The DOI matches its Crossref record; 95 of the 95 references it cites were found in a registry or an index; 28 of the 38 sources its claims cite were checked for support.
APOE4-specific Changes in Aβ Accumulation in a New Transgenic Mouse Model of Alzheimer Disease
Open accessAbstract
APOE4 is the greatest risk factor for Alzheimer disease (AD) and synergistic effects with amyloid-β peptide (Aβ) suggest interactions among apoE isoforms and different forms of Aβ accumulation. However, it remains unclear how the APOE genotype affects plaque morphology, intraneuronal Aβ, soluble Aβ42, and oligomeric Aβ (oAβ), particularly in vivo. As the introduction of human APOE significantly delays amyloid deposition in transgenic mice expressing familial AD (FAD) mutations (FAD-Tg), 5xFAD-Tg mice, which exhibit amyloid deposition by age 2 months, were crossed with apoE-targeted replacement mice to produce the new EFAD-Tg mice. Compared with 5xFAD mice, Aβ deposition was delayed by ∼4 months in the EFAD mice, allowing detection of early changes in Aβ accumulation from 2-6 months. Although plaque deposition is generally greater in E4FAD mice, E2/E3FAD mice have significantly more diffuse and E4FAD more compact plaques. As a first report in FAD-Tg mice, the APOE genotypes had no effect on intraneuronal Aβ accumulation in EFAD mice. In E4FAD mice, total apoE levels were lower and total Aβ levels higher than in E2FAD and E3FAD mice. Profiles from sequential three-step extractions (TBS, detergent, and formic acid) demonstrated that the lower level of total apoE4 is reflected only in the detergent-soluble fraction, indicating that less apoE4 is lipoprotein-associated, and perhaps less lipidated, compared with apoE2 and apoE3. Soluble Aβ42 and oAβ levels were highest in E4FAD mice, although soluble apoE2, apoE3, and apoE4 levels were comparable, suggesting that the differences in soluble Aβ42 and oAβ result from functional differences among the apoE isoforms. Thus, APOE differentially regulates multiple aspects of Aβ accumulation.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
A new EFAD mouse model (5xFAD crossed with human APOE-targeted replacement mice) delays Aβ deposition by ~4 months versus 5xFAD, creating a 2–6-month window to compare APOE genotypes. APOE4 uniquely increases compact plaques, total/soluble Aβ42, and oligomeric Aβ, while total apoE4 is lower and less lipoprotein-associated, but intraneuronal Aβ is comparable across APOE genotypes.
Key findings
- Aβ deposition was delayed ~4 months in EFAD versus 5xFAD mice; plaque deposition was generally greatest in E4FAD, significant at 4 months in frontal cortex and subiculum and at 6 months in frontal cortex. At 6 months in subiculum, E2FAD and E4FAD plaque levels were both significantly higher than E3FAD.
- Plaque morphology differed by APOE genotype: E2FAD and E3FAD had mostly diffuse plaques (>50%), whereas diffuse plaques were significantly lower in E4FAD (~30% at 6 months); compact plaques were ~20% in E2FAD/E3FAD but 40–50% in E4FAD.
- Intraneuronal Aβ increased with age and varied by brain region but showed no significant APOE genotype-specific differences in frontal cortex, subiculum, or CA3.
- Total apoE4 was lower than apoE2/apoE3, reflected only in the TBSX detergent-soluble fraction, suggesting less apoE4 is lipoprotein-associated. Total Aβ42 was higher in E4FAD; soluble Aβ42 was 2-fold higher in cortex and 3-fold higher in hippocampus, and oligomeric Aβ was ~2-fold higher in cortex and 3-fold higher in hippocampus in E4FAD versus E2FAD/E3FAD. At 6 months, TBS-soluble and FA-extracted Aβ42 in E4FAD were at least 4-fold higher than in E2FAD or E3FAD.
Methods
- EFAD mice were generated by crossing 5xFAD mice carrying five FAD mutations with homozygous human APOE2-, APOE3-, or APOE4-targeted replacement mice; male mice were used at 2, 4, and 6 months.
- Brains were analyzed by immunohistochemistry with MOAB-2 and NeuN, Thioflavin S plaque staining and morphology quantification, unbiased stereology for intraneuronal Aβ, three-step sequential extraction (TBS, TBSX, formic acid), and ELISAs for apoE, Aβ42, and oligomeric Aβ; APP levels were checked by Western blot.
- Data were analyzed by one-way or two-way ANOVA with Tukey’s or Bonferroni’s post hoc tests; p < 0.05 was considered significant.
Limitations
- The paper states that female mice were excluded from this initial study for consistency because apoE isoform-specific interactions with Aβ are known to be influenced by gender.
- The paper notes that the 2–6-month window is still early in the overall process of Aβ accumulation and that drug intervention trials have not yet been performed in EFAD mice.
- Evident from the text: the study is limited to male mice, does not report cognitive/behavioral outcomes, and focuses on correlative biochemical and histological changes rather than establishing causal mechanisms.
Model-written summary. Check it against the paper before relying on it.
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Claims the paper makes
28 of 38 cited sources checked · 19 supported · 0 flagged · accuracy not yet measured
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“transgenic mice expressing five FAD mutations (5xFAD), which exhibit accelerated plaque deposition that is significant by 2 months (11)”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Abstract
What the sources say
- Partly supportedcites [11] Oakley, 2006, Intraneuronal β-amyloid aggregates, neurodegeneration, and neuron loss in transgenic mice with five familial Alzheimer's disease mutations: potential factors in amyloid plaque formation, J. Neurosci. sourceExperimental — accuracy not yet measured
The section “5XFAD mice rapidly accumulate massive Aβ42 levels in brain” reports plaque deposition starting at 2 months in line Tg6799, but not in all 5XFAD lines: deposition began at 4 and 6 months in the other two lines. The claim omits that qualification, and the passage does not report a statistical significance test for plaque deposition at 2 months. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Plaque deposition is increased with APOE4 compared with APOE2 and APOE3 in humans and transgenic mice expressing familial AD (FAD) mutations (FAD-Tg) (2)(3)(4)(5).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Abstract
What the sources say
- Partly supportedcites [2] Kim, 2011, Haploinsufficiency of human APOE reduces amyloid deposition in a mouse model of amyloid-β amyloidosis, J. Neurosci. sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) reports APOE-dependent amyloid deposition in humans and Aβ-depositing mouse models, and specifically greater deposition with APOE4 than APOE3 in the APPPS1-21 mouse model. The Results also confirm greater plaque deposition with APOE4 than APOE3 in those mice. The paper does not report an APOE4-versus-APOE2 plaque-deposition comparison; its E4>E3>E2 ordering concerns a possible effect on Aβ clearance. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites [3] Bales, 2009, Human APOE isoform-dependent effects on brain β-amyloid levels in PDAPP transgenic mice, J. Neurosci. source
- Not checked — no full text of the sourcecites [4] Drzezga, 2009, Effect of APOE genotype on amyloid plaque load and gray matter volume in Alzheimer disease, Neurology source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“However, this human study measured A40”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [63] Christensen, 2010, Accumulation of intraneuronal Aβ correlates with ApoE4 genotype, Acta Neuropathol. source
The Results section reports that the authors stained the same human post-mortem patient cohort with G2-10, an antibody specific to Aβ40 peptides. This supports the claim that the human study measured Aβ40, by immunostaining. (LLM, conf=0.92)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“MOAB-2 demonstrates strong intraneuronal immunoreactivity in 5xFAD and 3xTg mouse brain tissue that precedes extracellular A deposition.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [25] Youmans, 2012, Intraneuronal Aβ detection in 5xFAD mice by a new Aβ-specific antibody, Mol. Neurodegener. source
The Abstract Results report strong intraneuronal MOAB-2 immunoreactivity in both 5xFAD and 3xTg brain tissue. The Results section on intraneuronal Aβ and extracellular plaques describes intraneuronal accumulation before substantial extracellular deposition in both models, explicitly noting that it precedes extracellular deposition in 3xTg mice. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“oA-induced deficits in synaptic plasticity (78) and neuronal viability (79) are enhanced in the presence of APOE4 compared with APOE2 and APOE3.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [79] Manelli, 2007, Aβ42 neurotoxicity in primary co-cultures: effect of apoE isoform and Aβ conformation, Neurobiol. Aging source
The Introduction reports that oligomeric Aβ42-induced neurotoxicity was significantly higher in co-cultures with apoE4 glia than with apoE2 or apoE3 glia. The Discussion likewise describes apoE4 as potentiating oligomeric Aβ42-induced neurotoxicity. The finding concerns neuronal viability in an in vitro co-culture model. (LLM, conf=0.94)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“cholesterol release is reduced in primary glial cultures from apoE-TR mice expressing apoE4 compared with glial cells expressing apoE3 (35,73).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [35] Riddell, 2008, Impact of apolipoprotein E (ApoE) polymorphism on brain ApoE levels, J. Neurosci. source
The Animals section describes primary astrocyte cultures prepared from apoE3 and apoE4 targeted-replacement mice. The Results section reports significantly less cholesterol secreted into the medium by apoE4/4 cultures than by apoE3/3 cultures. Page numbers were not supplied. (LLM, conf=0.94)
- Supportedcites [73] Gong, 2002, Apolipoprotein E (ApoE) isoform-dependent lipid release from astrocytes prepared from human ApoE3 and ApoE4 knock-in mice, J. Biol. Chem. source
The Results report that cultured astrocytes from human apoE3 and apoE4 knock-in mice released cholesterol, with significantly more released by apoE3-expressing cells at days 3 and 5. This supports the cited comparison for primary glial cultures, specifically the astrocyte-rich cultures studied. (LLM, conf=0.93)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“MOAB-2 is an anti-A antibody that does not detect APP (25).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [25] Youmans, 2012, Intraneuronal Aβ detection in 5xFAD mice by a new Aβ-specific antibody, Mol. Neurodegener. source
The Results section on biochemical characterization identifies MOAB-2 as an Aβ antibody and reports that it did not detect an APP-sized band in cell lysates or mouse cortical extracts. The IHC Results also report MOAB-2 staining in Aβ-producing tissue but not in tissue that produced APP without Aβ. (LLM, conf=0.95)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- 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
“Overall, plaque deposition was greatest in E4FAD mice compared with E2FAD and E3FAD mice and was significant at 4 months in the frontal cortex and subiculum and at 6 months in the frontal cortex.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Human APOE Genotype-specific Delay of A Accumulation in 5xFAD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA 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
“In general, across age and brain regions, total apoE4 levels were lower than apoE2 and apoE3 (Fig. 4A).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA 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
“It is interesting to note that at 6 months, the levels of A42 in E2FAD and E4FAD mice were both significantly higher than in E3FAD mice.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes
- It may state two separate claims as one. 34
- Probably not a substantial claim. 18
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Introduction of human APOE to existing FAD-Tg mice significantly delays plaque deposition, although once detected, plaque levels are generally greater with APOE4 than APOE3 (3, 6 -8).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Abstract
What the sources say
- Not checked — no full text of the sourcecites [3] Bales, 2009, Human APOE isoform-dependent effects on brain β-amyloid levels in PDAPP transgenic mice, J. Neurosci. source
- Partly supportedcites [6] Buttini, 2002, Modulation of Alzheimer-like synaptic and cholinergic deficits in transgenic mice by human apolipoprotein E depends on isoform, aging, and overexpression of amyloid β peptides but not on plaque formation, J. Neurosci. sourceExperimental — accuracy not yet measured
In the Results section on plaque formation (page unavailable), plaques were absent at 6–15 months in mice with or without human apoE, while 19–24-month-old hAPP/apoE4 mice had more plaques than hAPP/apoE3 mice. The paper supports the APOE4-versus-APOE3 comparison, but it does not show that introducing human APOE significantly delayed plaque deposition relative to hAPP mice lacking apoE. (LLM, conf=0.88)
- Supportedcites [7] Holtzman, 2000, Apolipoprotein E isoform-dependent amyloid deposition and neuritic degeneration in a mouse model of Alzheimer's disease, Proc. Natl. Acad. Sci. U.S.A. source
The Discussion (page not specified) states that both human apoE3 and apoE4 delay Aβ deposition relative to mouse apoE or no apoE. The Results (page not specified) report significantly greater deposition in apoE4- than apoE3-expressing mice once deposits develop. (LLM, conf=0.92)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“This APOE2induced deposition of diffuse plaques is novel in a mouse model and consistent with the previous work by Dr. C. Kawas and co-workers (54,55) who report that increased diffuse plaques are associated with APOE2 in cognitively normal subjects compared with compact plaques in APOE4 AD patients from the oldest of the old study.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Partly supportedcites [54] Berlau, 2009, APOE ϵ2 is associated with intact cognition but increased Alzheimer pathology in the oldest old, Neurology sourceExperimental — accuracy not yet measured
The Results (page unavailable) report a trend toward more diffuse plaques in oldest-old APOE2 carriers versus APOE3/3 carriers, and greater plaque pathology in non-demented APOE2 carriers. They do not establish increased diffuse plaques specifically in cognitively normal APOE2 subjects or the claimed contrast with compact plaques in APOE4 Alzheimer’s patients. The mouse-model novelty is the citing authors’ own finding, not a claim attributed to this source. (LLM, conf=0.86)
- Not checked — no full text of the sourcecites [55] Berlau, 2007, Dissociation of neuropathologic findings and cognition: case report of an apolipoprotein E ϵ2/ϵ2 genotype, Arch. Neurol. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
“In addition, the MOAB-2-based oA42 ELISA detects oligomeric but not monomeric A42 using synthetic preparations characterized previously by our laboratory (data not shown) (47,48).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > ELISAs
What the sources say
- Not checked — no full text of the sourcecites [47] Dahlgren, 2002, Oligomeric and fibrillar species of amyloid-β peptides differentially affect neuronal viability, J. Biol. Chem. source
- Supportedcites [48] Stine, 2003, In vitro characterization of conditions for amyloid-β peptide oligomerization and fibrillogenesis, J. Biol. Chem. source
The citation follows “synthetic preparations characterized previously,” and the paper characterizes preparations of unaggregated and oligomeric Aβ1-42 (Results, “Detection of Aβ1-42 Fibrils…,” page not available). The citing sentence labels the MOAB-2 ELISA result “data not shown”; it does not attribute that assay result to this source. (LLM, conf=0.88)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Female mice were excluded from this initial study for consistency, as apoE isoform-specific interaction with A are known to be influenced by gender (for review (44)).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > EFAD Mice Development
What the sources say
- Partly supportedcites [44] Tai, 2011, Introducing human APOE into Aβ transgenic mouse models, Int. J. Alzheimers Dis. sourceExperimental — accuracy not yet measured
Sections 2.3 and 2.4 report that apoE isoform-related cognitive effects differ between female and male mice, supporting the general concern about sex differences. Sections 3.3 and 3.5 discuss isoform-specific Aβ pathology but do not establish that the apoE–Aβ interaction itself differs by sex. The paper also does not address the citing study’s decision to exclude female mice. (LLM, conf=0.82)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“bexarotene (an RXR agonist) increases apoE levels”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41783
What the sources say
- Partly supportedcites [76] Cramer, 2012, ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models, Science sourceExperimental — accuracy not yet measured
The apoE-expression passage (indexed under Abstract; page not provided) reports increased apoE expression in bexarotene-treated mice after treatment measured in days. The six-hour passage reports a decrease in Aβ, not an increase in apoE, so the added 'within hours' timing is not supported. (LLM, conf=0.88)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
“A renewed interest in the pathological role of plaques has suggested that oA species accumulate at the periphery of densecored plaques (60,61) and that compact plaques enhance A toxicity indirectly by creating a platform on which toxic oA species can accumulate or stabilize.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [60] Koffie, 2009, Oligomeric amyloid β associates with postsynaptic densities and correlates with excitatory synapse loss near senile plaques, Proc. Natl. Acad. Sci. U.S.A. source
The section “Senile Plaques Contain, and Are Surrounded by, a Halo of Aβ Oligomers” reports oligomeric Aβ in and around dense plaque cores. The Discussion proposes that plaques act as a local reservoir of soluble oligomeric Aβ that is toxic to synapses, supporting the citing sentence’s suggested indirect role for plaques. (LLM, conf=0.91)
- Could not verifycites [61] Spires-Jones, 2011, Monitoring protein aggregation and toxicity in Alzheimer's disease mouse models using in vivo imaging, Methods sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) links plaques to nearby neuronal damage and identifies soluble Aβ as a possible mediator. It does not say that oligomeric Aβ accumulates at the periphery of dense-cored plaques or that compact plaques provide a platform that stabilizes it. Searches for oligomers at plaque edges and for the proposed platform mechanism found no passage addressing those points. (LLM, conf=0.70)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. 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
“significantly reduces insoluble A after 3 days”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41783
What the sources say
- Supportedcites [76] Cramer, 2012, ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models, Science source
The passage on acute treatment (section labeled Abstract; page unavailable) reports that insoluble Aβ levels in six-month-old APP/PS1 mice fell by 40% after 72 hours of bexarotene treatment. That supports the claimed reduction after three days, although the passage does not explicitly call the 72-hour result statistically significant. (LLM, conf=0.89)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“These data are in apparent contrast with data from a single study in humans that reports an increase in intraneuronal A with one or two alleles of APOE4 (63).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [63] Christensen, 2010, Accumulation of intraneuronal Aβ correlates with ApoE4 genotype, Acta Neuropathol. source
The Introduction states that this human study found a significant correlation between intraneuronal Aβ accumulation and the presence of at least one ApoE4 allele. The Results likewise report increased intraneuronal Aβ staining in ApoE4 carriers; the claim describes an association, not a causal effect. (LLM, conf=0.92)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“soluble oligomers correlate with cognitive decline (Mini Mental State Examination (MMSE) scores) and tangle stage (20).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [20] Tomic, 2009, Soluble fibrillar oligomer levels are elevated in Alzheimer's disease brain and correlate with cognitive dysfunction, Neurobiol. Dis. source
The Results section reports significant correlations between soluble fibrillar oligomer levels and MMSE scores in several brain regions, as well as significant correlations with tangle stage in all regions examined except the olfactory bulb. The Discussion describes the MMSE relationship as an inverse correlation, consistent with greater cognitive decline at higher oligomer levels. (LLM, conf=0.94)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
“APOE4 carriers can exhibit a differential response to certain therapeutic interventions, complicating the interpretation of drug trials”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41783
What the sources say
- Supportedcites [53] Verghese, 2011, Apolipoprotein E in Alzheimer's disease and other neurological disorders, Lancet Neurol. source
The “Effects of APOE genotype on AD therapeutic response” section reports differences in efficacy or adverse effects between APOE ε4 carriers and non-carriers for some treatments, while noting that other trials found no genotype effect. It concludes that genotype-related differences in efficacy and outcome are important to consider in trial design, supporting the claim’s qualified wording. Page numbers were not provided in our copy. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“decreases soluble A in mice within hours”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41783
What the sources say
- Supportedcites [76] Cramer, 2012, ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models, Science source
The passage describing hippocampal microdialysis in 2-month-old APP/PS1 mice reports that bexarotene lowered interstitial-fluid Aβ40 and Aβ42 within 6 hours. This directly supports the claim about soluble Aβ decreasing in mice within hours. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In FAD-Tg mice, soluble oA suppresses synaptic function”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Partly supportedcites [52] Larson, 2012, Soluble Aβ oligomer production and toxicity, J. Neurochem. sourceExperimental — accuracy not yet measured
In ‘II. Toxicity of Oligomeric Aβ Assemblies’ (page unavailable), the review reports that soluble Aβ oligomers inhibit LTP, a measure of synaptic plasticity. It also describes Aβ-induced neuronal and cognitive deficits in APP-transgenic mice, but does not clearly establish that soluble oligomers suppress synaptic function specifically in those mice. (LLM, conf=0.80)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
“impairs learning and memory (52).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [52] Larson, 2012, Soluble Aβ oligomer production and toxicity, J. Neurochem. source
The Toxicity of Oligomeric Aβ Assemblies section reports that Aβ*56 impairs cognition in Tg2576 mice and is associated with memory decline in other APP-transgenic mouse models of Alzheimer’s disease. It also describes poorer Morris water-maze performance in Tg2576 mice, supporting the claim about learning and memory. (LLM, conf=0.89)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“recent evidence indicates that intraneuronal A accumulation may be an important proximal neurotoxic event in AD pathogenesis (for review see Ref. 56,57).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Supportedcites [56] Gouras, 2010, Intraneuronal β-amyloid accumulation and synapse pathology in Alzheimer's disease, Acta Neuropathol. source
The “Implications of intraneuronal Aβ for Alzheimer’s disease” section says evidence is mounting that intraneuronal Aβ42 is a driving force in Aβ-related AD pathogenesis. The “Pathology” section describes its accumulation in neurites and synapses as leading to their destruction from within. Page numbers were not provided in our copy. (LLM, conf=0.93)
- Supportedcites [57] Bayer, 2010, Intracellular accumulation of amyloid-β: a predictor for synaptic dysfunction and neuron loss in Alzheimer's disease, Front. Aging Neurosci. source
The Introduction describes intraneuronal Aβ accumulation as a hypothesized early pathological event that triggers a cascade leading to neurodegeneration. The Conclusion reports accumulating evidence that intraneuronal Aβ triggers early synaptic deficits and neuron loss, supporting the citing sentence’s qualified claim. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“reduces synaptic plasticity”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
What the sources say
- Partly supportedcites [52] Larson, 2012, Soluble Aβ oligomer production and toxicity, J. Neurochem. sourceExperimental — accuracy not yet measured
The Toxicity of Oligomeric Aβ Assemblies section (page unavailable) says oligomeric Aβ can impair synaptic plasticity. It also discusses Aβ oligomers and deficits in transgenic mouse models, but the passages do not establish that soluble oligomers reduced synaptic plasticity specifically in those mice; the mouse-model findings described concern cognition or neuronal function. (LLM, conf=0.82)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
“although plaque levels at 3 months remained unchanged (76).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41783
What the sources say
- Supportedcites [76] Cramer, 2012, ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models, Science source
The passage on chronic treatment reports that APP/PS1 mice given bexarotene daily for three months had unchanged amyloid plaque burden. The three months refers to treatment duration, not the mice’s age. (LLM, conf=0.95)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“MOAB-2 was developed in the LaDu laboratory and is a high-affinity antibody specific for A that does not detect APP.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > ELISAs
What the sources say
- Supportedcites [25] Youmans, 2012, Intraneuronal Aβ detection in 5xFAD mice by a new Aβ-specific antibody, Mol. Neurodegener. source
The Background identifies MOAB-2 as an antibody specific for Aβ that does not detect APP. The Results report Aβ detection at low antigen and antibody concentrations and show that MOAB-2 did not recognize APP in the tested cell lysates and mouse brain extracts; these findings support the high-affinity description. (LLM, conf=0.88)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- 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
“In E4FAD mice, oA levels were ϳ2-fold higher in the cortex and 3-fold higher in the hippocampus compared with those in E2FAD and E3FAD mice.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41781
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“As observed for apoE, A42 levels were lowest in the cerebellum, higher in the cortex, and highest in the hippocampus (Fig. 4B, p Ͻ 0.001; note the y axis values change for the cerebellum and cortex versus the hippocampus).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
“A accumulation appeared earlier and was greater in the subiculum compared with the frontal cortex, allowing for regional, as well as temporal, comparisons of the effects of the APOE genotype on the progression of A accumulation.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Human APOE Genotype-specific Delay of A Accumulation in 5xFAD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“Specifically, apoE4 levels are significantly lower than apoE2 and apoE3 in the cerebellum at 4 months, in the cortex at 2, 4, and 6 months, and in the hippocampus at 2 and 4 months of age (for specific comparisons, see Fig. 4A).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“Interestingly, total apoE levels in the EFAD mice were lowest in the cerebellum, significantly higher in the cortex, and highest in the hippocampus (Fig. 4A, dashed lines mean the data are collapsed by genotype and age within a region; p Ͻ 0.001).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
“The majority of the plaques in EFAD mice were either diffuse or compact, and this distribution in plaque morphology did not change with age (Fig. 2E).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
“In addition, apoE levels did not change in response to age, and thus there was no APOE genotype-specific response to increasing A accumulation (Fig. 4B).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“FA-extracted A42 levels increased with age for all APOE genotypes and were significantly higher in E4FAD mice at 4 and 6 months compared with E2FAD and E3FAD mice (Fig. 5B).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“The reverse pattern was observed with compact plaques; ϳ20% of the plaques in E2FAD and E3FAD mice were compact, whereas 40 -50% of plaques in E4FAD mice were compact.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“In the cortex, A42 levels were generally low at 2 months but increased significantly by 4 months such that E4FAD Ͼ E3FAD ϭ E2FAD.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“In the hippocampus, A42 levels were low at 2 months but increased significantly by 4 and 6 months such that E4FAD Ͼ E3FAD ϭ E2FAD.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“ApoE2 and apoE3 were extracted primarily to the TBSX fraction, whereas apoE4 levels were significantly lower in this fraction at 2, 4, and 6 months.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“Soluble apoE levels were comparable in the cortex (Fig. 6A) and hippocampus (Fig. 6B) and did not vary significantly by APOE genotype.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“Compared with 5xFAD mice, A deposition was delayed ϳ4 months in the EFAD mice, with accumulation earliest in E4FAD Ͼ E3FAD ϭ E2FAD.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Human APOE Genotype-specific Delay of A Accumulation in 5xFAD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“In E2FAD and E3FAD mice the majority of plaques were diffuse, accounting for more than 50% of total plaques, whereas diffuse plaques were significantly lower in E4FAD mice (e.g.30% at 6 months).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“In addition, from 4 to 6 months, the proportion of diffuse plaques decreased and that of compact plaques increased only in the E4FAD mice (Fig. 2E).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > APOE4-specific Changes in A Accumulation in AD Tg Mice
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“Further, in both the cortex and the hippocampus, soluble A42 levels were 2-fold and 3-fold higher, respectively, in E4FAD mice compared with E2FAD and E3FAD mice.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41781
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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, analysis of plaque morphology revealed that whereas the majority of the APOE4 plaques are compact, the majority of the APOE2 plaques are diffuse.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“whereas the EFAD mice express almost exclusively A42”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
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
“Further, this apoE4-specific distribution appears to occur in the hippocampus and cortex, which are AD-susceptible brain regions, and not the cerebellum, a disease-resistant region.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“Compared with 5xFAD mice, A deposition was delayed by ϳ4 months in the EFAD mice, allowing detection of early changes in A accumulation from 2-6 months.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41783
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“In EFAD mice, A deposition is delayed ϳ4 months compared with 5xFAD mice, creating a window from 2 to 6 months during which comparisons of multiple forms of A accumulation can be measured, although this is still early in the overall process of A accumulation in either the hippocampus or the cortex.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“For example, crossing apoE-targeted replacement mice (apoE-TR) (9) with PDAPP mice (10) delays plaque deposition from ϳ10 to 18 months, although once detected, plaque levels are greater with APOE4 than APOE3 (3).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Abstract
What the sources say
- Not checked — no full text of the sourcecites [3] Bales, 2009, Human APOE isoform-dependent effects on brain β-amyloid levels in PDAPP transgenic mice, J. Neurosci. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“The primary genetic risk factor for Alzheimer disease (AD) 4 is APOE4, increasing the risk by ϳ4and 15-fold with a single or double allele, whereas APOE2 reduces the risk compared with APOE3.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Abstract
What the sources say
- Not checked — no full text of the sourcecites [4] Drzezga, 2009, Effect of APOE genotype on amyloid plaque load and gray matter volume in Alzheimer disease, Neurology source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. 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
“Overall, these data demonstrate that APOE genotype modulates A speciation, an effect likely mediated by functional differences among the apoE isoforms.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 41781
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
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
“The number of neurons containing intraneuronal A was determined using unbiased stereology (51) and counted by an investigator blinded to APOE genotype using sections immunostained with MOAB-2 (for A) and NeuN.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Intraneuronal A Counts
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“This ELISA pairing detects synthetic oA preparations but not monomeric A using preparations of oA optimized for the original protocol (data not shown) (46).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > ELISAs
What the sources say
- Not checked — no full text of the sourcecites [46] Moore, 2009, Biophysical analyses of synthetic amyloid-β(1–42) aggregates before and after covalent cross-linking. Implications for deducing the structure of endogenous amyloid-β oligomers, Biochemistry source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“which is one possible explanation for the discrepancy.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
“Thio-S plaque staining and quantification was conducted by an investigator blinded to the APOE genotype using every ninth tissue section for six consecutive sections, beginning with the lateral-most section in the region of interest (ROI).”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Thioflavin S Staining for Plaques
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“The number of neurons containing intraneuronal A was determined using unbiased stereology (51) and counted by an investigator blinded to APOE genotype using sections immunostained with MOAB-2 (for A) and NeuN.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > Intraneuronal A Counts
What the sources say
- Not checked — no full text of the sourcecites [51] West, 1991, Unbiased stereological estimation of the total number of neurons in thesubdivisions of the rat hippocampus using the optical fractionator, Anat. Rec. source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably 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
“This effect would be enhanced with APOE4, as it is associated with a larger proportion of compact plaques.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > DISCUSSION
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
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 follow the University of Illinois at Chicago Institutional Animal Care and Use Committee protocols.”
§ APOE4-specific Changes in A Accumulation in a New Transgenic Mouse Model of Alzheimer Disease * □ S > EFAD Mice Development
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper relies on this without support.
Human apoE in apoE-TR mice is expressed primarily by glia at physiologically regulated levels.
“ApoE-TR mice are perhaps the most biologically relevant transgenic mouse model for apoE, as human apoE is expressed primarily by glia at physiologically regulated levels.”
The paper relies on this without support.
APOE4 is the greatest risk factor for Alzheimer disease.
“APOE4 is the greatest risk factor for Alzheimer disease (AD)”
The paper relies on this without support.
It is unclear how the APOE genotype affects plaque morphology, intraneuronal Aβ, soluble Aβ42, and oligomeric Aβ (oAβ), particularly in vivo.
“However, it remains unclear how the APOE genotype affects plaque morphology, intraneuronal A, soluble A42, and oligomeric A (oA), particularly in vivo.”
The paper relies on this without support.
No studies have yet reported the effect of APOE genotype on intraneuronal Aβ accumulation in an apoE/FAD-Tg mouse.
“To our knowledge, no studies have yet reported the effect of APOE genotype on intraneuronal A accumulation in an apoE/ FAD-Tg mouse.”
The paper relies on this without support.
Introduction of human APOE significantly delays amyloid deposition in transgenic mice expressing familial AD (FAD) mutations.
“As the introduction of human APOE significantly delays amyloid deposition in transgenic mice expressing familial AD (FAD) mutations (FAD-Tg)”
The paper relies on this without support.
Intraneuronal Aβ has been correlated with cognitive deficits in FAD-Tg mice.
“Indeed, intraneuronal A has been correlated with cognitive deficits in FAD-Tg mice.”
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 cited source doesn’t support the claim as written.
In the citing paper
“We previously demonstrated that RXR agonists induce an increase in ABCA1 expression with an increase in apoE4 lipidation and a decrease in both total Aβ42 and soluble Aβ in EFAD (5xFAD+/-/APOE4+/+)-Tg mice [13].”
From Inhibition of ACAT as a Therapeutic Target for Alzheimer's Disease Is Independent of ApoE4 Lipidation (2023) · cites this paper as [13]
Checked by a reasoning model — may be wrong.
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
“The APOE4 allele is a major genetic risk factor for late-onset AD and was previously shown to accelerate AD progression in humans and in mouse models 6-11 .”
From APOE4 impairs the microglial response in Alzheimer’s disease by inducing TGFβ-mediated checkpoints (2023) · 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
“These results bear a striking resemblance to those from the Aβ plaque-depositing mice120,128 and indicate that the effect of APOE4 in AD is due not only to the increased propensity of proteins to aggregate in the presence of APOE4, but also to the way APOE4 modulates the brain response to those aggregates once formed.”
From Multifaceted roles of APOE in Alzheimer disease (2024) · cites this paper as [120]
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
“Extracellularly, ApoE4 aggregates promote A oligomerization (Youmans et al., 2012;Tai et al., 2013).”
From ApoE4 Alters ABCA1 Membrane Trafficking in Astrocytes (2019) · cites this paper as Youmans et al., 2012
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 addition, ApoE4 AD mouse models have a greater percentage of lipid-poor and aggregated ApoE than their ApoE3 counterparts (Youmans et al., 2012).”
From ApoE4 Alters ABCA1 Membrane Trafficking in Astrocytes (2019) · cites this paper as Youmans et al., 2012
Experimental — accuracy not yet measured
The cited source says what the claim attributes to it.
In the citing paper
“Previous studies support this, with E4FAD (APOE4+5xFAD) mice showing increased amyloid deposition, specifically more compact plaques, compared to E3FAD (APOE3+5xFAD) mice (Youmans et al., 2012).”
From Plcg2M28L Interacts With High Fat/High Sugar Diet to Accelerate Alzheimer’s Disease-Relevant Phenotypes in Mice (2022) · cites this paper as Youmans et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“The APOE4 allele is the strongest genetic risk factor for late-onset Alzheimer's disease (AD).”
From APOE4 impairs the microglial response in Alzheimer’s disease by inducing TGFβ-mediated checkpoints (2023) · cites this paper as [10]
The cited source says what the claim attributes to it.
In the citing paper
“Nevertheless other studies have also reported that APOE2 expression is associated with similar or even higher plaque load than APOE3 (Rodriguez et al, 2014; Youmans et al, 2012; Bales et al, 2009; Dodart et al, 2005).”
From APOE from astrocytes restores Alzheimer’s Aβ-pathology and DAM-like responses in APOE deficient microglia (2024) · cites this paper as Youmans et al, 2012
The cited source says what the claim attributes to it.
In the citing paper
“Although expressed at comparable levels, apoE4 levels in brain are lower than apoE3 levels in both humans and Tg mouse models [13–15], suggesting that apoE4 is unstable and undergoes accelerated degradation, likely due to the observed reduced lipidation state of apoE4-lipoproteins compared to apoE3-lipoproteins [16–23].”
From Inhibition of ACAT as a Therapeutic Target for Alzheimer's Disease Is Independent of ApoE4 Lipidation (2023) · cites this paper as [13]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“verified that plaque deposition requires BACE1 activity, as previously shown [17-20].”
From Neuron loss in the 5XFAD mouse model of Alzheimer’s disease correlates with intraneuronal Aβ42 accumulation and Caspase-3 activation (2013) · cites this paper as [19]
Experimental — accuracy not yet measuredIn the citing paper
“This is further complicated by the fact that expression of different isoforms of human ApoE in transgenic mice results in different levels of plaque and CAA burden with apoE4 expression enhancing amyloid deposition compared to apoE3 or apoE2 [3, 21, 40, 59, 86, 178].”
From Alzheimer's disease: experimental models and reality (2017) · cites this paper as [178]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Self-check results appear here once an independent check has confirmed them.
Cited works that were retracted
Works this paper cites that were later retracted, from the retraction notices publishers deposit. Major when the notice came out before this paper was published.
Cites a retracted work: 10.1523/jneurosci.6637-10.2011
InfoThe cited work was retracted on 2015-02-25 (notice 10.1523/jneurosci.5236-14.2015), not before this paper was published (2012-12).
Cited work 10.1523/jneurosci.6637-10.2011 · retracted 2015-02-25 · notice 10.1523/jneurosci.5236-14.2015 · this paper published 2012-12
“Winton, 2011, Intraneuronal APP, not free Aβ peptides in 3xTg-AD mice: implications for Tau versus Aβ-mediated Alzheimer neurodegeneration, J. Neurosci., 31, 7691, 10.1523/JNEUROSCI.6637-10.2011”
Citations
Cites
1 retracted
Winton, M. J., Lee, E. B., Sun, E., Wong, M. M., Leight, S., Zhang, B., Trojanowski, J., & Lee, V. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6637-10.2011 · Cited by 110
RetractedAmyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid β-peptide
Haass, C., & Selkoe, D. J. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2101 · Cited by 4,744 · cited 1×
“By IHC, intraneuronal A (12–14) and perhaps specific plaque morphologies (15, 16) are thought to contribute to A pathology, although amyloid plaque burden per semay not be neurotoxic (17).”
BackgroundOakley, H., Cole, S. L., Logan, S., Maus, E., Shao, P., Craft, J., Guillozet-Bongaarts, A., Ohno, M., Disterhoft, J., Van Eldik, L., et al. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1202-06.2006 · Cited by 3,530 · cited 5×
“Given the abundant A pathology in 5xFAD mice at 2 months (11), total A deposition was examined in 2-, 4-, and 6-month-old EFADmice by IHCusing themonoclonal anti-A antibody MOA -2 (Fig.”
BackgroundMethodInfluentialWest, M. J., Slomianka, L., & Gundersen, H. J. G. (1991) · The Anatomical Record · doi:10.1002/ar.1092310411 · Cited by 2,994 · cited 1×
“The number of neurons containing intraneuronal A was determined using unbiased stereology (51) and counted by an investigator blinded to APOE genotype using sections immunostained with MOAB-2 (for A ) and NeuN.”
MethodAlzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein
Games, D., Adams, D., Alessandrini, R., Barbour, R., Borthelette, P., Blackwell, C., Carr, T., Clemens, J., Donaldson, T., Gillespie, F., et al. (1995) · Nature · doi:10.1038/373523a0 · Cited by 2,516 · cited 1×
“For example, crossing apoE-targeted replacement mice (apoE-TR) (9) with PDAPP mice (10) delays plaque deposition from 10 to 18 months, although once detected, plaque levels are greater with APOE4 than APOE3 (3).”
BackgroundAlzheimer Mechanisms and Therapeutic Strategies
Huang, Y., & Mucke, L. (2012) · Cell · doi:10.1016/j.cell.2012.02.040 · Cited by 1,758
The Alzheimer's Disease Neuroimaging Initiative
Mueller, S. G., Weiner, M. W., Thal, L. J., Petersen, R. C., Jack, C., Jagust, W., Trojanowski, J. Q., Toga, A. W., & Beckett, L. (2005) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2005.09.008 · Cited by 1,525
Oligomeric and fibrillar species of amyloid-β peptides differentially affect neuronal viability
Dahlgren, K. N., Manelli, A. M., Stine, W. B., Baker, L. K., Krafft, G. A., & LaDu, M. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201750200 · Cited by 1,452 · cited 1×
“In addition, the MOAB-2-based oA 42 ELISA detects oligomeric but not monomeric A 42 using synthetic preparations characterized previously by our laboratory (data not shown) (47, 48).”
MethodHuman ApoE isoforms differentially regulate brain amyloid-β peptide clearance
Castellano, J. M., Kim, J., Stewart, F. R., Jiang, H., DeMattos, R. B., Patterson, B. W., Fagan, A. M., Morris, J. C., Mawuenyega, K. G., Cruchaga, C., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002156 · Cited by 1,242
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Apolipoprotein E loss of function: Influence on murine brain markers of physiology and pathology
Buchanan, H. M., Hull, C. E., Barraza, M. C., Delibegović, M., & Platt, B. (2022) · Aging Brain · doi:10.1016/j.nbas.2022.100055 · Cited by 7
Mouse models of Anti-Aβ immunotherapies
Pikus, P., Turner, R. S., & Rebeck, G. W. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00836-x · Cited by 6
“Similar to the 1.5 months [11] 4 months [12] Very Low [13] Low [12] Some CAA in E4FAD [15] at 8–10 months [12] GFP-microglia, APOE2/3/4 [15] APOE4 [12] Jackson Laboratory Stock #034840 Jackson Laboratory Stock #034848 Tg2576 11–13 months [17] High [18] By 19 months most pial arteries are affected…”
InfluentialSelf-citationObesity affects brain cortex gene expression in an APOE genotype and sex dependent manner
Pandit, H., Jones, N. S., & Rebeck, G. W. (2024) · International Journal of Obesity · doi:10.1038/s41366-024-01481-y · Cited by 6
Self-citationAguilar-Pineda, J. A., Paco-Coralla, S. G., Febres-Molina, C., Gamero-Begazo, P. L., Shrivastava, P., Vera-López, K. J., Dávila-Del-Carpio, G., López-Casaperalta, P., Gómez, B., & Cardenas, C. L. L. (2022) · Biomolecules · doi:10.3390/biom12040499 · Cited by 7
“There are several studies in this regard and, in particular, some suggest increasing ApoE4 lipidation to reduce the intraneuronal accumulation of Aβ and thus alleviate cognitive impairment in ApoE4 targeted replacement (TR) mice [23,24].”
BackgroundAdvances in the Study of APOE and Innate Immunity in Alzheimer’s Disease
Li, Y., Chang, J., Chen, X., Liu, J., & Zhao, L. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230179 · Cited by 6
Takebayashi, Y., Yamazaki, Y., Yamada, H., Yazawa, K., Nakamori, M., Kurashige, T., Morino, H., Takahashi, T., Sotomaru, Y., & Maruyama, H. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.10.038 · Cited by 6
Balu, D., Valencia‐Olvera, A. C., Deshpande, A., Narayanam, S., Konasani, S., Pattisapu, S., York, J. M., Thatcher, G. R. J., LaDu, M. J., & Tai, L. M. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1374825 · Cited by 6
Self-citationSawmiller, D. R., Koyama, N., Fujiwara, M., Segawa, T., Maeda, M., & Mori, T. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104846 · Cited by 5
“Consistent with the other reports from human AD cases (4) and AD mouse models (49, 50), we show that vehicle-treated APP/PS1/E4 mice demonstrate significant and isoformspecific deterioration of cerebral amyloid pathology versus vehicle-treated APP/PS1/E2 or APP/PS1/E3 mice (see Figs.”
ResultZhou, H., Yao, W., Shan, Q., Zhang, X., Zhang, D., Che, J., & Bai, F. (2024) · Materials & Design · doi:10.1016/j.matdes.2024.113322 · Cited by 5
Apolipoprotein E4 inhibits γ‐secretase activity via binding to the γ‐secretase complex
Sun, Y., Islam, S., Gao, Y., Nakamura, T., Zou, K., & Michikawa, M. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15750 · Cited by 5
van Kruining, D., Losen, M. H., Dehairs, J., Swinnen, J. V., Waelkens, E., Honing, M., & Martínez‐Martínez, P. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.106923 · Cited by 5
“In short, human APOE3 or APOE4 knock-in mice in which the mouse APOE gene was replaced by human APOE were crossbred with 5xFAD mice (Jackson Laboratory) carrying human familial AD mutations PSEN1 and APP to obtain E3FAD and E4FAD mice (Youmans et al., 2012; Oakley et al., 2006).”
McGill, C. J., Christensen, A., Qian, W., Thorwald, M. A., Godoy-Lugo, J. A., Namvari, S., White, O. S., Finch, C. E., Benayoun, B. A., & Pike, C. J. (2025) · Communications Medicine · doi:10.1038/s43856-025-00942-3 · Cited by 4
Borchelt, D. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120414 · Cited by 3
Higher Neuronal Facilitation and Potentiation with APOE4 Suppressed by Angiotensin II
Scheinman, S. B., Tseng, K. Y., Alford, S. T., & Tai, L. M. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03556-9 · Cited by 3
“EFAD mice were produced by crossing either APOE3 - or APOE4 -targeted replacement mice with mice that express 5 familial Alzheimer’s disease (5xFAD) mutations (APP K670N/M671L + I716 V + V717I and PS1 M146L + L286 V) [46].”
Self-citationHe, M., Lian, T., Guo, P. F., Zhang, W., Zhang, Y., Huang, Y. M., Liu, G., Guan, H., Li, J., Luo, D., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14440 · Cited by 2
Comparison of the ApoE allelic variants in the formation of intracerebral Aβ deposits
Xu, G. M., Angelle, C., Huilgol, D., Sacilotto, P., McFarland, K. N., Fromholt, S., Lopez, A., Vo, Q., Rivasplata, A., Brkic, S., et al. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107105 · Cited by 2
Fagla, B. M., York, J. M., Christensen, A., Rosa, C. D., Balu, D., Pike, C. J., Tai, L. M., & Buhimschi, I. A. (2024) · Scientific Reports · doi:10.1038/s41598-024-66489-w · Cited by 2
“This transgenic mouse model was originally developed by Dr. Mary Jo LaDu as previously described 12 .”
MethodSelf-citationden Hoedt, S., Crivelli, S. M., Dorst‐Lagerwerf, K. Y., Leijten, F. P. J., Losen, M. H., de Vries, H. E., Sijbrands, E. J. G., Verhoeven, A. J. M., Martínez‐Martínez, P., & Mulder, M. T. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16176 · Cited by 2
The Effect of FTY720 on Sphingolipid Imbalance and Cognitive Decline in Aged EFAD Mice
Luo, Q., Crivelli, S. M., Zong, S., Giovagnoni, C., van Kruining, D., Mané-Damas, M., den Hoedt, S., Berkeš, D., de Vries, H. E., Mulder, M. T., et al. (2024) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-230053 · Cited by 3
Türk Popülasyonunda APOE Polimorfizmleri ve Alzheimer Hastalığı Arasındaki İlişki
Çilingir, O., Adapınar, B. D. Ö., Aras, B. D., Gökalp, E. E., Özkan, S., Arslan, S., Haziyeva, K., Kocagil, S., Bilgin, M., & Artan, S. (2019) · OSMANGAZİ JOURNAL OF MEDICINE · doi:10.20515/otd.553900 · Cited by 2
Evaluation of B0-correction of relative CBF maps using tagging distance dependent Z-spectrum (TADDZ)
Damen, F. C., Tain, R., Thomas, R., Li, W., Tai, L. M., & Cai, K. (2019) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2019.10.002 · Cited by 2
Self-citationStephen, T., Breningstall, B. M., Suresh, S., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-2002470/v1 · Cited by 2
McGill, C. J., Christensen, A., Qian, W., Thorwald, M. A., Lugo, J. G., Namvari, S., White, O. S., Finch, C. E., Benayoun, B. A., & Pike, C. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.12.584678 · Cited by 2
“To determine if the longevity-promoting intervention 17αE2 provides greater protection against systemic aging phenotypes in the context of the APOE4 allele, we used strains of mice with humanized APOE3 or APOE4 sequences [28].”
BackgroundMethodKaloss, A. M., Browning, J. L., Li, J., Pan, Y., Watsen, S., Sontheimer, H. W., Theus, M. H., & Olsen, M. L. (2025) · Alzheimer s Research & Therapy · doi:10.1186/s13195-025-01876-7 · Cited by 1
Tau Phosphorylation and Amyloid-β Deposition in the Presence of Formaldehyde
Lü, J., & He, R. (2017) · Springer eBooks · doi:10.1007/978-94-024-1177-5_9 · Cited by 1
Revisiting the genetics of APOE
Carmona, S., Kun‐Rodrigues, C., Brás, J., & Guerreiro, R. J. (2017) · UCL Discovery (University College London) · Cited by 1
Johnson, N. R., Wang, A. C.-J., Coughlan, C. M., Sillau, S., Lucero, E., Viltz, L., Markham, N. E., Allen, C., Dhanasekaran, A. R., Chial, H. J., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.28.437389 · Cited by 1
Rodriguez, G. A. (2014) · DigitalGeorgetown (Georgetown University Library)
Alzheimer’s Disease Therapeutics Targeting Apolipoprotein E
Liao, F., & Holtzman, D. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802173-6.00010-1
Carter, A. B. (2017) · D-Scholarship@Pitt (University of Pittsburgh)
AXL receptor tyrosine kinase regulates Apolipoprotein E expression
Zhao, W. (2019) · cIRcle (University of British Columbia) · doi:10.14288/1.0372324
The APOE4 Mouse as a Model of Chemotherapy-induced Cognitive Impairments and Senescence
Demby, T. C. (2021) · DigitalGeorgetown (Georgetown University Library)
Victoroff, J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139696432.002
Exploring sphingolipid function in the pathogenesis of Alzheimer’s disease
Luo, Q. (2022) · Research Publications (Maastricht University) · doi:10.26481/dis.20220215ql
Essers, E., Binter, A.-C., Neumann, A., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4102813
Induced-pluripotent stem cells and neuroproteomics as tools for studying neurodegeneration
Brandão‐Teles, C., Zuccoli, G. S., Vrechi, T. A. D. M., Ramos-da-Silva, L., Santos, A. V. S., Crunfli, F., & Martins‐de‐Souza, D. (2024) · Biochemical Society Transactions · doi:10.1042/bst20230341
APOE2 Heterozygosity Reduces Hippocampal Soluble Amyloid-β42 Levels in Non-Hyperlipidemic Mice
Valencia‐Olvera, A. C., Balu, D., Moore, A., Shah, M., Ainis, R., Xiang, B., Saleh, Y., Cai, D., LaDu, M. J., & Tai, L. M. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231210
Self-citationAmyloid, Tau, and ApoE: Revisiting Hypotheses of Alzheimer's Disease
Yao, B., Kuang, M., Jiang, D. F., & Xu, C. (2025) · Theoretical and Natural Science · doi:10.54254/2753-8818/2024.19396
Baowan, 李. L., Mian, 谢. X., Wenhao, 刘. L., Weisong, 赵. Z., Haoyu, 李. L., & Changliang, 郭. G. (2025) · Laser & Optoelectronics Progress · doi:10.3788/lop251328
The Christchurch point mutation in mouse APOE reduces Aβ-induced tau and α-synuclein pathologiesPreprint
Soto-Faguás, C. M., O’Niel, A., Mueller, P. A., Sanchez-Molina, P., Woltjer, R. L., Raber, J., & Unni, V. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.05.686857
“Given that human APOE KI into the mouse locus delays Aβ pathology formation on its own 29 and to avoid potential confounds associated with altered interactions between human APOE with different murine receptors, we decided to generate the murine APOE R128S CC allele by using CRISPR/Cas9 technology…”
He, K., Zhang, Z., Li, Y., Xiong, W., Xing, Y., Gao, W., Kong, W., Chen, L., Yang, X., & Dai, Z. (2025) · CNS Neuroscience & Therapeutics · doi:10.1002/cns.70694
Johnson, N. R., Wang, A. C.-J., Coughlan, C. M., Sillau, S., Lucero, E., Viltz, L., Markham, N. E., Allen, C., Dhanasekaran, A. R., Chial, H. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20193570
Ringland, C., Schweig, J. E., Eisenbaum, M., Paris, D., Ait‐Ghezala, G., Mullan, M., Crawford, F., Abdullah, L. I., & Bachmeier, C. (2021) · Figshare · doi:10.6084/m9.figshare.14677003
Sepulveda, J., Kim, J. Y., Binder, J., Vicini, S., & Rebeck, G. W. (2024) · Figshare · doi:10.6084/m9.figshare.26691931
Self-citationSepulveda, J., Kim, J. Y., Binder, J., Vicini, S., & Rebeck, G. W. (2024) · Figshare · doi:10.6084/m9.figshare.26691937
Self-citationJohnson, N. R., Wang, A. C.-J., Coughlan, C. M., Sillau, S., Lucero, E., Viltz, L., Markham, N. E., Allen, C., Dhanasekaran, A. R., Chial, H. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20193564
Valencia‐Olvera, A. C., Balu, D., Bellur, S., McNally, T. P., Saleh, Y., Pham, D., Ghura, S., York, J. M., Johansson, J. O., LaDu, M. J., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24844648
Self-citationValencia‐Olvera, A. C., Balu, D., Bellur, S., McNally, T. P., Saleh, Y., Pham, D., Ghura, S., York, J. M., Johansson, J. O., LaDu, M. J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.24844709
Self-citationValencia‐Olvera, A. C., Balu, D., Bellur, S., McNally, T. P., Saleh, Y., Pham, D., Ghura, S., York, J. M., Johansson, J. O., LaDu, M. J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26654539
Self-citationJohnson, N. R., Wang, A. C.-J., Coughlan, C. M., Sillau, S., Lucero, E., Viltz, L., Markham, N. E., Allen, C., Dhanasekaran, A. R., Chial, H. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20193558
Valencia‐Olvera, A. C., Balu, D., Bellur, S., McNally, T. P., Saleh, Y., Pham, D., Ghura, S., York, J. M., Johansson, J. O., LaDu, M. J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26654542
Self-citationValencia‐Olvera, A. C., Balu, D., Bellur, S., McNally, T. P., Saleh, Y., Pham, D., Ghura, S., York, J. M., Johansson, J. O., LaDu, M. J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26654536
Self-citationSepulveda, J., Kim, J. Y., Binder, J., Vicini, S., & Rebeck, G. W. (2024) · Figshare · doi:10.6084/m9.figshare.26691934
Self-citationMouse models elucidating the role of apolipoprotein E in neurological conditions
Torres, E. R. S., & Raber, J. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-29090-9.00001-5
Role of apolipoprotein E4 in alzheimer’s disease pathogenesis and emerging therapeutic strategies
Natarajan, S., & Saraswathy, S. D. (2025) · Metabolic Brain Disease · doi:10.1007/s11011-025-01761-0
“In amyloidogenic contexts (e.g., APP/PS1), APOE4-TR animals demonstrate expedited amyloid-beta accumulation, diminished Aβ clearance, and an earlier onset of cogni - tive deterioration relative to APOE3-TR and APOE2-TR counterparts (Youmans et al. 2012 ).”
Investigating gender differences in Alzheimer's disease
Fouad, G. I., Ando, H., & Ichihara, G. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877251410204 · Cited by 2
Pikus, P., Healey, G. S., Xia, E., Shautidze, G., Siddapureddy, N., Lee, Y., Albanese, C., Rodriguez, O. C., Turner, R. S., & Rebeck, G. W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.09.704876
Self-citationZhang, X., Zhuang, D., Lai, C., Zheng, C., Soh, Z. D., Wagner, S. K., Cai, V. Y., Yang, Z., Wang, S., Geng, X., et al. (2026) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2026.101504
17α-Estradiol Confers Limited Protection Against APOE4 Phenotypes in Middle-Aged Female MicePreprint
McGill, C. J., Christensen, A., Namvari, S., Thorwald, M. A., Anson, H., Vermulst, M., Finch, C. E., Benayoun, B. A., & Pike, C. J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.06.743074
“The mice were generated from a breeding colony of EFAD ( APOE +/+ , 5xFAD +/- ) mice [28] but were non-carriers of the 5xFAD Alzheimer’s-related genes ( APOE +/+ , 5xFAD -/- ).”
Metadata
- Authors
- Youmans, K. L., Tai, L. M., Nwabuisi-Heath, E., Jungbauer, L., Kanekiyo, T., Gan, M., Kim, J., Eimer, W. A., Estus, S., Rebeck, G. W., Weeber, E. J., Bu, G., Yu, C., & LaDu, M. J.
- Affiliations
- University of Illinois Chicago (US)
- Mayo Clinic in Florida (US)
- Washington University in St. Louis (US)
- Northwestern University (US)
- University of Kentucky (US)
- Georgetown University (US)
- University of South Florida (US)
- Corresponding author
- LaDu, Mary Jo
- ORCID
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2012-12
- Volume
- 287
- Issue
- 50
- Pages
- 41774-41786
- ISSN
- 0021-9258 (ISSN-L)
- PMC
- PMC3516726
- OpenAlex
- W2168481427
- Semantic Scholar
- 4a4316d49bb3198e00a5f0da10f93ed86c113688
- Cited by
- 268
- References
- 93
- Citations by year
- 2026: 7 · 2025: 18 · 2024: 28 · 2023: 21 · 2022: 25 · 2021: 23 · 2020: 25 · 2019: 23 · 2018: 16 · 2017: 18 · 2016: 19 · 2015: 18 · 2014: 15 · 2013: 12
- FWCI
- 4.86
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Figshare (submittedVersion)
- Rare & Special e-Zone (The Hong Kong University of Science and Technology) (submittedVersion)
- Funders
- Alzheimer's Association (P01AG030128-03S1, ZEN-08-899000, UL1RR029879)
- National Institutes of Health
- University of Illinois at Urbana-Champaign
- National Institute on Aging (P01AG030128, R01AG027924, R01AG035379, R01AG035355, T32AG036697)
- National Institute of Neurological Disorders and Stroke (P01NS074969)
- National Center for Research Resources (UL1RR029879)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- APOE ε4, Alzheimer's disease, amyloid-beta deposition, APOE isoforms, 5xFAD mice, amyloid plaques, intraneuronal amyloid-beta, amyloid-beta oligomers, familial Alzheimer's disease
- MeSH terms
- Alzheimer Disease, Animals, Disease Models, Animal, Genotype, Humans, Mice, Transgenic, Mutation, Amyloid beta-Peptides, Protein Isoforms, Mice, Apolipoprotein E4
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