Larue, L., Ohsugi, M., Hirchenhain, J., & Kemler, R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.17.8263 · Cited by 930
Self-citationThe cell-polarity protein Par6 links Par3 and atypical protein kinase C to Cdc42
Joberty, G., Petersen, C., Gao, L., & Macara, I. G. (2000) · Nature Cell Biology · doi:10.1038/35019573 · Cited by 928
Gumbiner, B., Stevenson, B., & Grimaldi, A. (1988) · The Journal of cell biology · doi:10.1083/jcb.107.4.1575 · Cited by 799
A mammalian PAR-3–PAR-6 complex implicated in Cdc42/Rac1 and aPKC signalling and cell polarity
Lin, D., Edwards, A. S., Fawcett, J. P., Mbamalu, G., Scott, J. D., & Pawson, T. (2000) · Nature Cell Biology · doi:10.1038/35019582 · Cited by 743
Rimm, D. L., Koslov, E. R., Kebriaei, P., Cianci, C. D., & Morrow, J. S. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8813 · Cited by 735
Pérez‐Moreno, M., Jamora, C., & Fuchs, E. V. (2003) · Cell · doi:10.1016/s0092-8674(03)00108-9 · Cited by 717
Adaptation of core mechanisms to generate cell polarity
Nelson, W. J. (2003) · Nature · doi:10.1038/nature01602 · Cited by 716
Research works printed but not linked: 1
- Gottardi CJ, Niessen CM, Gumbiner BM (2002) The adherens junction. In Cell Adhesion, The Frontiers in Molecular Biology Series, Hames BD, Glover DM, Beckerle M (eds). chap 8, Oxford University Press
Cited by
Sorted by citations
Items 201–300 of 491
Lee, H. Y., Choi, J., Hong, J. W., et al. (2018) · Journal of Physics D Applied Physics · doi:10.1088/1361-6463/aabd8c · Cited by 34
“E-cadherin is one of the key-player proteins for maintaining the skin barrier function [32].”
BackgroundTrans-Compartmental Regulation of Tight Junction Barrier Function
Naser, A. N., Lu, Q., & Chen, Y. (2022) · Tissue Barriers · doi:10.1080/21688370.2022.2133880 · Cited by 42
Somatostatin regulates tight junction function and composition in human keratinocytes
Vockel, M., Breitenbach, U., Kreienkamp, H., & Brandner, J. M. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2010.01101.x · Cited by 36
Swadźba, E., & Rupik, W. (2010) · Zoology · doi:10.1016/j.zool.2010.07.002 · Cited by 34
Song, J., Zhao, H., Dong, H., Zhang, D., Zou, M., Tang, H., Liu, L., Liang, Z., Lv, Y., Zou, F., et al. (2013) · Toxicology Letters · doi:10.1016/j.toxlet.2013.03.033 · Cited by 35
Cell-Cell Adhesions and Cell Contractility Are Upregulated upon Desmosome Disruption
Sumigray, K., Zhou, K., & Lechler, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101824 · Cited by 32
Expansive Generation of Functional Airway Epithelium From Human Embryonic Stem Cells
McIntyre, B. A. S., Alev, C., Mechael, R., Salci, K. R., Lee, J. B., Fiebig‐Comyn, A., Guezguez, B., Wu, Y., Sheng, G., & Bhatia, M. (2013) · Stem Cells Translational Medicine · doi:10.5966/sctm.2013-0119 · Cited by 34
Prevention of tumor growth by needle-free jet injection of anti-C7orf24 siRNA
Hama, S., Arata, M., Nakamura, I., Kasetani, T., Itakura, S., Tsuchiya, H., Yoshiki, T., & Kogure, K. (2012) · Cancer Gene Therapy · doi:10.1038/cgt.2012.31 · Cited by 33
Zhang, M., Wang, X., Guo, F., Jia, Q., Liu, N., Chen, Y., Yan, Y. C., Huang, M., Tang, H., Deng, Y., et al. (2019) · Theranostics · doi:10.7150/thno.34014 · Cited by 32
“Considering that loss of E-cadherin, ZO-1 and desmoplakin alone can cause neonatal death and epidermal barrier damage [52-54], alterations in these proteins may have resulted in inside-out barrier defects in Cdc42 KO mice.”
BackgroundPKC-δ binds to E-cadherin and mediates EGF-induced cell scattering
Singh, R., Lei, P., & Andreadis, S. T. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.07.002 · Cited by 33
“Interestingly, occludin also binds to α-catenin [20], while E-cadherin is required for the formation of functional tight junctions in vivo [21].”
Wakamatsu, K., Ogita, H., Okabe, N., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611159200 · Cited by 33
Hereditary barrier-related diseases involving the tight junction: lessons from skin and intestine
Brandner, J. M., & Schulzke, J. D. (2015) · Cell and Tissue Research · doi:10.1007/s00441-014-2096-1 · Cited by 34
Epidermal Polarity Genes in Health and Disease
Tellkamp, F., Vorhagen, S., & Niessen, C. M. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a015255 · Cited by 33
Self-citationYang, L., Lin, Z., Mu, R., Wu, W., Zhi, H., Liu, X., Yang, H., & Liu, L. (2024) · eLife · doi:10.7554/elife.96161.3 · Cited by 34
Liu, Y., Wu, J., Wu, J., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.155292 · Cited by 32
Ali, N., Gomes, M., Bauer, R., Brodesser, S., Niemann, C., & Iden, S. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.07.011 · Cited by 32
“While barrier-promoting functions of Par3 outside TJ regulation are also conceivable, such an inside-out barrier defect is reminiscent of global cl udin-1 (Furuse et al, 2002) and epidermal E-cadherin deletion (Tunggal et al. 2005), supporting he idea of Par3 as regulator of the in vivo TJ barrier.”
BackgroundWang, X., Li, L., & Zhang, G. (2020) · Food & Function · doi:10.1039/d0fo01579b · Cited by 32
Yao, L., Zhao, H., Tang, H., et al. (2015) · Toxicological Sciences · doi:10.1093/toxsci/kfv120 · Cited by 32
“They display a highly regulated and impermeable barrier through the formation of tight junctions (TJs) and adherens junctions (AJs), which consist of E-cadherin, b-catenin, and a-catenin (Nawijn et al., 2011). bCatenin links E-cadherin at the plasma membrane to a-catenin (Takeichi, 1995).”
BackgroundInfluentialYuan, J., Shen, Y., Yang, X., et al. (2017) · BMC Nephrology · doi:10.1186/s12882-017-0708-1 · Cited by 32
“Lower levels of E-cadherin also reflect the early changes observed during epithelialmesenchymal transition(EMT) [25, 26].”
BackgroundEsrp1-Regulated Splicing of Arhgef11 Isoforms Is Required for Epithelial Tight Junction Integrity
Lee, S., Cieply, B. W., Yang, Y., Peart, N. J., Glaser, C., Chan, P., & Carstens, R. P. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.097 · Cited by 28
“The water loss phenotype and alterations in TJ markers in Esrp1−/−;Esrp2−/− pups suggested an “inside-out” permeability defect similar to other mouse models associated with defective TJs (Furuse et al., 2002; Gladden et al., 2010; Tunggal et al., 2005).”
BackgroundResultInfluentialTight Junction Proteins in Gallbladder Epithelium
Laurila, J. J., Karttunen, T. J., Koivukangas, V., Laurila, P., Syrjälä, H., Saarnio, J., Soini, Y., & Ala-Kokko, T. I. (2007) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.6a7155.2007 · Cited by 32
“Epithelial expression of junctional proteins was investigated as follows: claudin-1, -2, -3, and -4, occludin, and ZO-1 as elements of TJs, and E-cadherin as an element of adherens junctions.”
BackgroundInfluentialRahn, E., Thier, K., Petermann, P., Rübsam, M., Staeheli, P., Iden, S., Niessen, C. M., & Knebel-Mörsdorf, D. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.11.027 · Cited by 31
Self-citationAltered CD40 and E‐cadherin expression – putative role in oral lichen planus
Neppelberg, E., Loro, L. L., Øijordsbakken, G., et al. (2007) · Journal of Oral Pathology and Medicine · doi:10.1111/j.1600-0714.2007.00511.x · Cited by 31
Enhanced differentiation of embryonic stem cells using co‐cultivation with hepatocytes
Moore, R. N., Dasgupta, A., Rajaei, N., Yarmush, M. L., Toner, M., Larue, L., & Moghe, P. V. (2008) · Biotechnology and Bioengineering · doi:10.1002/bit.21987 · Cited by 31
“In particular, tight junction (Loreal et al., 1993; Tunggal et al., 2005) and gap junction (Mesnil et al.”
BackgroundChami, C. E., Foster, A. R., Johnson, C., Clausen, R. P., Cornwell, P. A., Haslam, I. S., Steward, M. C., Watson, R. E. B., Young, H. S., & O’Neill, C. A. (2020) · British Journal of Dermatology · doi:10.1111/bjd.19162 · Cited by 30
Identification of a novel dual E- and N-cadherin antagonist
Devemy, E., & Blaschuk, O. W. (2009) · Peptides · doi:10.1016/j.peptides.2009.05.010 · Cited by 30
HGF-Induced PKCζ Activation Increases Functional CXCR4 Expression in Human Breast Cancer Cells
Huang, S., Ouyang, N., Lin, L., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029124 · Cited by 30
Serum response factor is essential for the proper development of skin epithelium
Verdoni, A. M., Ikeda, S., & Ikeda, A. (2010) · Mammalian Genome · doi:10.1007/s00335-009-9245-y · Cited by 29
“…deficient for E-cadherin display phenotypes similar to those of claudin 1-deficient mice in addition to aberrant localization of tight junction proteins, demonstrating that E-cadherin is essential for the inside-out epidermal barrier through its regulation of tight junctions (Tunggal et al. 2005).”
InfluentialTatari, M. N., Craene, B. D., Soen, B., et al. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1589-0 · Cited by 29
Nin, V., Hernández, J. A., & Chifflet, S. (2009) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20416 · Cited by 29
Li, F., Pascal, L. E., Stolz, D. B., et al. (2019) · The Prostate · doi:10.1002/pros.23806 · Cited by 29
Yao, D., Alexander, C. L., Quinn, J. A., Porter, M., Wu, H., & Greenhalgh, D. A. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-2341 · Cited by 29
“Failure of E-cadherin-mediated adhesion resulted in a lethal neonatal phenotype of barrier dysfunction (46); thus, if PTEN was critical for E-cadherin function(s), then a default terminal differentiation program would be a logical mechanism to deploy following PTEN loss to counter proliferation and the dangers of a co…”
BackgroundInterleukin 9 Alters Epithelial Barrier and E‐cadherin in Eosinophilic Esophagitis
Doshi, A., Khamishon, R., Rawson, R., et al. (2018) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000002144 · Cited by 28
“Interestingly, E-cadherin is essential for barrier function as well as proper epithelial stratification and flattening of cell morphology in the skin (27,28).”
Baek, J. H., Lee, S. E., Choi, K. J., Choi, E. H., & Lee, S. H. (2013) · Yonsei Medical Journal · doi:10.3349/ymj.2013.54.2.523 · Cited by 30
Tight junctions form a barrier in porcine hair follicles
Mathes, C., Brandner, J. M., Laue, M. M., Raesch, S. S., Hansen, S., Failla, A. V., Vidal‐y‐Sy, S., Moll, I., Schaefer, U. F., & Lehr, C. (2015) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2015.12.001 · Cited by 28
Niessen, M. T., Iden, S., & Niessen, C. M. (2012) · Journal of Cell Science · doi:10.1242/jcs.092890 · Cited by 30
“In addition, loss of cell adhesion molecules, such as E-cadherin (Tunggal et al., 2005) or CD44 (Kirschner et al.”
BackgroundSelf-citationCelli, A., Tu, C., Lee, E., et al. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2021.03.025 · Cited by 28
Hafa, L., Breideband, L., Posada, L., Torras, N., Martínez, E., Stelzer, E. H. K., & Pampaloni, F. (2023) · Advanced Materials · doi:10.1002/adma.202306258 · Cited by 34
Zhang, W., Chen, Y. X., Li, M., Cao, S., Wang, N., Zhang, Y., & Wang, Y.-T. (2023) · Advanced Science · doi:10.1002/advs.202302855 · Cited by 25
N-cadherin expression level as a critical indicator of invasion in non-epithelial tumors
Péglion, F., & Etienne‐Manneville, S. (2012) · Cell Adhesion & Migration · doi:10.4161/cam.20855 · Cited by 29
Hu, Y., Dong, H., Zou, M., et al. (2017) · Cellular Immunology · doi:10.1016/j.cellimm.2017.02.003 · Cited by 27
“E-cadherin connects adjacent cells and controls the outcome of the response to allergens through its interaction with Tregs and DCs [5,6].”
BackgroundCdc42 expression in keratinocytes is required for the maintenance of the basement membrane in skin
Wu, X., Quondamatteo, F., & Brakebusch, C. (2006) · Matrix Biology · doi:10.1016/j.matbio.2006.09.001 · Cited by 27
HER2 activation results in β-catenin-dependent changes in pulmonary epithelial permeability
Finigan, J. H., Vasu, V. T., Thaikoottathil, J., Mishra, R., Shatat, M. A., Mason, R. J., & Kern, J. A. (2014) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00237.2014 · Cited by 26
The Western-Style Diet, Calcium Deficiency and Chronic Disease
Aslam, M. N., & Varani, J. (2016) · Journal of Nutrition & Food Sciences · doi:10.4172/2155-9600.1000496 · Cited by 27
The impact of manganese on vascular endothelium
Oliveira‐Paula, G. H., Martins, A. C., Ferrer, B., Tinkov, A. A., Skalny, A. V., & Aschner, M. (2024) · Toxicological Research · doi:10.1007/s43188-024-00260-1 · Cited by 26
MicroRNA profiling in cutaneous wounds of diabetic rats
Liu, Y.-F., Ding, M., Liu, D.-W., Liu, Y., Mao, Y., & Peng, Y. (2015) · Genetics and Molecular Research · doi:10.4238/2015.august.14.24 · Cited by 25
“, 2008) and thus was seemed to be essential in maintaining epithelial stability (Tunggal et al., 2005), suggesting that it has an inhibitory effect on diabetic wound healing.”
BackgroundTopical tranexamic acid improves the permeability barrier in rosacea
Zhong, S., Sun, N., Liu, H., et al. (2015) · Dermatologica Sinica · doi:10.1016/j.dsi.2015.04.012 · Cited by 25
“23,24 Inhibition of SP by tranexamic Table 1 Lesion assessment of rosacea patients before and after treatment.”
BackgroundDesmoglein2 Regulates Claudin2 Expression by Sequestering PI-3-Kinase in Intestinal Epithelial Cells
Burkard, N., Meir, M., Kannapin, F., Otto, C., Petzke, M., Germer, C., Waschke, J., & Schlegel, N. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.756321 · Cited by 27
ABCH2 transporter mediates deltamethrin uptake and toxicity in the malaria vector Anopheles coluzzii
Kefi, M., Balabanidou, V., Sarafoglou, C., Charamis, J., Lycett, G. J., Ranson, H., Gouridis, G., & VONTAS, J. G. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011226 · Cited by 24
Mao, X., Li, P., Ren, Y. T., Li, J., Zhou, C., Yang, J., & Liu, P. (2014) · International Journal of Oncology · doi:10.3892/ijo.2014.2763 · Cited by 24
An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
Jahanshahi, M., Hamdi, D., Godau, B., Samiei, E., Sánchez-Lafuente, C. L., Neale, K. J., Hadisi, Z., Dabiri, S. M. H., Pagan, E., Christie, B. R., et al. (2020) · Micromachines · doi:10.3390/mi11020227 · Cited by 26
Törmä, H., & Berne, B. (2009) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.00877.x · Cited by 24
The role of secreted Hsp90α in HDM-induced asthmatic airway epithelial barrier dysfunction
Ye, C., Huang, C., Zou, M., et al. (2019) · BMC Pulmonary Medicine · doi:10.1186/s12890-019-0938-z · Cited by 24
Stemmler, M. P., & Bedzhov, I. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22375 · Cited by 25
Pores in the epidermis: aquaporins and tight junctions
Brandner, J. M. (2007) · International Journal of Cosmetic Science · doi:10.1111/j.1468-2494.2007.00402.x · Cited by 24
“Also epidermis-specific E-cadherin knock out mice die soon after birth because of a tremendous TEWL and exhibit leaky TJ [72].”
Hung, C., Chen, W., Aljuffali, I. A., Shih, H.-C., & Fang, J. (2014) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2014.05.034 · Cited by 24
Xiong, L., Lin, T., Yue, X., Zhang, S., Liu, X., Chen, F., Zhang, S., & Guan, W. (2023) · Antioxidants · doi:10.3390/antiox12122064 · Cited by 23
E-cadherin roles in animal biology: A perspective on thyroid hormone-influence
Izaguirre, M. F., & Casco, V. H. (2016) · Cell Communication and Signaling · doi:10.1186/s12964-016-0150-1 · Cited by 22
Weikard, R., Hadlich, F., Hammon, H. M., Frieten, D., Gerbert, C., Koch, C., Dusel, G., & Kuehn, C. (2018) · Oncotarget · doi:10.18632/oncotarget.24898 · Cited by 23
“Several genes acting in this pathway including CDH1 and CTNND1, which play a critical role in formation of adherens and tight junctions and influence membrane surface stability [54], were sligthly lower expressed in RES compared to AL calves.”
Chamseddine, D., Mahmud, S. A., Westfall, A. K., Castoe, T. A., Berg, R. E., & Pellegrino, M. W. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111789 · Cited by 21
“70 Disruptions to intestinal barrier function are a hallmark of inflammatory bowel diseases (IBD), including Crohn disease and ulcerative colitis.”
Fungal Aeroallergens—The Impact of Climate Change
Sztandera−Tymoczek, M., & Szuster‐Ciesielska, A. (2023) · Journal of Fungi · doi:10.3390/jof9050544 · Cited by 23
Jia, L., Liu, X., Liu, X., Guan, Q., Tian, Y., Li, J., & Zhao, P. (2024) · Chinese Medicine · doi:10.1186/s13020-024-00905-1 · Cited by 22
“Furthermore, the ERK1/2 inhibitor U0126 and EGFR inhibitor AG1478 significantly inhibit TJ dissociation and DNA damage [32].”
BackgroundTCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
Fehrenschild, D., Galli, U., Breiden, B., Bloch, W., Schettina, P., Brodesser, S., Michels, C., Günschmann, C., Sandhoff, K., Niessen, C. M., et al. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.301 · Cited by 22
“Tight-junction barrier is not impaired by mutant Lef1 It was previously reported that the outside-in barrier function was not obviously disturbed in mice with impaired tight junctions that suffered from water loss (Furuse et al., 2002; Tungal et al., 2005).”
BackgroundSelf-citationScaffolding proteins in the development and maintenance of the epidermal permeability barrier
Crawford, M., & Dagnino, L. (2017) · Tissue Barriers · doi:10.1080/21688370.2017.1341969 · Cited by 21
“Targeted inactivation of Cdh1 in mice, which encodes E-cadherin, results in extensive transepidermal water loss and loss of functional tight junctions in the stratum granulosum.(63) In these mice, paracellular diffusion of ions was also increased due to enhanced tight junction permeability.”
BackgroundOzawa, M., & Kobayashi, W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105313 · Cited by 21
Macartney, R. A., Das, A., Imaniyyah, A. G., Fricker, A. T. R., Smith, A. M., Fedele, S., Roy, I., Kim, H., Lee, D., & Knowles, J. C. (2025) · Journal of Tissue Engineering · doi:10.1177/20417314241313458 · Cited by 26
“203 Therefore, it is a reasonable assumption that the barrier function is reduced by C. albicans infection.”
Mellas, R. E., Leigh, N. J., Nelson, J. W., et al. (2014) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155414555145 · Cited by 21
“E-cadherin supports cell–cell adhesion and can affect a wide range of cellular functions, including activation of cell signaling pathways, regulation of the cytoskeleton and control of cell polarity (Larue et al. 1994; Tunggal et al. 2005).”
BackgroundInfluentialNeonatal Injury Increases Gut Permeability by Epigenetically Suppressing E-Cadherin in Adulthood
Kline, K. T., Lian, H., Zhong, X. S., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900639 · Cited by 21
“This includes E-cadherin, an essential adherens junction protein that is also required for tight junction formation (2).”
BackgroundThree-Dimensional Aggregated Spheroid Model of Hepatocellular Carcinoma Using a 96-Pillar/Well Plate
Lee, S., Teng, Y. H.-F., Son, M., Ku, B., Hwang, H. J., Tergaonkar, V., Chow, P. K. H., Lee, D. W., & Nam, D. (2021) · Molecules · doi:10.3390/molecules26164949 · Cited by 21
“Previously ZO-1 alternation made the different drug resistance [25].”
BackgroundZwaans, B. M. M., Carabulea, A. L., Bartolone, S. N., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-98303-2 · Cited by 21
Xin, Y., Wen, X., Hamblin, M. R., et al. (2020) · Journal of Cosmetic Dermatology · doi:10.1111/jocd.13581 · Cited by 20
To Stick or Not to Stick: Adhesions in Orofacial Clefts
Antiguas, A., Paul, B. J., & Dunnwald, M. (2022) · Biology · doi:10.3390/biology11020153 · Cited by 23
Granzyme B in epithelial barrier dysfunction and related skin diseases
Jung, K., Pawluk, M. A., Lane, M. D., Nabai, L., & Granville, D. J. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00052.2022 · Cited by 22
Muenyi, C. S., Carrion, S. L., Jones, L. A., Kennedy, L. H., Slominski, A. T., Sutter, T. R., & Sutter, T. R. (2014) · Environmental Health Perspectives · doi:10.1289/ehp.1308045 · Cited by 20
“Several animal studies have reported that mice with defective TJs have compromised EPB function and show enhanced TEWL (Furuse et al. 2002; Sugawara et al. 2013; Tunggal et al. 2005; Turksen and Troy 2002).”
BackgroundCadherin‐Mediated Regulation of Tight Junctions in Stratifying Epithelia
Michels, C., Aghdam, S. Y., & Niessen, C. M. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04443.x · Cited by 20
Self-citationHernández-Padilla, L., de la Cruz, H. R., & Campos‐García, J. (2020) · APOPTOSIS · doi:10.1007/s10495-020-01619-z · Cited by 19
Qian, G., Zang, H., Tang, J., Zhang, H., Yu, J., Jia, H., Zhang, X., & Zhou, J. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012541 · Cited by 20
Role of E-Cadherin in Epithelial Architecture Maintenance
Izaguirre, M. F., Larrea, D., Adur, J. F., Zamboni, J. E. D., Vicente, N. J. R., Galetto, C. D., & Casco, V. H. (2010) · Cell Communication & Adhesion · doi:10.3109/15419061003686938 · Cited by 19
“cell polarity set up in cell junctions, such as E-cadherin and associated proteins (Lecuit 2005; Tunggal et al. 2005; Classen et al. 2005; Wang and Nathan 2007).”
BackgroundInfluentialWang, Y., Xu, Y., Yan, W., Han, P., Liu, J., Gong, J., Li, D., Ding, X., Wang, H., Lin, Z., et al. (2018) · Oncotarget · doi:10.18632/oncotarget.24364 · Cited by 19
“The EMT is a reversible and dynamic process that allows the transition between the epithelial and the mesenchymal phenotype during tissue development and repair.”
BackgroundInfluentialFerroptosis mediates airway epithelial E-cadherin dysfunction in LPS-induced acute lung injury
Chen, Z., Tang, H., Gan, S., Yang, C., Li, S., Li, J., & Yao, L. (2023) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2023.102284 · Cited by 18
Simard‐Bisson, C., Bidoggia, J., Larouche, D., Guérin, S. L., Blouin, R., Hirai, S.-I., & Germain, L. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.07.035 · Cited by 19
“DISCUSSION Cell-cell junctions are essential for tissue cohesion and skin barrier function (Furuse and Tsukita, 2006; Tunggal et al., 2005).”
BackgroundSmyth, T., & Georas, S. N. (2021) · Inhalation Toxicology · doi:10.1080/08958378.2021.1956021 · Cited by 19
“In knockout mouse models, E-cadherin null mice exhibited embryonic lethality [79] and inducible post-natal knockout mice were shown to exhibit high levels of epidermal water loss [80,81].”
BackgroundImproving disease prevention, diagnosis, and treatment using novel bionic technologies
Manero, A. C., Crawford, K. E., Gibbs, H. P., Shah, N., Gandhi, D. A., & Coathup, M. J. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10359 · Cited by 18
“essential for in vivo epidermal barrier function.(85) Promising preliminary results have also been demonstrated in patients.”
BackgroundWanat, K. A., Rosenbach, M. A., Zoiber, A. F., Zhang, P. J., & Schaffer, A. (2013) · American Journal of Dermatopathology · doi:10.1097/dad.0b013e31828de7e0 · Cited by 18
“E-cadherin, an epithelial cadherin, is critical in epidermal barrier function by regulating the formation of tight junctions between keratinocytes.(11) E-cadherin expression has also been observed in CD1a+ Langerhans cells (LCs) in the epidermis, where it is thought to enhance heterotypic adhesion between LCs and kera…”
Epidermal RAF prevents allergic skin disease
Raguz, J., Jerić, I., Niault, T., Nowacka, J. D., Kužet, S.-E., Rupp, C., Fischer, I., Biggi, S., Borsello, T., & Baccarini, M. (2016) · eLife · doi:10.7554/elife.14012 · Cited by 19
“Water loss assay and toluidine blue dye staining of embryos were carried out as described (Tunggal et al., 2005).”
MethodTooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
Naveau, A., Seidel, K., & Klein, O. D. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.02.003 · Cited by 19
“Epithelial (E)-cadherin is a cell–cell junctional protein essential in promoting morphogenesis and maintaining skin and its appendages [64,65].”
BackgroundCytokine Regulation during Epidermal Differentiation and Barrier Formation
Tsuchisaka, A., Furumura, M., & Hashimoto, T. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.15 · Cited by 17
IRF6 Regulates the Delivery of E-Cadherin to the Plasma Membrane
Antiguas, A., DeMali, K. A., & Dunnwald, M. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2021.06.031 · Cited by 17
Biophysical Methods to Study Tight Junction Permeability
(2010) · Current topics in membranes · doi:10.1016/s1063-5823(10)65003-x · Cited by 17
Basilicata, M. F., Frank, M., Solter, D., Brabletz, T., & Stemmler, M. P. (2016) · Scientific Reports · doi:10.1038/srep26562 · Cited by 17
“Lack of E-cad results in defects in trophec-toderm integrity of the blastocyst, in mammary gland, placenta and skin homeostasis 1–4 , 38 .”
Hsu, C., Lecland, N., Pendaries, V., Viodé, C., Redoules, D., Paul, C. F., Merdes, A., Simon, M., & Bierkamp, C. (2018) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2018.04.008 · Cited by 17
Prasad, K., Sasi, S., Weerasinghe, J., Levchenko, I., & Bazaka, K. (2023) · Molecules · doi:10.3390/molecules28227481 · Cited by 19
Blood Vessel Epicardial Substance (BVES) in junctional signaling and cancer
Parang, B., Thompson, J. J., & Williams, C. S. (2018) · Tissue Barriers · doi:10.1080/21688370.2018.1499843 · Cited by 16
“Interestingly, disruption of E-cadherin in the epidermis leads to alterations in the tight junction, highlighting the interconnectivity of the junctional barrier network.(10) Indeed, tight junctions are often in close association with adherens junctions near the apical-lateral membrane and help to form a selective, se…”
BackgroundCianfarani, F., Bernardini, S., Luca, N. D., Dellambra, E., Tatangelo, L., Tiveron, C., Niessen, C. M., Zambruno, G., Castiglia, D., & Odorisio, T. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.137 · Cited by 16
“Rac activation assay Rac activation was analyzed on cultured keratinocytes treated for 1 hour with 100 ng ml 1 of rmIGF-1 (Peprotech) following the procedure described by Tunggal et al. (2005) and using an anti”
MethodSelf-citationChaudhuri, R. K., & Bojanowski, K. (2017) · International Journal of Cosmetic Science · doi:10.1111/ics.12405 · Cited by 16
“Besides supporting cell–cell adhesion, cadherins can affect a wide range of cellular functions that include activation of cell signalling pathways, regulation of the cytoskeleton and control of cell polarity [17].”
BackgroundColl, T. A., Pérez‐Tito, L., Sobarzo, C., & Cebral, E. (2011) · Birth Defects Research Part B Developmental and Reproductive Toxicology · doi:10.1002/bdrb.20329 · Cited by 16
Force Measurement Tools to Explore Cadherin Mechanotransduction
Stapleton, S. C., Chopra, A., & Chen, C. S. (2014) · Cell Communication & Adhesion · doi:10.3109/15419061.2014.905929 · Cited by 15
“…of cell – cell contacts but also crucial for initiating and dynamically regulating the formation of other cell junctional complexes such as tight and gap junctions, and desmosomes (Gumbiner et al., 1988; Tunggal et al., 2005; Frenzel & Johnson, 1996; Lewis et al., 1994; Capaldo & Macara, 2007).”
Reconstructing the epidermal proteolytic cascades in health and disease
Sotiropoulou, G., Zingkou, E., & Pampalakis, G. (2022) · The Journal of Pathology · doi:10.1002/path.5888 · Cited by 15
“Cst6 / Mice display compact orthokeratotic scales and die from P5 to P12 due to impaired barrier [73] Cdsn / Mice recapitulate peeling skin syndrome (PSD) and die within a few hours from birth [74] Cdsn / Mice recapitulate peeling skin syndrome (PSD) and die within a few hours from birth [75] Cdsn / Inducible conditio…”
BackgroundShin, D.-Y., Yoon, M.-K., Choi, Y. W., et al. (2010) · Journal of Life Science · doi:10.5352/jls.2010.20.4.528 · Cited by 15
“이와 같이 TJ 단백질은 아울러 TJ 관련단 백질(E-cadherin, Snail 등)들과의 상호 작용을 통하여 암세포 의 전이를 조절할 수 있다[8,23,25,26].”
InfluentialCarvalho, A., de Souza, W., & Morgado‐Díaz, J. A. (2006) · International Journal of Radiation Biology · doi:10.1080/09553000600930095 · Cited by 16
“These interactions permit an efficient transduction of signals from TJ and AJ to the cell interior as well as from cytosolic compartments to TJ and AJ (Matter & Balda 2003, Erez et al. 2005, Tunggal et al. 2005).”
Background
Metadata
- Authors
- Tunggal, J. A., Helfrich, I., Schmitz, A., Schwarz, H., Günzel, D., Fromm, M., Kemler, R., Krieg, T., & Niessen, C. M.
- Affiliations
- University of Cologne (DE)
- Max Planck Institute for Developmental Biology (DE)
- Stiftung Charité (DE)
- Max Planck Society (DE)
- Corresponding author
- Niessen, Carien M
- Venue
- The EMBO Journal
- Published
- 2005-03-03
- Volume
- 24
- Issue
- 6
- Pages
- 1146-1156
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC556407
- OpenAlex
- W2145470537
- Semantic Scholar
- a188609a53de11c26fa2a5f349e10e9c4ff65cab
- Cited by
- 491
- References
- 53
- Citations by year
- 2026: 23 · 2025: 23 · 2024: 23 · 2023: 21 · 2022: 18 · 2021: 23 · 2020: 23 · 2019: 21 · 2018: 22 · 2017: 25 · 2016: 26 · 2015: 28 · 2014: 32 · 2013: 22 · 2012: 29
- FWCI
- 11.27
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- The EMBO Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Digital Library (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Northwestern University
- Deutsches Krebsforschungszentrum
- Deutsche Forschungsgemeinschaft (SFB589)
- Universität zu Köln
- University of North Carolina at Chapel Hill
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Keywords
- E-cadherin, skin barrier function, tight junctions, desmosomes, stratified epithelium, conditional gene inactivation, epidermal permeability, Rac, atypical protein kinase C, perinatal lethality, cell adhesion
- MeSH terms
- Animals, Cell Communication, Desmosomes, Epidermis, Genes, Lethal, Membrane Proteins, Mice, Transgenic, Protein Kinase C, Water, Cadherins, Gene Deletion, Tight Junctions, rac GTP-Binding Proteins, Mice
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