The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Gout-associated uric acid crystals activate the NALP3 inflammasome
Abstract
Development of the acute and chronic inflammatory responses known as gout and pseudogout are associated with the deposition of monosodium urate (MSU) or calcium pyrophosphate dihydrate (CPPD) crystals, respectively, in joints and periarticular tissues. Although MSU crystals were first identified as the aetiological agent of gout in the eighteenth century and more recently as a 'danger signal' released from dying cells, little is known about the molecular mechanisms underlying MSU- or CPPD-induced inflammation. Here we show that MSU and CPPD engage the caspase-1-activating NALP3 (also called cryopyrin) inflammasome, resulting in the production of active interleukin (IL)-1beta and IL-18. Macrophages from mice deficient in various components of the inflammasome such as caspase-1, ASC and NALP3 are defective in crystal-induced IL-1beta activation. Moreover, an impaired neutrophil influx is found in an in vivo model of crystal-induced peritonitis in inflammasome-deficient mice or mice deficient in the IL-1beta receptor (IL-1R). These findings provide insight into the molecular processes underlying the inflammatory conditions of gout and pseudogout, and further support a pivotal role of the inflammasome in several autoinflammatory diseases.
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In the citing paper
“Colchicine impairs neutrophil adhesion to vascular endothelium and degranulation and blocks activation of the NLRP3 (NOD-, LRR-, and pyrin domaincontaining protein 3) inflammasome, which is required for cleaving caspase-1 leading to the production of IL-1 β and IL-18. 134-136”
From COVID-19, Myocarditis and Pericarditis (2023) · cites this paper as [135]
In the citing paper
“Nucleotide products such as uric acid can also function as DAMPs, presumably by activating the inflammasome in APC, thereby stimulating the production of inflammatory cytokines such as interleukin-1β (IL-1β), IL-18 and IL-33, the secretion of which depends on the inflammasome-mediated activation of caspase-145,46.”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [46]
In the citing paper
“The secretion of mature IL-1β induced by asbestos was comparable to amounts observed with monosodium urate crystals (MSU), a known potent activator of IL-1β processing (7) (Fig. 1, A and B).”
From Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica (2008) · cites this paper as [7]
In the citing paper
“In addition to PAMPs, Nalp3 has the extraordinary capacity of sensing endogenous stress-associated danger signals (DAMPs) such as ATP (9) or MSU (7).”
From Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica (2008) · cites this paper as [7]
In the citing paper
“The Nalp3 inflammasome is implicated in the pathological increase of IL-1β production in autoinflammatory syndromes, such as Muckle-Wells syndrome (22), as well as inflammatory processes, such as gout and pseudogout (7).”
From Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica (2008) · cites this paper as [7]
In the citing paper
“The NLRP3 inflammasome senses crystalline danger signals that can occur during autoinflammatory diseases, such as gout or atherosclerosis, and environmental diseases, such as silicosis or asbestosis (18, 20, 22).”
From Volcanic Ash Activates the NLRP3 Inflammasome in Murine and Human Macrophages (2018) · cites this paper as [18]
In the citing paper
“Inhalation of crystalline silica can induce inflammation by stimulating the NLRP3 inflammasome, a cytosolic receptor complex that plays a critical role in driving inflammatory immune responses.”
From Volcanic Ash Activates the NLRP3 Inflammasome in Murine and Human Macrophages (2018) · cites this paper as [18]
In the citing paper
“NLRP3 has been shown to respond to sterile stimuli, including asbestos, silica, MSU and CPPD crystals55, cholesterol crystals and β-amyloid fibrils56.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [55]
In the citing paper
“Urate and cholesterol crystals, as well as sterile particulates, for example, can bypass the requirement for ATP and P2RX7 for IL-1β production55,59.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [55]
In the citing paper
“Consistently, in mouse models of sterile injury, such as gout, asbestosis and silicosis, NLRP3-deficient mice exhibited decreased inflammation with reduced levels of tissue infiltration by neutrophils or macrophages55,57,58.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [55]
In the citing paper
“The inflammasome is a multimolecular cytosolic sensor that detects pathogenic microorganisms and sterile stressors and activates caspase-1 during the process of pyroptosis, which, in turn, causes the inactive precursor forms of interleukin-1β and interleukin-18 to become the active forms.”
From Cytokine storm (2020) · cites this paper as [41]
Citations
Cites
Janeway, C. A., & Medzhitov, R. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.083001.084359 · Cited by 8,394
Martinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066
Self-citationThe Danger Model: A Renewed Sense of Self
Matzinger, P. (2002) · Science · doi:10.1126/science.1071059 · Cited by 4,205
Differential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf
Mariathasan, S., Newton, K., Monack, D. M., Vucic, D., French, D. M., Lee, W. P., Roose-Girma, M., Erickson, S. L., & Dixit, V. M. (2004) · Nature · doi:10.1038/nature02664 · Cited by 1,864
Agostini, L., Martinon, F., Burns, K., McDermott, M. F., Hawkins, P. N., & Tschopp, J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00046-9 · Cited by 1,768
Self-citationMolecular identification of a danger signal that alerts the immune system to dying cells
Shi, Y., Evans, J. E., & Rock, K. L. (2003) · Nature · doi:10.1038/nature01991 · Cited by 1,684
Hoffman, H. M., Mueller, J. L., Broide, D. H., Wanderer, A. A., & Kolodner, R. D. (2001) · Nature Genetics · doi:10.1038/ng756 · Cited by 1,679
Martinon, F., & Tschopp, J. (2004) · Cell · doi:10.1016/j.cell.2004.05.004 · Cited by 957
Self-citationNALPs: a novel protein family involved in inflammation
Tschopp, J., Martinon, F., & Burns, K. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1019 · Cited by 739
Self-citationNLRs join TLRs as innate sensors of pathogens
Martinon, F., & Tschopp, J. (2005) · Trends in Immunology · doi:10.1016/j.it.2005.06.004 · Cited by 673
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Cipolletta, E., Tata, L. J., Nakafero, G., Avery, A. J., Mamas, M. A., & Abhishek, A. (2022) · JAMA · doi:10.1001/jama.2022.11390 · Cited by 245
Garg, A. D., Dudek-Perić, A. M., Romano, E., & Agostinis, P. (2015) · The International Journal of Developmental Biology · doi:10.1387/ijdb.150061pa · Cited by 250
Ritter, M., Gross, O., Kays, S., Ruland, J., Nimmerjahn, F., Saijo, S., Tschopp, J., Layland, L. E., & Prazeres da Costa, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010337107 · Cited by 243
Self-citationIp, W., & Medzhitov, R. M. (2015) · Nature Communications · doi:10.1038/ncomms7931 · Cited by 251
Is interleukin‐1 a good or bad ‘guy’ in tumor immunobiology and immunotherapy?
Apte, R. N., & Voronov, E. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00615.x · Cited by 243
Duffy, D., Rouilly, V., Libri, V., Hasan, M., Beitz, B., David, M., Urrutia, A., Bisiaux, A., LaBrie, S. T., Dubois, A., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.03.002 · Cited by 242
Lyngdoh, T., Marques-Vidal, P. M., Paccaud, F. M., Preisig, M., Waeber, G., Bochud, M., & Vollenweider, P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019901 · Cited by 242
Schlesinger, N., Mysler, E., Lin, H.-Y., Meulemeester, M. D., Rovenský, J., Arulmani, U., Balfour, A., Krammer, G., Sallstig, P., & So, A. (2011) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2010.144063 · Cited by 245
Cholesterol crystal induced arterial inflammation and destabilization of atherosclerotic plaque
Janoudi, A., Shamoun, F. E., Kalavakunta, J. K., & Abela, G. S. (2015) · European Heart Journal · doi:10.1093/eurheartj/ehv653 · Cited by 243
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Gong, T., Yang, Y., Jin, T., Jiang, W., & Zhou, R. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.01.009 · Cited by 250
Induction of Pyroptosis and Its Implications in Cancer Management
Wang, Y., Liu, X., & Zhao, R. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00971 · Cited by 246
Jin, C., Frayssinet, P., Pelker, R. R., Cwirka, D., Hu, B., Vignery, A., Eisenbarth, S. C., & Flavell, R. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111101108 · Cited by 241
P2X7 receptor and the NLRP3 inflammasome: Partners in crime
Pelegrín, P. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114385 · Cited by 253
Targeting innate immunity-driven inflammation in CKD and cardiovascular disease
Speer, T., Dimmeler, S., Schunk, S. J., Fliser, D., & Ridker, P. M. (2022) · Nature Reviews Nephrology · doi:10.1038/s41581-022-00621-9 · Cited by 251
Øvrevik, J., Refsnes, M., Låg, M., Holme, J. A., & Schwarze, P. E. (2015) · Biomolecules · doi:10.3390/biom5031399 · Cited by 247
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Desai, J., Steiger, S., & Anders, H. (2017) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2017.06.005 · Cited by 246
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Xu, J., Jiang, Y., Wang, J., Shi, X., Liu, Q., Liu, Z., Li, Y., Scott, M. J., Xiao, G., Li, S., et al. (2014) · Cell Death & Differentiation · doi:10.1038/cdd.2014.40 · Cited by 239
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Wang, W., Wang, X., Chun, J., Vilaysane, A., Clark, S. A., French, G., Bracey, N. A., Trpkov, K., Bonni, S., Duff, H. J., et al. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201959 · Cited by 239
Man, S. M., Tourlomousis, P., Hopkins, L., Monie, T. P., Fitzgerald, K. A., & Bryant, C. E. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301581 · Cited by 239
Cremer, P. C., Kumar, A., Kontzias, A., Tan, C. D., Rodríguez, E. R., Imazio, M., & Klein, A. L. (2016) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2016.07.785 · Cited by 239
Regulation of NLRP3 Inflammasome by Phosphorylation
Song, N., & Li, T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02305 · Cited by 239
Wang, W., Hu, D., Feng, Y., Wu, J., Li, A., Wang, Y., Cheng, K., Tian, M., Xiao, F., Zhang, Q., et al. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008335 · Cited by 240
Zhang, M., Zhang, X., Tian, T., Zhang, Q., Wen, Y., Zhu, J., Xiao, D., Cui, W., & Lin, Y. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.06.003 · Cited by 240
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Kistowska, M., Gehrke, S., Jankovic, D. L., Kerl, K., Fettelschoss‐Gabriel, A., Feldmeyer, L., Fenini, G., Kolios, A. G. A., Navarini, A. A., Gancevičienė, R., et al. (2013) · Journal of Investigative Dermatology · doi:10.1038/jid.2013.438 · Cited by 239
Gout therapeutics: new drugs for an old disease
Burns, C. M., & Wortmann, R. L. (2010) · The Lancet · doi:10.1016/s0140-6736(10)60665-4 · Cited by 238
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Jankovic, D. L., Ganesan, J., Bscheider, M., Stickel, N., Weber, F. C., Guarda, G., Follo, M., Pfeifer, D., Tardivel, A., Ludigs, K., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20130084 · Cited by 241
Self-citationZhong, F. L., Robinson, K. S., Teo, D. E. T., Tan, K. Y., Lim, C., Harapas, C. R., Yu, C., Xie, W. H., Sobota, R. M., Au, B. V., et al. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.004350 · Cited by 246
Pathogen recognition by innate receptors
Kumagai, Y., Takeuchi, O., & Akira, S. (2008) · Journal of Infection and Chemotherapy · doi:10.1007/s10156-008-0596-1 · Cited by 241
Harder, J., Franchi, L., Muñoz-Planillo, R., Park, J., Reimer, T., & Núñez, G. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900444 · Cited by 239
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Sánchez‐López, E., Zhong, Z., Stubelius, A., Sweeney, S., Booshehri, L. M., Antonucci, L., Liu‐Bryan, R., Lodi, A., Terkeltaub, R. A., Lacal, J. C., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.03.011 · Cited by 240
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Cullen, S. P., Kearney, C. J., Clancy, D. M., & Martin, S. J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.003 · Cited by 234
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Franchi, L., Park, J., Shaw, M. H., Marina–García, N., Chen, G., Kim, Y.-G., & Núñez, G. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.01059.x · Cited by 235
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Kahrilas, P. J., & Boeckxstaens, G. E. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.08.038 · Cited by 236
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Chiaro, T. R., Soto, R., Stephens, W. Z., Kubinak, J. L., Petersen, C., Gogokhia, L., Bell, R. S., Delgado, J. C., Cox, J. E., Voth, W. P., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf9044 · Cited by 237
Vince, J. E., Nardo, D. D., Gao, W., Vince, A. J., Hall, C. M., McArthur, K., Simpson, D. S., Vijayaraj, S. L., Lindqvist, L., Bouillet, P., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.103 · Cited by 236
Inflammasome-mediated regulation of hepatic stellate cells
Watanabe, A., Sohail, M. A., Gomes, D. A., Hashmi, A., Nagata, J., Sutterwala, F. S., Mahmood, S., Jhandier, M. N., Shi, Y., Flavell, R. A., et al. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90223.2008 · Cited by 233
Sensing pathogens and danger signals by the inflammasome
Pedra, J. H., Cassel, S. L., & Sutterwala, F. S. (2009) · Current Opinion in Immunology · doi:10.1016/j.coi.2009.01.006 · Cited by 233
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Geddes, K., Magalhaes, J. G., & Girardin, S. E. (2009) · Nature Reviews Drug Discovery · doi:10.1038/nrd2783 · Cited by 242
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Shaw, P. J., McDermott, M., & Kanneganti, T. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.11.001 · Cited by 240
Bosch, T. C. G., Augustin, R., Anton‐Erxleben, F., Fraune, S., Hemmrich, G., Zill, H., Rosenstiel, P. C., Jacobs, G., Schreiber, S., Leippe, M., et al. (2008) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2008.10.004 · Cited by 233
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Doherty, M. (2009) · Rheumatology · doi:10.1093/rheumatology/kep086 · Cited by 233
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Apel, F., Zychlinsky, A., & Kenny, E. F. (2018) · Nature Reviews Rheumatology · doi:10.1038/s41584-018-0039-z · Cited by 233
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Barry, R. E., John, S. W., Liccardi, G., Tenev, T., Jaco, I., Chen, C., Choi, J. C.-B., Kasperkiewicz, P., Fernandes‐Alnemri, T., Alnemri, E. S., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05321-2 · Cited by 240
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Noonin, C., & Thongboonkerd, V. (2021) · Theranostics · doi:10.7150/thno.54004 · Cited by 234
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Kasahara, K., Kerby, R. L., Zhang, Q., Pradhan, M., Mehrabian, M., Lusis, A. J., Bergström, G. M. L., Bäckhed, F., & Rey, F. E. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.05.011 · Cited by 237
Natsuaki, Y., Egawa, G., Nakamizo, S., Ono, S., Hanakawa, S., Okada, T., Kusuba, N., Otsuka, A., Kitoh, A., Honda, T., et al. (2014) · Nature Immunology · doi:10.1038/ni.2992 · Cited by 232
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Hutton, H., Ooi, J. D., Holdsworth, S. R., & Kitching, A. R. (2016) · Nephrology · doi:10.1111/nep.12785 · Cited by 237
Nakamura, K., Kassem, S., Cleynen, A., Chrétien, M., Guillerey, C., Putz, E. M., Bald, T., Förster, I., Vučković, S., Hill, G. R., et al. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.02.007 · Cited by 239
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Mulay, S. R., Linkermann, A., & Anders, H. (2015) · Journal of the American Society of Nephrology · doi:10.1681/asn.2015040405 · Cited by 233
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Knauf, F., Asplin, J. R., Granja, I., Schmidt, I. M., Moeckel, G. W., David, R. J., Flavell, R. A., & Aronson, P. S. (2013) · Kidney International · doi:10.1038/ki.2013.207 · Cited by 231
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Bono, J. S. D., Guo, C. W., Gürel, B., Marzo, A. M. D., Sfanos, K. S., Mani, R. S., Gil, J., Drake, C. G., & Alimonti, A. (2020) · Nature reviews. Cancer · doi:10.1038/s41568-020-0267-9 · Cited by 240
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Haneklaus, M., O'Neill, L. A. J., & Coll, R. C. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2012.12.004 · Cited by 230
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Higashikuni, Y., Liu, W., Numata, G., Tanaka, K., Fukuda, D., Tanaka, Y., Hirata, Y., Imamura, T., Takimoto, E., Komuro, I., et al. (2022) · Circulation · doi:10.1161/circulationaha.122.060860 · Cited by 234
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Richette, P., Pérez-Ruiz, F., Doherty, M., Jansen, T., Nuki, G., Pascual, E., Punzi, L., So, A. K.-L., & Bardin, T. (2014) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2014.124 · Cited by 228
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Walsh, J. G., Reinke, S. N., Mamik, M. K., McKenzie, B., Maingat, F. G., Branton, W. G., Broadhurst, D., & Power, C. (2014) · Retrovirology · doi:10.1186/1742-4690-11-35 · Cited by 236
Grayson, P. C., & Kaplan, M. J. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.5bt0615-247r · Cited by 234
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Hamarsheh, S., & Zeiser, R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01444 · Cited by 233
NLR proteins: integral members of innate immunity and mediators of inflammatory diseases
Wilmanski, J., Petnicki‐Ocwieja, T., & Kobayashi, K. S. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0607402 · Cited by 237
Anders, H., Suárez-Álvarez, B., Grigorescu, M., Foresto‐Neto, O., Steiger, S., Desai, J., Marschner, J. A., Honarpisheh, M. M., Shi, C., Jordan, J., et al. (2017) · Kidney International · doi:10.1016/j.kint.2017.09.022 · Cited by 226
Danger signalling during cancer cell death: origins, plasticity and regulation
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Guigoz, Y., Dore, J. M., & Schiffrin, E. J. (2008) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e3282f2bfdf · Cited by 230
How Metabolism Generates Signals during Innate Immunity and Inflammation
McGettrick, A. F., & O'Neill, L. A. J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.r113.486464 · Cited by 232
Deo, P., Chow, S. H., Han, M., Speir, M., Huang, C., Schittenhelm, R. B., Dhital, S., Emery, J., Li, J., Kile, B. T., et al. (2020) · Nature Microbiology · doi:10.1038/s41564-020-0773-2 · Cited by 225
Macia, L., Thorburn, A. N., Binge, L. C., Mariño, E., Rogers, K. E., Maslowski, K. M., Vieira, A. T., Kranich, J., & Mackay, C. R. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01080.x · Cited by 227
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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
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Yu, H. B., & Finlay, B. B. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.08.007 · Cited by 229
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Mulay, S. R., & Anders, H. (2017) · Nature Reviews Nephrology · doi:10.1038/nrneph.2017.10 · Cited by 227
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McDermott, M., Kingsbury, S. R., & Conaghan, P. G. (2011) · Journal of Inflammation Research · doi:10.2147/jir.s11330 · Cited by 225
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Rock, K. L., Lai, J., & Kono, H. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01040.x · Cited by 226
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Self-citationChang, Y.-P., Ka, S., Hsu, W., Chen, A., Chao, L. K., Lin, C.-C., Hsieh, C.-C., Chen, M., Chiu, H.-W., Ho, C., et al. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24903 · Cited by 220
Sibley, C. H., Plass, N., Snow, J., Wiggs, E. A., Brewer, C. C., King, K. A., Zalewski, C. K., Kim, H. J., Bishop, R. J., Hill, S. C., et al. (2012) · Arthritis & Rheumatism · doi:10.1002/art.34409 · Cited by 221
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Honda, H., Nagai, Y., Matsunaga, T., Okamoto, N., Watanabe, Y., Tsuneyama, K., Hayashi, H., Fujii, I., Ikutani, M., Hirai, Y., et al. (2014) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a0114-005rr · Cited by 215
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Zhao, Y., & Shao, F. (2015) · Immunological Reviews · doi:10.1111/imr.12293 · Cited by 224
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Rimessi, A., Previati, M., Nigro, F., Wieckowski, M. R., & Pinton, P. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.06.015 · Cited by 216
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Metadata
- Authors
- Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J.
- Affiliations
- University of Lausanne (CH)
- Corresponding author
- Tschopp, Jürg
- Venue
- Nature
- Published
- 2006-01-11
- Volume
- 440
- Issue
- 7081
- Pages
- 237-241
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2009800174
- Cited by
- 5,326
- References
- 31
- Citations by year
- 2026: 227 · 2025: 246 · 2024: 305 · 2023: 310 · 2022: 333 · 2021: 335 · 2020: 340 · 2019: 297 · 2018: 280 · 2017: 248 · 2016: 287 · 2015: 290 · 2014: 271 · 2013: 299 · 2012: 238
- FWCI
- 76.62
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Health Sciences › Medicine › Nephrology › Gout, Hyperuricemia, Uric Acid
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- NLRP3 inflammasome, NLRP3, gout, urate crystals, monosodium urate, calcium pyrophosphate dihydrate, pseudogout, caspase-1, IL-1β, IL-18, autoinflammatory disease, innate immunity, crystal-induced inflammation, neutrophil influx, IL-1 receptor, macrophages
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Calcium Pyrophosphate, Carrier Proteins, Cell Line, Cells, Cultured, Chondrocalcinosis, Colchicine, Disease Models, Animal, Gout, Humans, Inflammation, Interleukin-1, Macrophages, Neutrophils, Peritonitis, Uric Acid, Receptors, Interleukin-1, Caspase 1, Mice
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