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Sterile inflammation: sensing and reacting to damage
Open accessAbstract
Over the past several decades, much has been revealed about the nature of the host innate immune response to microorganisms, with the identification of pattern recognition receptors (PRRs) and pathogen-associated molecular patterns, which are the conserved microbial motifs sensed by these receptors. It is now apparent that these same PRRs can also be activated by non-microbial signals, many of which are considered as damage-associated molecular patterns. The sterile inflammation that ensues either resolves the initial insult or leads to disease. Here, we review the triggers and receptor pathways that result in sterile inflammation and its impact on human health.
Overview
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TL;DR
Sterile inflammation is triggered when endogenous damage-associated molecular patterns (DAMPs) released by injured or necrotic cells activate the same pattern recognition receptors (PRRs) that sense microbial pathogens, notably TLRs, the NLRP3 and AIM2 inflammasomes, and C-type lectins. The review argues that IL-1 (particularly IL-1α and IL-1β) is a central mediator of these responses and a promising therapeutic target across gout, atherosclerosis, type 2 diabetes and cancer.
Key findings
- DAMPs are endogenous molecules normally sequestered intracellularly (HMGB1, HSPs, ATP, uric acid) or generated by extracellular matrix degradation (hyaluronan, heparan sulphate, biglycan) that become immunostimulatory when released by necrosis; their relative importance and redundancy remain unresolved — uric acid depletion reduced neutrophil recruitment after acetaminophen-induced liver injury in two mouse models but had no effect in particulate-induced inflammation.
- NLRP3 is activated by structurally diverse sterile stimuli (asbestos, silica, MSU and CPPD crystals, cholesterol crystals, β-amyloid fibrils); NLRP3-deficient mice showed decreased inflammation in gout, asbestosis and silicosis models, and LDL-receptor-deficient mice infused with NLRP3-deficient bone marrow had lower IL-1β, smaller atherosclerotic lesions and less neutrophilic infiltration.
- Three proposed mechanisms of NLRP3 activation — ATP/P2RX7, lysosomal damage with cathepsin B, and ROS — are each supported only partially, with contradictory data (e.g., TXNIP-deficient macrophages showed impaired IL-1β in one study but no difference in another; p22phox- or Gp91phox-deficient macrophages had normal caspase 1 activation).
- Therapeutic blockade of IL-1R with anakinra produced significant symptom relief in all ten evaluated gout patients who could not tolerate or respond to prior therapy, and improved glucose and reduced IL-6 and C-reactive protein in a randomized trial of 70 patients with type 2 diabetes; results in osteoarthritis and rheumatoid arthritis were not promising.
Methods
- Narrative review (not a primary study) synthesizing the literature on sterile inflammation, its triggers, receptor pathways and disease implications.
- Evidence drawn from in vitro and in vivo mouse models (including knockout and bone marrow chimera studies) and human clinical trials, organized around three proposed mechanisms: PRR activation by DAMPs, release of intracellular cytokines such as IL-1α, and direct activation via non-PRR receptors such as RAGE.
- No new data, systematic search strategy or meta-analysis is reported.
Limitations
- Stated by the paper: it is unclear whether DAMPs identified by in vitro cytokine induction (HSPs, S100 proteins, ATP) actually drive sterile inflammation in vivo; stimulatory activity of some purified DAMPs may reflect bacterial product contamination (HSPs and HMGB1 bind LPS); many DAMPs interact with several receptors, so the significance of individual interactions is unresolved; the relative importance and possible redundancy of individual DAMPs is unknown; the relevance of ROS and TXNIP in NLRP3 activation in vivo remains unclear and contested; whether RAGE and other non-PRRs have a primary or secondary role in human disease is unknown; and the clinical studies cited (10 gout patients; 70 type 2 diabetes patients) were small and not designed to determine optimal dosing, duration or long-term outcomes.
- Evident from the text: the review is largely built on mouse models, and the authors repeatedly note that human relevance for NLRP3 in type 2 diabetes, RAGE in atherosclerosis and Alzheimer's disease, and CLEC4E/CLEC9A in sterile inflammation remains to be determined.
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Claims the paper makes
145 Not checked yet · 24 Own interpretation · 10 No basis given · 1 Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Although the clinical study was small, with only ten patients evaluated, all ten patients treated with anakinra had significant relief from symptoms108.”
§ Sterile inflammation: sensing and reacting to damage > Implications for therapy
What the sources say
- Supportedcites [108] So, A., De Smedt, T., Revaz, S. & Tschopp, J. A pilot study of IL-1 inhibition by anakinra in acute gout. Arthritis Res. Ther. 9, R28 (2007). source
The Conclusion describes this as a pilot study involving 10 patients with gouty arthritis, supporting the characterization of the clinical study as small. The Methods describe how those patients’ clinical outcomes were assessed. (LLM, conf=0.95)
plainn = 10- Asserted: passes — The authors put it forward as true.
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In the paper
“In ischaemia–reperfusion injury, as seen with myocardial infarction and stroke, the restoration of blood flow causes further tissue destruction as a result of neutrophilic infiltration, enhanced production of ROS and inflammatory responses to necrotic cells2.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
What the sources say
- Not checked yetcites [2] Cotran, R. S., Kumar, V. & Robbins, S. in Robbins Pathologic Basis of Disease (ed. Schoen, F. J.) 6–11 (W. B. Saunders Company, Philadelphia, 1994).
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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
“It is now apparent that these same PRRs can also be activated by non-microbial signals, many of which are considered as damage-associated molecular patterns.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
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In the paper
“Sterile inflammation has also been implicated in such disease processes as gout and pseudogout, in which the deposition of monosodium urate (MSU) and calcium pyrophosphate dihydrate (CPPD) crystals in the joints results in acute neutrophilic infiltration followed by chronic inflammation, fibrosis and cartilage destruction3.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
What the sources say
- Not checked yetcites [3] Cotran, R. S., Kumar, V. & Robbins, S . in Robbins Pathologic Basis of Disease (ed. Schoen, F. J.) 1255–1259 (W. B. Saunders Company, Philadelphia, 1994).
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Chronic inhalation of sterile irritants, such as asbestos and silica, can lead to persistent activation of alveolar macrophages and result in pulmonary interstitial fibrosis1.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
What the sources say
- Not checked yetcites [1] Mossman, B. T. & Churg, A. Mechanisms in the pathogenesis of asbestosis and silicosis. Am. J. Respir. Crit. Care Med. 157, 1666–1680 (1998). source
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In the paper
“For example, there is evidence for a role of TLR2 and/or TLR4 in the induction of cytokine and chemokine production in response to extracellular matrix components, including hyaluronan fragments or soluble proteoglycan components, in vitro and in vivo31–34.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
What the sources say
- Not checked yetcites [31] Jiang, D. et al. Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nature Med. 11, 1173–1179 (2005). This paper shows the dual role of TLRs in mediating sterile inflammation in response to hyaluronan fragments released during injury and in promoting tissue repair. source
- Not checked yetcites [32] Scheibner, K. A. et al. Hyaluronan fragments act as an endogenous danger signal by engaging TLR2. J. Immunol. 177, 1272–1281 (2006). source
- Not checked yetcites [33] Schaefer, L. et al. The matrix component biglycan is proinflammatory and signals through Toll-like receptors 4 and 2 in macrophages. J. Clin. Invest. 115, 2223–2233 (2005). source
- Not checked yetcites [34] Kim, S. et al. Carcinoma-produced factors activate myeloid cells through TLR2 to stimulate metastasis. Nature 457, 102–106 (2009). source
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In the paper
“There is mounting evidence that TLRs sense endogenous molecules in addition to microbial PAMPs.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
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In the paper
“Moreover, inflammatory responses during infection are very similar to responses induced by sterile stimuli, including the recruitment of neutrophils and macrophages, the production of inflammatory cytokines and chemokines, and the induction of T cell-mediated adaptive immune responses23.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation
What the sources say
- Not checked yetcites [23] Mbitikon-Kobo, F. M. et al. Characterization of a CD44/CD122int memory CD8 T cell subset generated under sterile inflammatory conditions. J. Immunol. 182, 3846–3854 (2009). source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“In one study, treatment of mice with HMGb1-specific antibodies during acetaminophen-induced liver necrosis ameliorated inflammatory cell recruitment10.”
§ Sterile inflammation: sensing and reacting to damage > DAMPs: indicators of tissue injury
What the sources say
- Not checked yetcites [10] Scaffidi, P., Misteli, T. & Bianchi, M. E. Release of chromatin protein HMGB1 by necrotic cells triggers inflammation. Nature 418, 191–195 (2002). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Sterile inflammation is also an important component of atherosclerosis, as engulfment of cholesterol crystals by macrophages leads to the activation and recruitment of inflammatory cells, endothelial cell dysfunction and plaque formation5.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
What the sources say
- Not checked yetcites [5] Ross, R. Atherosclerosis — an inflammatory disease. N. Engl. J. Med. 340, 115–126 (1999). source
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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 sterile inflammation that ensues either resolves the initial insult or leads to disease.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
plaindirect- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper may give no reason why it holds. It may state two separate claims as one.
In the paper
“However, uric acid depletion does not completely eliminate acetaminophen-induced liver inflammation or the adjuvant activity of damaged cells, which may reflect residual uric acid following depletion or redundant activities by other DAMPs.”
§ Sterile inflammation: sensing and reacting to damage > DAMPs: indicators of tissue injury
What the sources say
- Not checked yetcites [13] Kono, H., Chen, C. J., Ontiveros, F. & Rock, K. L. Uric acid promotes an acute inflammatory response to sterile cell death in mice. J. Clin. Invest. 120, 1939–1949 (2010). source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Tlr2 and Tlr4 double-knockout mice exhibit impaired transepithelial recruitment of inflammatory cells and decreased survival in response to lung injury31.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
What the sources say
- Not checked yetcites [31] Jiang, D. et al. Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nature Med. 11, 1173–1179 (2005). This paper shows the dual role of TLRs in mediating sterile inflammation in response to hyaluronan fragments released during injury and in promoting tissue repair. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“by contrast, in particulate-induced sterile inflammation, uric acid depletion had no effect, suggesting that uric acid may be a major pro-inflammatory DAMP that is specifically involved in cell death-related sterile inflammation13.”
§ Sterile inflammation: sensing and reacting to damage > DAMPs: indicators of tissue injury
What the sources say
- Not checked yetcites [13] Kono, H., Chen, C. J., Ontiveros, F. & Rock, K. L. Uric acid promotes an acute inflammatory response to sterile cell death in mice. J. Clin. Invest. 120, 1939–1949 (2010). source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“TLR4, specifically, has been shown to mediate inflammatory responses to free fatty acids, which are elevated in obesity and are associated with insulin resistance38.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
What the sources say
- Not checked yetcites [38] Shi, H. et al. TLR4 links innate immunity and fatty acid-induced insulin resistance. J. Clin. Invest. 116, 3015–3025 (2006). source
boosteddirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Similarly, TLR3 can sense endogenous RNA derived from necrotic neutrophils, which contributes to the inflammatory response elicited by necrosis in the bowel39.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
What the sources say
- Not checked yetcites [39] Cavassani, K. A. et al. TLR3 is an endogenous sensor of tissue necrosis during acute inflammatory events. J. Exp. Med. 205, 2609–2621 (2008). source
plaindirect- Asserted: passes — The authors put it forward as true.
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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
“Although these factors are not conventionally considered as DAMPs, they can mediate sterile inflammatory responses (see below).”
§ Sterile inflammation: sensing and reacting to damage > DAMPs: indicators of tissue injury
plaindirect- Asserted: passes — The authors put it forward as true.
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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, understanding the mechanisms of sterile inflammation is important for devising treatment strategies against various human diseases.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. It may be too vague to check against evidence.
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
“based on our current understanding, we propose three, not necessarily mutually exclusive, mechanisms by which sterile endogenous stimuli trigger inflammation: activation of PRRs by mechanisms similar to those used by microorganisms and PAMPs; release of intracellular cytokines and chemokines, such as IL-1α, that activate common pathways downstream of PRRs; and direct activation by receptors that”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation
hedgeddirect- Asserted: passes — The authors put it forward as true.
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- The authors state this as an assumption: The three proposed mechanisms by which sterile endogenous stimuli trigger inflammation are not necessarily mutually exclusive.
In the paper
“It is now evident that PRRs also recognize non-infectious material that can cause tissue damage and endogenous molecules that are released during cellular injury (TABLE 1).”
§ Sterile inflammation: sensing and reacting to damage > Abstract
What the sources say
- Not checked yetcites TABLE 1
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Finally, immune cell infiltration in the absence of microorganisms is also characteristic of tumours, and these cells can influence the growth and progression of cancer6.”
§ Sterile inflammation: sensing and reacting to damage > Abstract
What the sources say
- Not checked yetcites [6] Coussens, L. M. & Werb, Z. Inflammation and cancer. Nature 420, 860–867 (2002). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“DAMPs have been identified by their ability to induce inflammatory responses in vitro and/orin vivo when purified and by the observed reduction in inflammation when they are selectively depleted17.”
§ Sterile inflammation: sensing and reacting to damage > DAMPs: indicators of tissue injury
What the sources say
- Not checked yetcites [17] Kono, H. & Rock, K. L. How dying cells alert the immune system to danger. Nature Rev. Immunol. 8, 279–289 (2008). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Interestingly, the anti-diabetic drug glyburide (Glibenclamide; Roche/Sanofi-Aventis) has been shown to block glucose-mediated secretion of IL-1β by mouse pancreatic islets62, as well as IL-1β production by macrophages in response to IAPP61, and NLRP3-deficient mice were more glucose tolerant than wild-type mice62.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [61] Masters, S. L. et al. Activation of the NLRP3 inflammasome by islet amyloid polypeptide provides a mechanism for enhanced IL-1β in type 2 diabetes. Nature Immunol. 11, 897–904 (2010). source
- Not checked yetcites [62] Zhou, R., Tardivel, A., Thorens, B., Choi, I. & Tschopp, J. Thioredoxin-interacting protein links oxidative stress to inflammasome activation. Nature Immunol. 11, 136–140 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Importantly, NLRP3-dependent caspase 1 activation was associated with destabilization of the lysosomal membrane and activation of lysosomal proteases (specifically, cathepsin b)44.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [44] Hornung, V. et al. Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization. Nature Immunol. 9, 847–856 (2008). This study was pivotal in providing a model of NLRP3 activation that involves lysosomal damage and cathepsin B activation. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“Compared with wild-type mice, IL-1R-deficient mice had decreased neutrophilic infiltration and inflammation in the liver after acetaminophen-induced liver injury22 and in the lungs after exposure to silica44.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [22] Chen, C. J. et al. Identification of a key pathway required for the sterile inflammatory response triggered by dying cells. Nature Med. 13, 851–856 (2007). This paper demonstrates a crucial role for IL-1α in sterile inflammation and, in particular, neutrophil recruitment induced by necrotic cells. source
- Not checked yetcites [44] Hornung, V. et al. Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization. Nature Immunol. 9, 847–856 (2008). This study was pivotal in providing a model of NLRP3 activation that involves lysosomal damage and cathepsin B activation. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“NLRP3 signalling has been shown to involve at least two steps, the first involving PRR- or cytokine-dependent transcriptional upregulation of NLRP3 and the second involving activation of the NLRP3 inflammasome, which leads to IL-1β production53,54 (BOX 4).”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [53] Bauernfeind, F. G. et al. Cutting edge: NF-κB activating pattern recognition and cytokine receptors license NLRP3 inflammasome activation by regulating NLRP3 expression. J. Immunol. 183, 787–791 (2009). source
- Not checked yetcites [54] Franchi, L., Eigenbrod, T. & Nunez, G. Cutting edge: TNF-α mediates sensitization to ATP and silica via the NLRP3 inflammasome in the absence of microbial stimulation. J. Immunol. 183, 792–796 (2009). References 53 and 54 provide evidence that the first signal, or priming event, necessary for activation of the NLRP3 inflammasome involves upregulation of NLRP3 expression by NF-κB through the action of TLRs or pro-inflammatory cytokines such as TNF. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Furthermore, TLRs seem to function redundantly with other signalling pathways, so the contribution of TLRs to the overall sterile inflammatory response remains unclear.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
hedged- Asserted: passes — The authors put it forward as true.
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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
“However, the amounts of ATP necessary for NLRP3-mediated caspase 1 activation to be detected in macrophages in vitro are greater than physiological concentrations63 and, therefore, the relevance of this pathway in vivo is uncertain.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [63] el-Moatassim, C. & Dubyak, G. R. A novel pathway for the activation of phospholipase D by P2z purinergic receptors in BAC1.2F5 macrophages. J. Biol. Chem. 267, 23664–23673 (1992). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“elevated levels of IL-1β are also observed in the pancreatic islet cells from patients with type 2 diabetes46, which is increasingly being recognized as having a strong inflammatory component47.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [46] Boni-Schnetzler, M. et al. Increased interleukin (IL)-1β messenger ribonucleic acid expression in β-cells of individuals with type 2 diabetes and regulation of IL-1β in human islets by glucose and autostimulation. J. Clin. Endocrinol. Metab. 93, 4065–4074 (2008). source
- Not checked yetcites [47] Shoelson, S. E., Lee, J. & Goldfine, A. B. Inflammation and insulin resistance. J. Clin. Invest. 116, 1793–1801 (2006). source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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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, it has been suggested that NLRP3 senses intracellular K + depletion, which may act as a surrogate marker of cellular injury that is sensed by NLRP3.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
hedgedconditional- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. It may state two separate claims as one.
In the paper
“However, IL-1β secretion was only partially dependent on P2RX7, suggesting that the release of ATP may be only one mechanism by which necrotic cells can activate NLRP3.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [60] Iyer, S. S. et al. Necrotic cells trigger a sterile inflammatory response through the Nlrp3 inflammasome. Proc. Natl Acad. Sci. USA 106, 20388–20393 (2009). source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“ATP binds to purinergic receptor P2X7 (P2RX7), which leads to the opening of an ATP-gated cation channel that induces K + efflux and the formation of a large pore mediated by the hemichannel protein pannexin 1 (REFS 64,65).”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [64] Pelegrin, P. & Surprenant, A. Pannexin-1 mediates large pore formation and interleukin-1β release by the ATP-gated P2X7 receptor. EMBO J. 25, 5071–5082 (2006). source
- Not checked yetcites [65] Locovei, S., Wang, J. & Dahl, G. Activation of pannexin 1 channels by ATP through P2Y receptors and by cytoplasmic calcium. FEBS Lett. 580, 239–244 (2006). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“In atherosclerosis, engulfment of cholesterol by macrophages leads to IL-1β production, which can stimulate the production of platelet-derived growth factor, promotion of smooth muscle cell and fibroblast proliferation, arterial wall thickening and plaque formation5,45.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [5] Ross, R. Atherosclerosis — an inflammatory disease. N. Engl. J. Med. 340, 115–126 (1999). source
- Not checked yetcites [45] Raines, E. W., Dower, S. K. & Ross, R. Interleukin-1 mitogenic activity for fibroblasts and smooth muscle cells is due to PDGF-AA. Science 243, 393–396 (1989). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Collectively, the evidence suggests that endogenous stimuli can induce a sterile inflammatory response through TLRs, although the precise molecules that engage TLRs remain poorly defined.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: recognition of endogenous DAMPs by TLRs
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In the paper
“IL-1β is a potent pro-inflammatory cytokine that is produced mainly by macrophages and has many biological functions that are important in sterile inflammation, such as the upregulation of those adhesion molecules on endothelial cells that are important for the recruitment of neutrophils and monocytes42 and for the induction of additional pro-inflammatory mediators43.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [42] Wang, X., Feuerstein, G. Z., Gu, J. L., Lysko, P. G. & Yue, T. L. Interleukin-1β induces expression of adhesion molecules in human vascular smooth muscle cells and enhances adhesion of leukocytes to smooth muscle cells. Atherosclerosis 115, 89–98 (1995). source
- Not checked yetcites [43] Gabay, C., Lamacchia, C. & Palmer, G. IL-1 pathways in inflammation and human diseases. Nature Rev. Rheumatol. 6, 232–241 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Low-density lipoprotein (LDL) receptor-deficient mice, which are prone to developing atherosclerotic lesions, had lower IL-1β levels, smaller atherosclerotic lesions and less neutrophilic infiltration than wild-type mice when lethally irradiated and infused with NLRP3-deficient bone marrow59.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [59] Duewell, P. et al. NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals. Nature 464, 1357–1361 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“IL-1, which includes both IL-1α and IL-1β, is a key mediator of sterile inflammation that acts through the IL-1 receptor (IL-1R)22,41.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [22] Chen, C. J. et al. Identification of a key pathway required for the sterile inflammatory response triggered by dying cells. Nature Med. 13, 851–856 (2007). This paper demonstrates a crucial role for IL-1α in sterile inflammation and, in particular, neutrophil recruitment induced by necrotic cells. source
- Not checked yetcites [41] Kono, H., Karmarkar, D., Iwakura, Y. & Rock, K. L. Identification of the cellular sensor that stimulates the inflammatory response to sterile cell death. J. Immunol. 184, 4470–4478 (2010). This study shows the crucial role for macrophages in mediating the inflammatory response to sterile cell death, such as by IL-1α production. source
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In the paper
“Lysosomal damage can occur during cellular injury and necrosis, and has also been associated with other sterile activators of NLRP3, such as cholesterol59 and silica crystals44.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [59] Duewell, P. et al. NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals. Nature 464, 1357–1361 (2010). source
- Not checked yetcites [44] Hornung, V. et al. Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization. Nature Immunol. 9, 847–856 (2008). This study was pivotal in providing a model of NLRP3 activation that involves lysosomal damage and cathepsin B activation. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“NLRP3-deficient mice were also less susceptible to renal ischaemia–reperfusion injuries induced by bilateral renal artery ligation and to acetaminophen-induced hepatotoxicity40,60.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [40] Imaeda, A. B. et al. Acetaminophen-induced hepatotoxicity in mice is dependent on Tlr9 and the Nalp3 inflammasome. J. Clin. Invest. 119, 305–314 (2009).
- Not checked yetcites [60] Iyer, S. S. et al. Necrotic cells trigger a sterile inflammatory response through the Nlrp3 inflammasome. Proc. Natl Acad. Sci. USA 106, 20388–20393 (2009). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“In general, the ligands of these CLRs are unknown70.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: an emerging role for CLRs
What the sources say
- Not checked yetcites [70] Geijtenbeek, T. B. & Gringhuis, S. I. Signalling through C-type lectin receptors: shaping immune responses. Nature Rev. Immunol. 9, 465–479 (2009). source
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
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 class of PRRs contains a carbohydrate-binding domain that recognizes carbohydrates on viruses, bacteria and fungi.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: an emerging role for CLRs
plaindirect- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Using a model of peritonitis triggered by necrotic cells, IL-1α was shown to be important for the recruitment of neutrophils, which was caspase 1 independent, and this response was impaired in mice lacking IL-1R expression by non-myeloid cells22.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
What the sources say
- Not checked yetcites [22] Chen, C. J. et al. Identification of a key pathway required for the sterile inflammatory response triggered by dying cells. Nature Med. 13, 851–856 (2007). This paper demonstrates a crucial role for IL-1α in sterile inflammation and, in particular, neutrophil recruitment induced by necrotic cells. source
plaindirect- Asserted: passes — The authors put it forward as true.
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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
“CLRs are an increasingly recognized category of PRRs that are important in host defence.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: an emerging role for CLRs
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“In particular, C-type lectin 4e (CLeC4e; also known as MINCLe) can detect the DAMP spliceosome-associated protein 130 (SAP130), which is a component of a small nuclear ribonucleo protein that can be released by necrotic but not apoptotic cells, resulting in upregulation of pro-inflammatory mediators such as CXC-chemokine ligand 2 (CXCL2) and in neutrophil recruitment73.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: an emerging role for CLRs
What the sources say
- Not checked yetcites [73] Cambi, A. & Figdor, C. Necrosis: C-type lectins sense cell death. Curr. Biol. 19, R375–R378 (2009). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Therefore, it may be involved in regulating sterile immune responses, although the specific ligand recognized in this case is still unknown73,75.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: an emerging role for CLRs
What the sources say
- Not checked yetcites [73] Cambi, A. & Figdor, C. Necrosis: C-type lectins sense cell death. Curr. Biol. 19, R375–R378 (2009). source
- Not checked yetcites [75] Sancho, D. et al. Identification of a dendritic cell receptor that couples sensing of necrosis to immunity. Nature 458, 899–903 (2009). This paper showed a role for CLEC9A in regulating immune responses to sterile cell death, specifically through the cross-presentation of dead cell-associated antigens. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Silica58,68, asbestos57 and ATP69 have all been associated with ROS production, and ROS inhibition in vitro resulted in impairment of caspase 1 activation and IL-1β production by these stimuli57,58,69.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [57] Dostert, C. et al. Innate immune activation through Nalp3 inflammasome sensing of asbestos and silica. Science 320, 674–677 (2008). This study led to the model of NLRP3 activation that is dependent on the sensing of ROS, and demonstrated a role for NLRP3 in asbestosis. source
- Not checked yetcites [58] Cassel, S. L. et al. The Nalp3 inflammasome is essential for the development of silicosis. Proc. Natl Acad. Sci. USA 105, 9035–9040 (2008). source
- Not checked yetcites [68] Fubini, B. & Hubbard, A. Reactive oxygen species (ROS) and reactive nitrogen species (RNS) generation by silica in inflammation and fibrosis. Free Radic. Biol. Med. 34, 1507–1516 (2003). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“evidence to support this are the observations that artificial lysosomal rupture alone can activate NLRP3 and that pharmacological inhibition or genetic depletion of cathepsin b results in inhibition of caspase 1 activation, although this inhibition was only partial44,56,59.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [44] Hornung, V. et al. Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization. Nature Immunol. 9, 847–856 (2008). This study was pivotal in providing a model of NLRP3 activation that involves lysosomal damage and cathepsin B activation. source
- Not checked yetcites [56] Halle, A. et al. The NALP3 inflammasome is involved in the innate immune response to amyloid-β. Nature Immunol. 9, 857–865 (2008). source
- Not checked yetcites [59] Duewell, P. et al. NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals. Nature 464, 1357–1361 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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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
“Collectively, there is still controversy regarding the roles of the individual model pathways for NLRP3 activation, and it remains to be determined whether there is a common mechanism by which numerous heterogeneous stimuli converge on NLRP3.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
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In the paper
“when cells die by necrosis, such as during injury, this precursor form of IL-1α is released, leading to activation of its cognate receptor and rapid recruitment of inflammatory cells into the surrounding injured tissue22,78.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
What the sources say
- Not checked yetcites [22] Chen, C. J. et al. Identification of a key pathway required for the sterile inflammatory response triggered by dying cells. Nature Med. 13, 851–856 (2007). This paper demonstrates a crucial role for IL-1α in sterile inflammation and, in particular, neutrophil recruitment induced by necrotic cells. source
- Not checked yetcites [78] Cohen, I. et al. Differential release of chromatin-bound IL-1α discriminates between necrotic and apoptotic cell death by the ability to induce sterile inflammation. Proc. Natl Acad. Sci. USA 107, 2574–2579 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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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
“Therefore, it is possible that divergent upstream danger signals that are sensed by NLRP3 may converge on lysosomal damage and cathepsin b activation.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
hedgedconditional- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim.
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In the paper
“Unlike its related family members IL-1β and IL-18, IL-1α is synthesized as a biologically active cytokine in its full-length precursor form and does not require processing for signalling through IL-1R78,79.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
What the sources say
- Not checked yetcites [78] Cohen, I. et al. Differential release of chromatin-bound IL-1α discriminates between necrotic and apoptotic cell death by the ability to induce sterile inflammation. Proc. Natl Acad. Sci. USA 107, 2574–2579 (2010). source
- Not checked yetcites [79] Dinarello, C. A. IL-1: discoveries, controversies and future directions. Eur. J. Immunol. 40, 599–606 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“In this study, TXNIP-deficient mice had impaired IL-1β production and neutrophil influx after intraperitoneal injection of MSU crystals, and TXNIP-deficient macrophages had decreased IL-1β production in response to a range of known NLRP3 activators, including MSU crystals, silica, and ATP62.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: generation of IL-1β by inflammasomes
What the sources say
- Not checked yetcites [62] Zhou, R., Tardivel, A., Thorens, B., Choi, I. & Tschopp, J. Thioredoxin-interacting protein links oxidative stress to inflammasome activation. Nature Immunol. 11, 136–140 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“This is in contrast with apoptotic cells, in which IL-1α is sequestered intracellularly78, or with intact cells, in which the secretion of mature IL-1α is partially dependent on caspase 1 activity80–82.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
What the sources say
- Not checked yetcites [78] Cohen, I. et al. Differential release of chromatin-bound IL-1α discriminates between necrotic and apoptotic cell death by the ability to induce sterile inflammation. Proc. Natl Acad. Sci. USA 107, 2574–2579 (2010). source
- Not checked yetcites [80] Li, P. et al. Mice deficient in IL-1β-converting enzyme are defective in production of mature IL-1β and resistant to endotoxic shock. Cell 80, 401–411 (1995). source
- Not checked yetcites [81] Kuida, K. et al. Altered cytokine export and apoptosis in mice deficient in interleukin-1β converting enzyme. Science 267, 2000–2003 (1995). source
- Not checked yetcites [82] Keller, M., Ruegg, A., Werner, S. & Beer, H. D. Active caspase-1 is a regulator of unconventional protein secretion. Cell 132, 818–831 (2008). source
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“CLeC9A has been shown to recognize necrotic cells and induce the cross-presentation of dead cell-associated antigens to CD8+ T cells.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Role of PRRs: an emerging role for CLRs
What the sources say
- Not checked yetcites [73] Cambi, A. & Figdor, C. Necrosis: C-type lectins sense cell death. Curr. Biol. 19, R375–R378 (2009). source
- Not checked yetcites [75] Sancho, D. et al. Identification of a dendritic cell receptor that couples sensing of necrosis to immunity. Nature 458, 899–903 (2009). This paper showed a role for CLEC9A in regulating immune responses to sterile cell death, specifically through the cross-presentation of dead cell-associated antigens. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“These products can accumulate under conditions of high oxidant stress and are found at elevated levels in chronic inflammatory disease states such as type 1 diabetes92.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [92] Bucciarelli, L. G. et al. RAGE is a multiligand receptor of the immunoglobulin superfamily: implications for homeostasis and chronic disease. Cell. Mol. Life Sci. 59, 1117–1128 (2002). source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“Apoe–/–Rage–/– mice also exhibited a reduction in atherosclerosis101, as shown by a reduction in both atherosclerotic plaque formation and production of pro-inflammatory mediators within the aorta.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [101] Harja, E. et al. Vascular and inflammatory stresses mediate atherosclerosis via RAGE and its ligands in apoE−/− mice. J. Clin. Invest. 118, 183–194 (2008). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“In addition to AGes, RAGe also recognizes HMGb193 and the S100 family members19, which are released during cellular stress and necrotic cell death, and β-amyloid94, the accumulation of which is pathogenic in Alzheimer's disease.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [94] Yan, S. D. et al. RAGE and amyloid-β peptide neurotoxicity in Alzheimer's disease. Nature 382, 685–691 (1996). source
plaindirect- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Thus, the release of IL-1α from certain cells, such as dendritic cells, contributes to sterile inflammation, but macrophages seem to be the primary sentinel cells that mediate the sensing of necrotic cells through the production of mature IL-1α and IL-1β41.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
What the sources say
- Not checked yetcites [41] Kono, H., Karmarkar, D., Iwakura, Y. & Rock, K. L. Identification of the cellular sensor that stimulates the inflammatory response to sterile cell death. J. Immunol. 184, 4470–4478 (2010). This study shows the crucial role for macrophages in mediating the inflammatory response to sterile cell death, such as by IL-1α production. source
hedgeddirect- Asserted: passes — The authors put it forward as true.
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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
“Collectively, the evidence suggests that the precursor forms of IL-1α and IL-33 (both of which are biologically active) are preferentially released during necrosis to alert the immune system to cell damage, leading to the initiation of the healing response.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
hedgeddirect- Asserted: passes — The authors put it forward as true.
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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
“These studies suggest that the precursor form of IL-1α that is released by necrotic cells contributes to the initial neutrophilic response, but resident macrophages are the main source of mature IL-1α and IL-1β, which are needed for cell death-induced sterile inflammation (FIG. 3).”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
hedgeddirect- Asserted: passes — The authors put it forward as true.
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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, IL-33, which is expressed at high levels by endothelial cells and some epithelial cells, is expected to be active when it is released during necrosis, but not apoptosis, which is associated with executioner caspase activation.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Release of intracellular cytokines
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“How CD44 signalling contributes to sterile inflammation is unclear, but it has been shown to physically interact with TLR4 in vitro and function as an accessory molecule for TLR4 signalling in response to hyaluronan102,103.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [102] Jiang, D., Liang, J. & Noble, P. W. Hyaluronan in tissue injury and repair. Annu. Rev. Cell Dev. Biol. 23, 435–461 (2007). source
- Not checked yetcites [103] Taylor, K. R. et al. Recognition of hyaluronan released in sterile injury involves a unique receptor complex dependent on Toll-like receptor 4, CD44, and MD-2. J. Biol. Chem. 282, 18265–18275 (2007). source
plaindirect- Asserted: passes — The authors put it forward as true.
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None of the sources cited for this claim have been checked yet.
In the paper
“In addition to AGes, RAGe also recognizes HMGb193 and the S100 family members19, which are released during cellular stress and necrotic cell death, and β-amyloid94, the accumulation of which is pathogenic in Alzheimer's disease.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [19] Hofmann, M. A. et al. RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides. Cell 97, 889–901 (1999). source
- Not checked yetcites [93] Hori, O. et al. The receptor for advanced glycation end products (RAGE) is a cellular binding site for amphoterin. Mediation of neurite outgrowth and co-expression of rage and amphoterin in the developing nervous system. J. Biol. Chem. 270, 25752–25761 (1995). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“CD24-mediated inhibition was associated with increased pro-inflammatory cytokine production by HMGb1 and decreased survival following acetaminophen-induced liver injury106.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [106] Chen, G. Y., Tang, J., Zheng, P. & Liu, Y. CD24 and Siglec-10 selectively repress tissue damage-induced immune responses. Science 323, 1722–1725 (2009). source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“Those treated with anakinra had improved glucose levels and reduced systemic inflammation, as suggested by lower circulating levels of inflammatory markers, such as IL-6 and C-reactive protein.”
§ Sterile inflammation: sensing and reacting to damage > Implications for therapy
What the sources say
- Not checked yetcites [109] Larsen, C. M. et al. Interleukin-1-receptor antagonist in type 2 diabetes mellitus. N. Engl. J. Med. 356, 1517–1526 (2007). source
hedgeddirectn = 70- Asserted: passes — The authors put it forward as true.
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In the paper
“Similarly, CD36 is a scavenger receptor that binds oxidized LDL and β-amyloid, which are associated with sterile inflammation related to atherosclerosis and Alzheimer's disease, respectively.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
What the sources say
- Not checked yetcites [104] Hoebe, K. et al. CD36 is a sensor of diacylglycerides. Nature 433, 523–527 (2005). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Indeed, mice deficient in TLR2 and TLR4 expression had increased mortality in response to hypoxia-induced lung injury, which was associated with decreased integrity of the lung epithelium31.”
§ Sterile inflammation: sensing and reacting to damage > Implications for therapy
What the sources say
- Not checked yetcites [31] Jiang, D. et al. Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nature Med. 11, 1173–1179 (2005). This paper shows the dual role of TLRs in mediating sterile inflammation in response to hyaluronan fragments released during injury and in promoting tissue repair. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“TLR4 signalling was found to be important for dendritic cell-mediated cross-presentation of tumour antigens from dying, chemotherapy-treated tumour cells and involved HMGb1 release from the dying cells115.”
§ Sterile inflammation: sensing and reacting to damage > Implications for therapy
What the sources say
- Not checked yetcites [115] Apetoh, L. et al. Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy. Nature Med. 13, 1050–1059 (2007). This paper showed the importance of TLR4 signalling in response to DAMPs derived from tumour cell death after chemotherapy or radiation treatment during the induction of host immune responses that are important for inhibiting tumour growth. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Furthermore, chemotherapy-treated tumour cells injected into wild-type mice inhibited tumour development when the mice were rechallenged with tumour cells, but this effect was abrogated in NLRP3-deficient and P2RX7-deficient mice112, suggesting that NLRP3-mediated IL-1β production through the ATP–P2RX7 pathway is important for immune surveillance against tumours.”
§ Sterile inflammation: sensing and reacting to damage > Implications for therapy
What the sources say
- Not checked yetcites [112] Ghiringhelli, F. et al. Activation of the NLRP3 inflammasome in dendritic cells induces IL-1β-dependent adaptive immunity against tumors. Nature Med. 15, 1170–1178 (2009). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“However, the clinical study was still small and was not designed to determine optimal dosing, duration of use or long-term outcomes in disease control.”
§ Sterile inflammation: sensing and reacting to damage > Implications for therapy
What the sources say
- Not checked yetcites [109] Larsen, C. M. et al. Interleukin-1-receptor antagonist in type 2 diabetes mellitus. N. Engl. J. Med. 356, 1517–1526 (2007). source
plainn = 70- 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
“Similarly, CD36 is a scavenger receptor that binds oxidized LDL and β-amyloid, which are associated with sterile inflammation related to atherosclerosis and Alzheimer's disease, respectively.”
§ Sterile inflammation: sensing and reacting to damage > Mechanisms of sterile inflammation > Non-PRR-mediated recognition of DAMPs
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.
The paper relies on this without support.
Sterile inflammation is marked by the recruitment of neutrophils and macrophages and the production of pro-inflammatory cytokines and chemokines, notably tumour necrosis factor (TNF) and interleukin-1 (IL-1).
“Similar to microbially induced inflammation, sterile inflammation is marked by the recruitment of neutrophils and macrophages and the production of pro-inflammatory cytokines and chemokines, notably tumour necrosis factor (TNF) and interleukin-1 (IL-1).”
The paper relies on this without support.
DAMPs are endogenous factors that are normally sequestered intracellularly and are therefore hidden from recognition by the immune system under normal physiological conditions.
“A common feature of DAMPs is that they are endogenous factors that are normally sequestered intracellularly and are therefore hidden from recognition by the immune system under normal physiological conditions.”
The paper relies on this without support.
Under conditions of cellular stress or injury, DAMPs can be released into the extracellular environment by dying cells and trigger inflammation under sterile conditions.
“However, under conditions of cellular stress or injury, these molecules can then be released into the extracellular environment by dying cells and trigger inflammation under sterile conditions.”
The paper relies on this without support.
The type of cell death affects its immunogenicity and its ability to release immunostimulatory DAMPs.
“The type of cell death notably affects its immunogenicity and ability to release immunostimulatory DAMPs.”
The paper relies on this without support.
Secretion of IL-1β by inflammatory cells is largely dependent on a multiprotein complex termed the inflammasome, of which the hallmark activity is the activation of caspase 1.
“The secretion of IL-1β by inflammatory cells is largely dependent on a multiprotein complex termed the inflammasome, of which the hallmark activity is the activation of caspase 1.”
The authors state this as an assumption.
The three proposed mechanisms by which sterile endogenous stimuli trigger inflammation are not necessarily mutually exclusive.
“based on our current understanding, we propose three, not necessarily mutually exclusive, mechanisms by which sterile endogenous stimuli trigger inflammation:”
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
“In addition, TLRs are activated by a wide array of endogenous molecules released from self-cells following tissue damage (known as damage-associated molecular pattern, DAMP) such as hyaluronic acid and molecules derived from necrotic and apoptotic cells including nucleic acids [42].”
From Ligand dependent restoration of human TLR3 signaling and death in p53 mutant cells (2016) · cites this paper as [42]
Experimental — accuracy not yet measuredIn the citing paper
“these current studies suggest that stressor exposure may also stimulate sterile inflammation in the brain, or neuroinflammation (Chen and Nunez, 2010).”
From Danger Signals and Inflammasomes: Stress-Evoked Sterile Inflammation in Mood Disorders (2017) · cites this paper as Chen and Nunez, 2010
In the citing paper
“In peritoneal dialysis and hemodialysis patients, CBT-I improved sleep quality compared with a sleep hygiene education intervention, which was paralleled by a decrease of serum levels of inflammatory markers, including IL-1 (102), CRP, and IL-18 (101).”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [101]
Citations
Cites
Atherosclerosis--an inflammatory disease
Ross, R. (1999) · New England Journal of Medicine · doi:10.1056/nejm199901143400207 · Cited by 21,725
Coussens, L. M., & Werb, Z. (2002) · Nature · doi:10.1038/nature01322 · Cited by 15,111
Pattern Recognition Receptors and Inflammation
Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895
Gout-associated uric acid crystals activate the NALP3 inflammasome
Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J. (2006) · Nature · doi:10.1038/nature04516 · Cited by 5,326
Tolerance, Danger and the Extended Family
Matzinger, P. (1994) · Annual Review of Immunology · doi:10.1146/annurev.iy.12.040194.005015 · Cited by 5,107
Inflammation and insulin resistance
Shoelson, S. E. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29069 · Cited by 4,769
(1980) · Annals of Internal Medicine · doi:10.7326/0003-4819-92-3-460_4 · Cited by 4,593
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251
Release of chromatin protein HMGB1 by necrotic cells triggers inflammation
Scaffidi, P., Misteli, T., & Bianchi, M. E. (2002) · Nature · doi:10.1038/nature00858 · Cited by 4,221
NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals
Duewell, P., Kono, H., Rayner, K. J., Sirois, C. M., Vladimer, G., Bauernfeind, F. G., Abela, G. S., Franchi, L., Nuñez, G., Schnurr, M., et al. (2010) · Nature · doi:10.1038/nature08938 · Cited by 4,026
Cited by
Sorted by citations
Items 101–200 of 1,013
Koushki, K., Shahbaz, S. K., Mashayekhi, K., Sadeghi, M., Zayeri, Z. D., Taba, M. Y., Banach, M., Al-Rasadi, K., Johnston, T. P., & Sahebkar, A. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-020-08791-9 · Cited by 382
Simmonds, S. J., Cuijpers, I., Heymans, S. R. B., & Jones, E. A. V. (2020) · Cells · doi:10.3390/cells9010242 · Cited by 399
Holditch, S. J., Brown, C. N., Lombardi, A. M., Nguyen, K. N., & Edelstein, C. L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20123011 · Cited by 387
Beclin-1-Dependent Autophagy Protects the Heart During Sepsis
Sun, Y., Yao, X., Zhang, Q.-J., Zhu, M., Liu, Z.-P., Ci, B., Xie, Y., Carlson, D., Rothermel, B. A., Sun, Y., et al. (2018) · Circulation · doi:10.1161/circulationaha.117.032821 · Cited by 381
Disease tolerance and immunity in host protection against infection
Soares, M. P., Teixeira, L., & Moita, L. F. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2016.136 · Cited by 376
Cell Death Mechanisms in Stroke and Novel Molecular and Cellular Treatment Options
Şekerdağ, E., Solaroğlu, İ., & Özdemir, Y. (2018) · Current Neuropharmacology · doi:10.2174/1570159x16666180302115544 · Cited by 381
Inflammasome, pyroptosis, and cytokines in myocardial ischemia-reperfusion injury
Toldo, S. A., Mauro, A. G., Cutter, Z., & Abbate, A. (2018) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00158.2018 · Cited by 377
Inflamm-aging of hematopoiesis, hematopoietic stem cells, and the bone marrow microenvironment
Kovtonyuk, L. V., Fritsch, K., Feng, X., Manz, M. G., & Takizawa, H. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00502 · Cited by 371
Chemokines in health and disease
Raman, D., Sobolik-Delmaire, T., & Richmond, A. J. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.01.005 · Cited by 387
Burguillos, M. A., Svensson, M., Schulte, T., Boza-Serrano, A., Garcia-Quintanilla, A., Kavanagh, E., Santiago, M., Viceconte, N., Oliva-Martin, M. J., Osman, A. M., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.02.012 · Cited by 365
Pyroptosis in health and disease: mechanisms, regulation and clinical perspective
Liu, Y., Pan, R., Ouyang, Y., Gu, W., Xiao, T., Yang, H., Tang, L. Y., Wang, H., Xiang, B., & Chen, P. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01958-2 · Cited by 391
The Roles of Mitochondrial Damage-Associated Molecular Patterns in Diseases
Nakahira, K., Hisata, S., & Choi, A. M. K. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6407 · Cited by 363
Cell death and infection: A double-edged sword for host and pathogen survival
Ashida, H., Mimuro, H., Ogawa, M., Kobayashi, T., Sanada, T., Kim, M., & Sasakawa, C. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201108081 · Cited by 377
Microparticles: biomarkers and beyond
Burger, D. E., Schock, S., Thompson, C. S., Montezano, A. C. I., Hakim, A. M., & Touyz, R. M. (2012) · Clinical Science · doi:10.1042/cs20120309 · Cited by 381
Recent progress in the development of fluorescent probes for imaging pathological oxidative stress
Geng, Y., Wang, Z., Zhou, J., Zhu, M., Liu, J., & James, T. D. (2023) · Chemical Society Reviews · doi:10.1039/d2cs00172a · Cited by 364
Oxidative Stress, Inflammation, and Disease
Chatterjee, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803269-5.00002-4 · Cited by 372
The HMGB1/RAGE axis triggers neutrophil-mediated injury amplification following necrosis
Huebener, P., Pradère, J., Hernandez, C., Gwak, G., Caviglia, J. M., Mu, X., Loike, J. D., Jenkins, R. E., Antoine, D. J., & Schwabe, R. F. (2014) · Journal of Clinical Investigation · doi:10.1172/jci76887 · Cited by 355
Huang, H., Evankovich, J. W., Yan, W., Nace, G., Zhang, L., Ross, M., Liao, X., Billiar, T. R., Xu, J., Esmon, C. T., et al. (2011) · Hepatology · doi:10.1002/hep.24501 · Cited by 351
Macrophages in Kidney Injury, Inflammation, and Fibrosis
Cao, Q., Harris, D. C. H., & Wang, Y. (2015) · Physiology · doi:10.1152/physiol.00046.2014 · Cited by 354
Dealing with danger in the CNS: the response of the immune system to injury
Gadani, S. P., Walsh, J. T., Lukens, J. R., & Kipnis, J. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.019 · Cited by 342
Immunopathophysiology of human sepsis
Wiersinga, W. J., & van der Poll, T. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104363 · Cited by 352
CD38: An Immunomodulatory Molecule in Inflammation and Autoimmunity
Piedra-Quintero, Z. L., Wilson, Z., Nava, P., & Guerau‐de‐Arellano, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.597959 · Cited by 351
Merline, R., Moreth, K., Beckmann, J., Nastase, M. V., Zeng-Brouwers, J., Tralhão, J. G., Lemarchand, P., Pfeilschifter, J., Schaefer, R. M., Iozzo, R. V., et al. (2011) · Science Signaling · doi:10.1126/scisignal.2001868 · Cited by 333
Marques, P. E., Amaral, S. S., Pires, D. A., Nogueira, L. L., Soriani, F. M., Lima, B. H. F., Lopes, G. A. O., Russo, R. C., Ávila, T. V., Melgaço, J. G., et al. (2012) · Hepatology · doi:10.1002/hep.25801 · Cited by 332
Muralidharan, S., & Mandrekar, P. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0313153 · Cited by 342
Adipose tissue aging: mechanisms and therapeutic implications
Ou, M., Zhang, H., Tan, P., Zhou, S., & Li, Q. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04752-6 · Cited by 352
Targeting the “Cytokine Storm” for Therapeutic Benefit
D’Elia, R. V., Harrison, K., Oyston, P. C. F., Lukaszewski, R. A., & Clark, G. C. (2013) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00636-12 · Cited by 328
Ischemia-Reperfusion Injury in Stroke
Nour, M., Scalzo, F., & Liebeskind, D. S. (2012) · Interventional Neurology · doi:10.1159/000353125 · Cited by 316
Aging and adipose tissue: potential interventions for diabetes and regenerative medicine
Palmer, A. K., & Kirkland, J. L. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.02.013 · Cited by 324
Macrophages: Supportive cells for tissue repair and regeneration
Chazaud, B. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.09.001 · Cited by 326
Lactoferrin in a Context of Inflammation-Induced Pathology
Kruzel, M. L., Zimecki, M., & Actor, J. K. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01438 · Cited by 308
Disulfide HMGB1 derived from platelets coordinates venous thrombosis in mice
Stark, K., Philippi, V., Stockhausen, S., Busse, J., Antonelli, A., Miller, M., Schubert, I., Hoseinpour, P., Chandraratne, S., von Brühl, M.-L., et al. (2016) · Blood · doi:10.1182/blood-2016-04-710632 · Cited by 306
Daniele, S. G., Béraud, D., Davenport, C., Cheng, K., Yin, H., & Maguire-Zeiss, K. A. (2015) · Science Signaling · doi:10.1126/scisignal.2005965 · Cited by 303
Oxidative stress, inflamm-aging and immunosenescence
Cannizzo, E. S., Clement, C. C., Sahu, R. K., Follo, C., & Santambrogio, L. (2011) · Journal of Proteomics · doi:10.1016/j.jprot.2011.06.005 · Cited by 315
Trimethylamine-N-Oxide Instigates NLRP3 Inflammasome Activation and Endothelial Dysfunction
Boini, K. M., Hussain, T., Li, P.-L., & Koka, S. S. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000484623 · Cited by 302
The HMGB1/RAGE axis triggers neutrophil-mediated injury amplification following necrosis
Huebener, P., Pradère, J., Hernandez, C., Gwak, G., Caviglia, J. M., Mu, X., Loike, J. D., Jenkins, R. E., Antoine, D. J., & Schwabe, R. F. (2019) · Journal of Clinical Investigation · doi:10.1172/jci126975 · Cited by 301
Emerging mechanisms of neutrophil recruitment across endothelium
Williams, M. R., Azcutia, V., Newton, G. A., Alcaide, P., & Luscinskas, F. W. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.06.009 · Cited by 310
The Role of Innate Immunity in Osteoarthritis: When Our First Line of Defense Goes On the Offensive
Orlowsky, E. W., & Kraus, V. B. (2015) · The Journal of Rheumatology · doi:10.3899/jrheum.140382 · Cited by 305
Self-associated molecular patterns mediate cancer immune evasion by engaging Siglecs on T cells
Stanczak, M. A., Siddiqui, S. S., Trefny, M. P., Thommen, D. S., Boligan, K. F., von Gunten, S., Tzankov, A., Tietze, L., Lardinois, D., Heinzelmann-Schwarz, V. A., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120612 · Cited by 300
Perivascular macrophages mediate neutrophil recruitment during bacterial skin infection
Abtin, A., Jain, R., Mitchell, A. J., Roediger, B., Brzoska, A. J., Tikoo, S., Cheng, Q., Ng, L. G., Cavanagh, L. L., von Andrian, U. H., et al. (2013) · Nature Immunology · doi:10.1038/ni.2769 · Cited by 307
Inflammation and mitochondrial dysfunction: A vicious circle in neurodegenerative disorders?
van Horssen, J., van Schaik, P. E. M., & Witte, M. E. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.06.050 · Cited by 298
Oxidative Stress and the Use of Antioxidants in Stroke
Shirley, R. B., Ord, E., & Work, L. M. (2014) · Antioxidants · doi:10.3390/antiox3030472 · Cited by 295
An inherited mutation in NLRC4 causes autoinflammation in human and mice
Kitamura, A., Sasaki, Y., Abe, T., Kano, H., & Yasutomo, K. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20141091 · Cited by 288
DAMPs as mediators of sterile inflammation in aging-related pathologies
Feldman, N., Rotter-Maskowitz, A., & Okun, E. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.01.003 · Cited by 283
The Role of Interferons in Inflammation and Inflammasome Activation
Kopitar-Jerala, N. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00873 · Cited by 260
Environmental concentrations of antibiotics impair zebrafish gut health
Zhou, L., Limbu, S. M., Shen, M., Zhai, W., Qiao, F., He, A., Du, Z., & Zhang, M. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2017.12.073 · Cited by 280
Extracellular ATP drives systemic inflammation, tissue damage and mortality
Cauwels, A., Rogge, E., Vandendriessche, B., Shiva, S., & Brouckaert, P. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.70 · Cited by 279
Vitiligo: Focus on Clinical Aspects, Immunopathogenesis, and Therapy
Boniface, K., Sénéschal, J., Picardo, M., & Taı̈eb, A. (2017) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-017-8622-7 · Cited by 275
Myokines: The endocrine coupling of skeletal muscle and bone
Gomarasca, M., Banfi, G., & Lombardi, G. (2019) · Advances in clinical chemistry · doi:10.1016/bs.acc.2019.07.010 · Cited by 283
Biological interplay between proteoglycans and their innate immune receptors in inflammation
Frey, H., Schroeder, N., Manon‐Jensen, T., Iozzo, R. V., & Schaefer, L. (2013) · FEBS Journal · doi:10.1111/febs.12145 · Cited by 281
AIM2 and NLRC4 inflammasomes contribute with ASC to acute brain injury independently of NLRP3
Dénes, Á., Coutts, G., Lénárt, N., Cruickshank, S. M., Pelegrín, P., Skinner, J., Rothwell, N. J., Allan, S. M., & Brough, D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1419090112 · Cited by 277
Oxidative Stress and Lung Ischemia-Reperfusion Injury
Ferrari, R. S., & Andrade, C. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/590987 · Cited by 278
Inflammatory Disequilibrium in Stroke
Petrovic‐Djergovic, D., Goonewardena, S. N., & Pinsky, D. J. (2016) · Circulation Research · doi:10.1161/circresaha.116.308022 · Cited by 271
Caspase-1: is IL-1 just the tip of the ICEberg?
Dénes, Á., López‐Castejón, G., & Brough, D. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.86 · Cited by 274
NF‐κB signalling pathways in nucleus pulposus cell function and intervertebral disc degeneration
Zhang, G., Liu, M., Chen, H., Wu, Z., Gao, Y., Ma, Z., He, X., & Kang, X. (2021) · Cell Proliferation · doi:10.1111/cpr.13057 · Cited by 265
Broekgaarden, M., Weijer, R., van Gulik, T. M., Hamblin, M. R., & Heger, M. (2015) · Cancer and Metastasis Reviews · doi:10.1007/s10555-015-9588-7 · Cited by 266
Mechanisms of lung ischemia-reperfusion injury
Laubach, V. E., & Sharma, A. K. (2016) · Current Opinion in Organ Transplantation · doi:10.1097/mot.0000000000000304 · Cited by 261
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Liu, D., Zeng, X., Xiao, L., Mehta, J. L., & Wang, X. (2017) · Basic Research in Cardiology · doi:10.1007/s00395-017-0663-9 · Cited by 260
Wu, J., Yan, Z., Schwartz, D. E., Yu, J., Malik, A. B., & Hu, G. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1200860 · Cited by 265
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Kzhyshkowska, J. G., Neyen, C. D., & Gordon, S. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.02.015 · Cited by 259
Tendon and ligament mechanical loading in the pathogenesis of inflammatory arthritis
Gracey, E., Burssens, A., Cambré, I., Schett, G. A., Lories, R. J. U., McInnes, I. B., Asahara, H., & Elewaut, D. S. (2020) · Nature Reviews Rheumatology · doi:10.1038/s41584-019-0364-x · Cited by 267
Pauwels, N., Bracke, K. R., Dupont, L., Pottelberge, G. R. V., Provoost, S., Berghe, T. V., Vandenabeele, P., Lambrecht, B. N., Joos, G., & Brusselle, G. (2011) · European Respiratory Journal · doi:10.1183/09031936.00158110 · Cited by 253
The danger theory: 20 years later
Pradeu, T., & Cooper, E. L. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00287 · Cited by 269
IL ‐33: biological properties, functions, and roles in airway disease
Drake, L. Y., & Kita, H. (2017) · Immunological Reviews · doi:10.1111/imr.12552 · Cited by 258
Shichita, T., Ito, M., Morita, R., Komai, K., Noguchi, Y., Ooboshi, H., Koshida, R., Takahashi, S., Kodama, T., & Yoshimura, A. (2017) · Nature Medicine · doi:10.1038/nm.4312 · Cited by 253
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Siouti, E., & Andreakos, E. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.03.029 · Cited by 255
Kolattukudy, P. E., & Niu, J. (2012) · Circulation Research · doi:10.1161/circresaha.111.243212 · Cited by 249
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Jacobs, A. H., Tavitian, B., & the INMiND consortium (2012) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.53 · Cited by 245
Defining macrophage phenotype and function in adipose tissue
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The S100B protein in biological fluids: more than a lifelong biomarker of brain distress
Michetti, F., Corvino, V., Geloso, M. C., Lattanzi, W., Bernardini, C., Serpero, L. D., & Gazzolo, D. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07612.x · Cited by 242
Trial watch: FDA-approved Toll-like receptor agonists for cancer therapy
Vacchelli, E., Galluzzi, L., Eggermont, A. M. M., Fridman, W. H., Galon, J., Sautès‐Fridman, C., Tartour, É., Zitvogel, L., & Kroemer, G. (2012) · OncoImmunology · doi:10.4161/onci.20931 · Cited by 242
Guo, Q., Zhao, Y., Li, J., Liu, J., Yang, X., Guo, X., Kuang, M., Xia, H., Zhang, Z., Cao, L., et al. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.12.016 · Cited by 253
Damage-Associated Molecular Patterns Control Neutrophil Recruitment
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Sheldon, I. M., Cronin, J., & Bromfield, J. J. (2018) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-020518-115227 · Cited by 239
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Nastase, M. V., Young, M. F., & Schaefer, L. (2012) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155412456380 · Cited by 235
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Li, Y., Huang, H., Liu, B., Zhang, Y. L., Pan, X., Yu, X., Shen, Z., & Song, Y. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00650-z · Cited by 238
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Khakpour, S., Wilhelmsen, K., & Hellman, J. (2015) · Innate Immunity · doi:10.1177/1753425915606525 · Cited by 239
Romero, R. J., Miranda, J., Kusanovic, J. P., Chaiworapongsa, T., Chaemsaithong, P., Martinez, A., Gotsch, F., Dong, Z., Ahmed, A. I., Shaman, M., et al. (2015) · Journal of Perinatal Medicine · doi:10.1515/jpm-2014-0249 · Cited by 235
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Smith, M. M., García-Martínez, E., Pitter, M. R., Fucikova, J. P., Špíšek, R., Zitvogel, L., Kroemer, G., & Galluzzi, L. (2018) · OncoImmunology · doi:10.1080/2162402x.2018.1526250 · Cited by 237
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Herre, M., Cedervall, J., Mackman, N., & Olsson, A. (2022) · Physiological Reviews · doi:10.1152/physrev.00062.2021 · Cited by 240
Prockop, D. J. (2013) · Stem Cells · doi:10.1002/stem.1400 · Cited by 230
RAGE in tissue homeostasis, repair and regeneration
Sorci, G., Riuzzi, F., Giambanco, I., & Donato, R. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.10.021 · Cited by 237
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Bauer, M. E., & la Fuente, M. D. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397803-5.00004-6 · Cited by 229
Gut–liver axis, cirrhosis and portal hypertension: the chicken and the egg
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Autoinhibitory regulation of S100A8/S100A9 alarmin activity locally restricts sterile inflammation
Vogl, T., Stratis, A., Wixler, V., Völler, T., Thurainayagam, S., Jorch, S. K., Zenker, S., Dreiling, A., Chakraborty, D., Fröhling, M., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci89867 · Cited by 233
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Gautheron, J., Gores, G. J., & Rodrigues, C. M. P. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.04.001 · Cited by 225
“However, further investigations are needed to identify which specific DAMPs might preferentially activate one lytic RCD or another.”
BackgroundInfluentialRegulation of Bim in Health and Disease
Sionov, R. V., Vlahopoulos, S., & Granot, Z. (2015) · Oncotarget · doi:10.18632/oncotarget.5492 · Cited by 233
Modifiable risk factors in periodontitis: at the intersection of aging and disease
Reynolds, M. A. (2013) · Periodontology 2000 · doi:10.1111/prd.12047 · Cited by 233
NLRP3 tyrosine phosphorylation is controlled by protein tyrosine phosphatase PTPN22
Spalinger, M. R., Kasper, S., Gottier, C., Lang, S., Atrott, K., Vavricka, S. R., Scharl, S., Gutte, P. M., Grütter, M. G., Beer, H., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci83669 · Cited by 236
Erdal, E., Haider, S. A., Rehwinkel, J., Harris, A. L., & McHugh, P. J. (2017) · Genes & Development · doi:10.1101/gad.289769.116 · Cited by 225
Uric Acid Induces Renal Inflammation via Activating Tubular NF-κB Signaling Pathway
Zhou, Y., Fang, L., Jiang, L., Wen, P., Cao, H., He, W., Dai, C., & Yang, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039738 · Cited by 223
Innate and adaptive immune responses to cell death
Rock, K. L., Lai, J., & Kono, H. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01040.x · Cited by 226
The double-edged functions of necroptosis
Ye, K., Chen, Z., & Xu, Y. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05691-6 · Cited by 239
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Therapeutic Targeting of the Complement System: From Rare Diseases to Pandemics
Garred, P., Tenner, A. J., & Mollnes, T. E. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000072 · Cited by 219
Metadata
- Authors
- Chen, G. Y., & Nuñez, G.
- Affiliations
- University of Michigan (US)
- ORCID
- Chen, Grace Y.
- Venue
- Nature Reviews Immunology
- Published
- 2010-11-19
- Volume
- 10
- Issue
- 12
- Pages
- 826-837
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC3114424
- OpenAlex
- W2042851093
- Semantic Scholar
- ecc0e7ccec243d3412e5a1ad96c82cf4b1c3a3df
- Cited by
- 3,051
- References
- 128
- Citations by year
- 2026: 150 · 2025: 141 · 2024: 186 · 2023: 199 · 2022: 224 · 2021: 245 · 2020: 248 · 2019: 190 · 2018: 231 · 2017: 209 · 2016: 198 · 2015: 193 · 2014: 207 · 2013: 164 · 2012: 148
- FWCI
- 10.93
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Amgen
- National Cancer Institute (CA133185, K08CA133185)
- National Institute of Allergy and Infectious Diseases (R01AI063331, AI06331)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 61707, DK091191, R01DK061707, R01DK091191)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR 051790, R01AR059688, AR059688)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Inflammation biomarkers and pathways
- Keywords
- sterile inflammation, damage-associated molecular patterns, pattern recognition receptors, pathogen-associated molecular patterns, innate immune response, inflammation resolution, inflammatory diseases
- MeSH terms
- Animals, Diabetes Mellitus, Type 2, Humans, Immunity, Innate, Inflammation, Signal Transduction, Reperfusion Injury, Cytokines, Reactive Oxygen Species, Inflammation Mediators, Receptors, Pattern Recognition, Mice
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