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Sensing pathogens and danger signals by the inflammasome
Open accessAbstract
The NLR (nucleotide-binding domain leucine-rich repeat containing) family of intracellular sensors is a crucial component of the innate immune system. A number of NLR family members can form multiprotein complexes, called inflammasomes, and are capable of activating the cysteine protease caspase-1 in response to a wide range of stimuli including both microbial and self-molecules. Caspase-1 activation leads to processing and secretion of the proinflammatory cytokines interleukin-1beta (IL-1beta) and IL-18, which play crucial roles in host defense to infectious insults. Dysregulation of the inflammasome has also been linked to a number of autoinflammatory and autoimmune disorders. Recent advances in the inflammasome field will be discussed in this review.
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“Proinflammatory danger signals induce activity of a multiprotein complex called the Nod-like receptor protein (NLRP)-3 inflammasome (16–18).”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [18]
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“During inflammasome activation, the proform of caspase-1 is recruited to the NLRP-3 complex and cleaved to produce active caspase-1, which then cleaves and activates the potent proinflammatory cytokines IL-1β and IL-18.”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [18]
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Martinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066
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
Cryopyrin activates the inflammasome in response to toxins and ATP
Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080
Hornung, V., Bauernfeind, F., Halle, A., Samstad, E. O., Kono, H., Rock, K. L., Fitzgerald, K. A., & Latz, E. (2008) · Nature Immunology · doi:10.1038/ni.1631 · Cited by 3,065
Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica
Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658
The NALP3 inflammasome is involved in the innate immune response to amyloid-β
Halle, A., Hornung, V., Petzold, G. C., Stewart, C. R., Monks, B. G., Reinheckel, T., Fitzgerald, K. A., Latz, E., Moore, K. J., & Golenbock, D. T. (2008) · Nature Immunology · doi:10.1038/ni.1636 · Cited by 2,441
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
How dying cells alert the immune system to danger
Kono, H., & Rock, K. L. (2008) · Nature Reviews Immunology · doi:10.1038/nri2215 · Cited by 1,737
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
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野口, 武., Sado, T., Naruse, K., Shigetomi, H., Onogi, A., Haruta, S., Kawaguchi, R., Nagai, A., Tanase, Y., Yoshida, S., et al. (2010) · Mediators of Inflammation · doi:10.1155/2010/490406 · Cited by 48
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Galbiati, V., Papale, A., Galli, C. L., Marinovich, M., & Corsini, E. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.203 · Cited by 49
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Biswas, R., Trout, K. L., Jessop, F., Harkema, J. R., & Holian, A. (2017) · Particle and Fibre Toxicology · doi:10.1186/s12989-017-0217-1 · Cited by 46
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Román-Malo, L., & Bullón, P. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071438 · Cited by 41
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Interaction with Sug1 enables Ipaf ubiquitination leading to caspase 8 activation and cell death
Kumar, Y., Radha, V., & Swarup, G. (2010) · Biochemical Journal · doi:10.1042/bj20091349 · Cited by 42
Zhu, Q., Li, X.-X., Wang, W., Hu, J., Li, P., Conley, S. M., & Li, N. (2016) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00344.2015 · Cited by 40
Extracellular ADP facilitates monocyte recruitment in bacterial infection via ERK signaling
Zhang, X., Qin, J., Zou, J., Lv, Z., Tan, B., Shi, J., Zhao, Y., Ren, H., Liu, M., Qian, M., et al. (2016) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.56 · Cited by 39
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Li, L., Shi, C., Dong, F., Xu, G., Lei, M., & Zhang, F. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112168 · Cited by 38
Spooner, R., & Yilmaz, Ö. (2011) · Microbes and Infection · doi:10.1016/j.micinf.2011.10.002 · Cited by 37
In vivoevidence of inflammasome activation during spontaneous labor at term
Panaitescu, B., Romero, R. J., Gomez‐Lopez, N., Xu, Y., Leng, Y., Maymon, E., Pacora, P., Erez, O., Yeo, L., Hassan, S. S., et al. (2018) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2017.1422714 · Cited by 36
Dupont, N., Temime‐Smaali, N., & Lafont, F. (2010) · Biology of the Cell · doi:10.1042/bc20100101 · Cited by 38
Wong, C. K., Leung, T. F., Chu, I. M., Dong, J., Lam, Y. Y. O., & Lam, C. W. K. (2014) · Inflammation · doi:10.1007/s10753-014-0038-4 · Cited by 36
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Lian, H., Fang, X., Li, Q., Liu, S., Wei, Q., Hua, X., Li, W., Liao, C., & Yuan, X. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.845129 · Cited by 34
Plant-derived polysaccharides activate dendritic cell-based anti-cancer immunity
Kikete, S., Luo, L., Jia, B., Wang, L., Ondieki, G., & Bian, Y. (2018) · Cytotechnology · doi:10.1007/s10616-018-0202-z · Cited by 32
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Paoletti, A., Raza, S. Q., Voisin, L., Law, F., da Fonseca, J. P., Caillet, M., Kroemer, G., & Perfettini, J. (2012) · Microbes and Infection · doi:10.1016/j.micinf.2012.05.010 · Cited by 31
Temmoku, J., Fujita, Y., Matsuoka, N., Urano, T., Furuya, M. Y., Asano, T., Sato, S., Matsumoto, H., Watanabe, H., Kozuru, H., et al. (2020) · Modern Rheumatology · doi:10.1080/14397595.2020.1740410 · Cited by 30
Collagen XVII ( BP 180) modulates keratinocyte expression of the proinflammatory chemokine, IL ‐8
den Bergh, F. V., Eliason, S. L., Burmeister, B. T., & Giudice, G. J. (2012) · Experimental Dermatology · doi:10.1111/j.1600-0625.2012.01529.x · Cited by 30
Liarte, S., Chaves-Pozo, E., Abellán, E., Meseguer, J., Mulero, V., Canário, A. V. M., & Ayala, A. G. (2011) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2011.03.015 · Cited by 29
Weatherly, L. M., Shane, H. L., Friend, S. A., Lukomska, E., Baur, R., & Anderson, S. E. (2020) · Toxicological Sciences · doi:10.1093/toxsci/kfaa056 · Cited by 27
Li, S., Chen, X., Peng, W., Hao, G., Geng, X., Zhan, W., & Sun, J. (2016) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2016.04.022 · Cited by 28
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Morimoto, N., Okamura, Y., Maekawa, S., Wang, H., Aoki, T., Kono, T., Sakai, M., & Hikima, J.-I. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.07.027 · Cited by 27
Wang, Y., Pei, S., Liu, Z., Ding, Y., Qian, T., Wen, H., Hsu, S., Zhou, Z., Zhang, J., & Wang, H. (2022) · Cell Death and Disease · doi:10.1038/s41419-023-05621-6 · Cited by 29
JAK inhibitors impair GM-CSF-mediated signaling in innate immune cells
Fujita, Y., Matsuoka, N., Temmoku, J., Furuya-Yashiro, M., Asano, T., Sato, S., Matsumoto, H., Watanabe, H., Kozuru, H., Yatsuhashi, H., et al. (2020) · BMC Immunology · doi:10.1186/s12865-020-00365-w · Cited by 27
Gasparoto, T. H., de Oliveira, C. E., de Freitas, L. T., Pinheiro, C. R., Hori, J. I., Garlet, G. P., Cavassani, K. A., Schillaci, R., Silva, J. S., Zamboni, D. S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107170 · Cited by 28
Pietras, E. M., Miller, L. S., Johnson, C. T., O’Connell, R. M., Dempsey, P. W., & Cheng, G. (2011) · Cell Research · doi:10.1038/cr.2011.59 · Cited by 26
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SYK kinase signaling and the NLRP3 inflammasome in antifungal immunity
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Hydroxychloroquine inhibits IL-1β production from amyloid-stimulated human neutrophils
Fujita, Y., Matsuoka, N., Temmoku, J., Furuya, M. Y., Asano, T., Sato, S., Kobayashi, H., Watanabe, H., Suzuki, E., Urano, T., et al. (2019) · Arthritis Research & Therapy · doi:10.1186/s13075-019-2040-6 · Cited by 24
Li, H., Zhou, X., & Zhang, J. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1865 · Cited by 23
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Zhang, Z., He, L., Hu, S., Wang, Y., Lai, Q., Yang, P. C., Yu, Q., Zhang, S., Xiong, F., Simsekyilmaz, S., et al. (2015) · Europe PMC (PubMed Central) · Cited by 22
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Huang, C. G., Zhou, Y., Cheng, J., Xue, G., Shou, D., Quan, Y., Chen, H., Chen, H., & Zhou, Y. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1145392 · Cited by 21
Rao, J., Elliott, M. R., Leitinger, N., Jensen, R. V., Goldberg, J. B., & Amin, A. R. (2011) · Cellular Immunology · doi:10.1016/j.cellimm.2011.05.012 · Cited by 19
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Fikes, J. D., Patrick, D. J., Francke, S., Frazier, K. S., Reindel, J. F., Romeike, A., Spaet, R. H., Tomlinson, L., & Schafer, K. A. (2015) · Toxicologic Pathology · doi:10.1177/0192623315596382 · Cited by 19
Pazoki, H., Rahimi, H. M., Mirjalali, H., Niyyati, M., Mosaffa, N., Tabaei, S. J. S., Shahrokh, S., Aghdaei, H. A., & Zali, M. R. (2021) · Microbial Pathogenesis · doi:10.1016/j.micpath.2021.105072 · Cited by 18
Scheithauer, L., Thiem, S., Ünal, C., Dellmann, A., & Steinert, M. (2022) · Biomolecules · doi:10.3390/biom12050624 · Cited by 18
Yokota, S., Kikuchi, M., Nozawa, T., Kanetaka, T., Sato, T., Yamazaki, K., Sakurai, N., Hara, R., & Mori, M. (2014) · Modern Rheumatology · doi:10.3109/14397595.2014.902747 · Cited by 18
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Shane, H. L., Long, C. M., & Anderson, S. E. (2019) · Journal of Immunotoxicology · doi:10.1080/1547691x.2018.1515279 · Cited by 18
Kitade, T., Horiki, N., Katsurahara, M., Totoki, T., Harada, T., Tano, S., Yamada, R., Hamada, Y., Inoue, H., Tanaka, K., et al. (2015) · Internal Medicine · doi:10.2169/internalmedicine.54.3690 · Cited by 17
Li, T., Huang, C., Yang, Y., Lee, K., Hsieh, S.-L., Hsieh, Y., Alan, L., Lin, H., Lee, S., & Tsai, C. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147212 · Cited by 16
Piotrowska, K., Zgutka, K., Tkacz, M., & Tarnowski, M. (2023) · Antioxidants · doi:10.3390/antiox12081488 · Cited by 18
Dey-Rao, R., & Sinha, A. A. (2015) · Genes and Immunity · doi:10.1038/gene.2015.48 · Cited by 15
Morimoto, N., Okamura, Y., Kono, T., Sakai, M., & Hikima, J.-I. (2020) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2020.103894 · Cited by 15
Cold-inducible RNA-binding protein (CIRP) potentiates uric acid-induced IL-1β production
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Cheng, C., Lee, Y.-S., Chang, C., Lin, J., & Lin, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140128 · Cited by 15
Ulland, T. K., Janowski, A. M., Buchan, B. W., Faron, M. L., Cassel, S. L., Jones, B. D., & Sutterwala, F. S. (2012) · Infection and Immunity · doi:10.1128/iai.00991-12 · Cited by 14
VEGF-like protein from Apostichopus japonicus promotes cell proliferation and migration
Lv, Z., Guo, M. Z., Li, C., Shao, Y., Zhao, X., & Zhang, W. (2018) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2018.11.017 · Cited by 13
Gevokizumab in type 1 diabetes mellitus: extreme remedies for extreme diseases?
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Rôle de l’inflammasome dans les pathologies cardiovasculaires
Connat, J.-L. (2011) · Annales de Cardiologie et d'Angéiologie · doi:10.1016/j.ancard.2010.07.011 · Cited by 12
Li, H., Sun, L., & Wang, Y. (2023) · Molecular Medicine Reports · doi:10.3892/mmr.2023.12993 · Cited by 12
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Snyder, P. W. (2012) · Toxicologic Pathology · doi:10.1177/0192623311431468 · Cited by 10
Lung Aspergillosis in renal cell carcinoma patient treated with sunitinib
Visvardis, E., Gao, F., Paes, M. N., Duprez, O., & Waxman, J. (2011) · QJM · doi:10.1093/qjmed/hcr091 · Cited by 10
Pathogen Strategies to Evade Innate Immune Response: A Signaling Point of View
Miguel, B., Celeste, M. G., & Teresa, M. (2012) · InTech eBooks · doi:10.5772/37771 · Cited by 14
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Ranson, N., & Eri, R. D. (2013) · American journal of medical and biological research · doi:10.12691/ajmbr-1-3-3 · Cited by 9
L’inflammasome NLRP3 : physiopathologie et application thérapeutique
Gicquel, T., Robert, S., Victoni, T., & Lagente, V. (2016) · La Presse Médicale · doi:10.1016/j.lpm.2016.01.006 · Cited by 12
Potential diabetic cardiomyopathy therapies targeting pyroptosis: A mini review
Yu, J., Li, D., Yu, J. Y., Jiang, W., Liao, X., & Zhao, Q. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.985020 · Cited by 9
Modelling experimental uveitis: barrier effects in autoimmune disease
Nicholson, D., Kerr, E. C., Jepps, O. G., & Nicholson, L. B. (2012) · Inflammation Research · doi:10.1007/s00011-012-0469-z · Cited by 8
Functional capability of IL-15-Akt signaling in the denervated muscle.
Zhao, H., & Huang, H.-W. (2012) · Cytokine · doi:10.1016/j.cyto.2012.08.026 · Cited by 9
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Niller, H. H., & Minárovits, J. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-388415-2.00021-4 · Cited by 7
H3N2 canine influenza virus NS1 protein inhibits canine NLRP3 inflammasome activation
Tao, P., Ning, Z., Zhou, P., Xiao, W., Wang, G., Li, S., & Zhang, G. (2022) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2022.110483 · Cited by 6
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Suresh, R. V., Bradley, E. W., Higgs, M. G., Russo, V. C., Alqahtani, M., Huang, W., Bakshi, C. S., & Malik, M. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.725572 · Cited by 6
Yu, J., Zhu, H., Saeid, T., Lee, J.-Y., Diamond, D. M., Kirstein, C. L., & Kindy, M. S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27052281 · Cited by 5
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Chaskiel, L., Dantzer, R., & Konsman, J. P. (2021) · Pharmaceuticals · doi:10.3390/ph14101030 · Cited by 5
Kim, S. Y., Son, M. K., Park, J. H., Na, H. S., & Chung, J. (2024) · Pathogens · doi:10.3390/pathogens13060474 · Cited by 5
Immunophysiology of the avian immune system
Kogut, M. H. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819770-7.00020-7 · Cited by 6
Nv, K. (2015) · Medical Immunology (Russia) · doi:10.15789/1563-0625-2015-2-109-118 · Cited by 4
Kaarthikeyan, G., Balakrishnan, A., & Jayakumar, N. D. (2018) · Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale · doi:10.4081/jbr.2018.7202 · Cited by 4
Inflammatory Cells of the Lung: Macrophages
Migliaccio, C. T., & Holian, A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-046884-6.00905-2 · Cited by 4
Mandrekar, P., & Szabó, G. (2010) · Molecular pathology library · doi:10.1007/978-1-4419-7107-4_27 · Cited by 3
Exploring Inflammasome Complex as a Therapeutic Approach in Inflammatory Diseases
Sultana, S., Viet, T. D., Oishy, T. A., Kazi, E., Micolucci, L., Mollah, A. K. M. M., Akhtar, M. M., & Islam, M. S. (2023) · Future Pharmacology · doi:10.3390/futurepharmacol3040048 · Cited by 3
Evasion of mammalian defense systems by orthopoxviruses
Shchelkunov, S. N. (2011) · Molecular Biology · doi:10.1134/s0026893311010109 · Cited by 3
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Metadata
- Authors
- Pedra, J. H., Cassel, S. L., & Sutterwala, F. S.
- Affiliations
- University of California, Riverside (US)
- University of Iowa (US)
- Corresponding author
- Pedra, Joao HF
- Sutterwala, Fayyaz S
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 2009-02
- Volume
- 21
- Issue
- 1
- Pages
- 10-16
- ISSN
- 0952-7915 (ISSN-L)
- PMC
- PMC2701640
- OpenAlex
- W2171309698
- Cited by
- 233
- References
- 65
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 4 · 2023: 9 · 2022: 9 · 2021: 7 · 2020: 13 · 2019: 12 · 2018: 13 · 2017: 8 · 2016: 19 · 2015: 11 · 2014: 20 · 2013: 22 · 2012: 29
- FWCI
- 2.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- Centers for Disease Control and Prevention (K01CK000101)
- National Institute of Allergy and Infectious Diseases (K08AI067736, K08AI065517)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Keywords
- inflammasome, caspase-1 activation, IL-1β, IL-18, innate immunity, pathogen recognition, damage-associated molecular patterns, autoinflammatory disease, autoimmune disease, host defense
- MeSH terms
- NLR Proteins, Animals, Autoimmune Diseases, Bacterial Infections, Calcium-Binding Proteins, Gene Expression Regulation, Humans, Immunity, Innate, Polymorphism, Genetic, Signal Transduction, Genetic Predisposition to Disease, Caspase 1, Intercellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, Apoptosis Regulatory Proteins, CARD Signaling Adaptor Proteins, Interleukin-1beta, Host-Pathogen Interactions
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