The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
AIM2 recognizes cytosolic dsDNA and forms a caspase-1-activating inflammasome with ASC
Open accessAbstract
The innate immune system senses nucleic acids by germline-encoded pattern recognition receptors. RNA is sensed by Toll-like receptor members TLR3, TLR7 and TLR8, or by the RNA helicases RIG-I (also known as DDX58) and MDA-5 (IFIH1). Little is known about sensors for cytoplasmic DNA that trigger antiviral and/or inflammatory responses. The best characterized of these responses involves activation of the TANK-binding kinase (TBK1)-interferon regulatory factor 3 (IRF3) signalling axis to trigger transcriptional induction of type I interferon genes. A second, less well-defined pathway leads to the activation of an 'inflammasome' that, via caspase-1, controls the catalytic cleavage of the pro-forms of the cytokines IL1beta and IL18 (refs 6, 7). Using mouse and human cells, here we identify the PYHIN (pyrin and HIN domain-containing protein) family member absent in melanoma 2 (AIM2) as a receptor for cytosolic DNA, which regulates caspase-1. The HIN200 domain of AIM2 binds to DNA, whereas the pyrin domain (but not that of the other PYHIN family members) associates with the adaptor molecule ASC (apoptosis-associated speck-like protein containing a caspase activation and recruitment domain) to activate both NF-kappaB and caspase-1. Knockdown of Aim2 abrogates caspase-1 activation in response to cytoplasmic double-stranded DNA and the double-stranded DNA vaccinia virus. Collectively, these observations identify AIM2 as a new receptor for cytoplasmic DNA, which forms an inflammasome with the ligand and ASC to activate caspase-1.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“Although distinct from NLRs, AIM2 has a pyrin domain that allows it to interact with the adaptor protein ASC (apoptosis-associated speck-like protein containing a CARD) to form the inflammasome50.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [50]
In the citing paper
“The AIM2 inflammasome has been recently shown to recognize cytoplasmic double-stranded DNA (dsDNA) that is not necessarily microbial in origin, resulting in caspase 1 activation and IL-1β secretion48–50.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [50]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
MUSCLE: multiple sequence alignment with high accuracy and high throughput
Edgar, R. C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh340 · Cited by 44,662
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
Self-citationDAI (DLM-1/ZBP1) is a cytosolic DNA sensor and an activator of innate immune response
Takaoka, A., Wang, Z., Choi, M. K., Yanai, H., Negishi, H., Ban, T., Lu, Y., Miyagishi, M., Kodama, T., Honda, K., et al. (2007) · Nature · doi:10.1038/nature06013 · Cited by 1,704
Intracellular pattern recognition receptors in the host response
Meylan, E., Tschopp, J., & Karin, M. (2006) · Nature · doi:10.1038/nature04946 · Cited by 1,196
Recognition of Cytosolic DNA Activates an IRF3-Dependent Innate Immune Response
Stetson, D. B., & Medzhitov, R. M. (2006) · Immunity · doi:10.1016/j.immuni.2005.12.003 · Cited by 1,003
The inflammasome recognizes cytosolic microbial and host DNA and triggers an innate immune response
Muruve, D. A., Pétrilli, V., Zaiss, A. K., White, L. R., Clark, S. A., Ross, P. J., Parks, R. J., & Tschopp, J. (2008) · Nature · doi:10.1038/nature06664 · Cited by 965
A Toll-like receptor–independent antiviral response induced by double-stranded B-form DNA
Ishii, K. J., Coban, C., Kato, H., Takahashi, K., Torii, Y., Takeshita, F., Ludwig, H., Sutter, G., Suzuki, K., Hemmi, H., et al. (2005) · Nature Immunology · doi:10.1038/ni1282 · Cited by 771
Enzymatic Synthesis of Deoxyribonucleic Acid
Richardson, C. C., Schildkraut, C. L., Aposhian, H. V., & Kornberg, A. (1964) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)51772-5 · Cited by 718
Kanneganti, T., Body–Malapel, M., Amer, A. O., Park, J., Whitfield, J. R., Franchi, L., Taraporewala, Z. F., Miller, D. J., Patton, J. T., Inohara, N., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607594200 · Cited by 706
TANK-binding kinase-1 delineates innate and adaptive immune responses to DNA vaccines
Ishii, K. J., Kawagoe, T., Koyama, S., Matsui, K., Kumar, H., Kawai, T., Uematsu, S., Takeuchi, O., Takeshita, F., Coban, C., et al. (2008) · Nature · doi:10.1038/nature06537 · Cited by 633
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 1,004
Role of AIM2 inflammasome in inflammatory diseases, cancer and infection
Sharma, B. R., Karki, R., & Kanneganti, T. (2019) · European Journal of Immunology · doi:10.1002/eji.201848070 · Cited by 301
Inflammasomes in cancer: a double-edged sword
Kolb, R. H., Liu, G., Janowski, A. M., Sutterwala, F. S., & Zhang, W. (2013) · Protein & Cell · doi:10.1007/s13238-013-0001-4 · Cited by 300
Inflammasome-independent role of AIM2 in suppressing colon tumorigenesis via DNA-PK and Akt
Wilson, J. E., Petrucelli, A., Chen, L., Koblansky, A. A., Truax, A. D., Oyama, Y., Rogers, A. B., Brickey, W. J., Wang, Y., Schneider, M., et al. (2015) · Nature Medicine · doi:10.1038/nm.3908 · Cited by 303
STOJANOV, S., Lapidus, S., Chitkara, P., Feder, H. M., Salazar, J. C., Fleisher, T. A., Brown, M. R., Edwards, K. M., Ward, M. M., Colbert, R. A., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103681108 · Cited by 293
Pandey, A. K., Yang, Y., Jiang, Z., Fortune, S. M., Coulombe, F., Behr, M. A., Fitzgerald, K. A., Sassetti, C. M., & Kelliher, M. A. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000500 · Cited by 292
Self-citationWu, J., Fernandes‐Alnemri, T., & Alnemri, E. S. (2010) · Journal of Clinical Immunology · doi:10.1007/s10875-010-9425-2 · Cited by 300
PANoptosis: A Unique Innate Immune Inflammatory Cell Death Modality
Nagakannan, P., & Kanneganti, T. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2200508 · Cited by 306
Which cell death modality wins the contest for photodynamic therapy of cancer?
Mishchenko, T. A., Balalaeva, I. V., Gorokhova, A. A., Vedunova, M. V., & Krysko, D. V. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04851-4 · Cited by 293
Aicardi-Goutieres syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity
Crow, Y. J., & Rehwinkel, J. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp293 · Cited by 289
Bossaller, L., Chiang, P.-I., Schmidt‐Lauber, C., Ganesan, S., Kaiser, W. J., Rathinam, V. A. K., Mocarski, E. S., Subramanian, D., Green, D. R., Silverman, N. S., et al. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1202121 · Cited by 287
Self-citationBeyond pattern recognition: five immune checkpoints for scaling the microbial threat
Blander, J. M., & Sander, L. E. (2012) · Nature reviews. Immunology · doi:10.1038/nri3167 · Cited by 300
Hartmann, G. (2017) · Advances in Immunology · doi:10.1016/bs.ai.2016.11.001 · Cited by 285
IRAK-1 bypasses priming and directly links TLRs to rapid NLRP3 inflammasome activation
Lin, K.-M., Hu, W., Troutman, T. D., Jennings, M., Brewer, T., Li, X., Nanda, S. K., Cohen, P., Thomas, J. A., & Pasare, C. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320294111 · Cited by 285
Ichinohe, T., Yamazaki, T., Koshiba, T., & Yanagi, Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312571110 · Cited by 291
Beckwith, K. S., Beckwith, M. S., Ullmann, S., Sætra, R. S., Kim, H., Marstad, A., Åsberg, S. E., Strand, T. A., Haug, M., Niederweis, M., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16143-6 · Cited by 282
Barber, G. N. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.12.015 · Cited by 287
Sensing damage by the NLRP3 inflammasome
Leemans, J. C., Cassel, S. L., & Sutterwala, F. S. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01043.x · Cited by 281
The Control of Adaptive Immune Responses by the Innate Immune System
Schenten, D., & Medzhitov, R. M. (2011) · Advances in immunology · doi:10.1016/b978-0-12-387664-5.00003-0 · Cited by 290
Cyclic di-GMP Sensing via the Innate Immune Signaling Protein STING
Yin, Q., Tian, Y., Kabaleeswaran, V., Jiang, X., Tu, D., Eck, M. J., Chen, Z. J., & Wu, H. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.05.029 · Cited by 293
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
Pyroptotic Neuronal Cell Death Mediated by the AIM2 Inflammasome
Adamczak, S. E., Vaccari, J. P. D. R., Dale, G. A., Brand, F. J., Nonner, D., Bullock, M. R. R., Dahl, G., Dietrich, W. D., & Keane, R. W. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.236 · Cited by 289
TLR8: the forgotten relative revindicated
Cervantes, J., Weinerman, B., Basole, C. P., & Salazar, J. C. (2012) · Cellular and Molecular Immunology · doi:10.1038/cmi.2012.38 · Cited by 283
Inhibition of cGAS DNA Sensing by a Herpesvirus Virion Protein
Wu, J., Li, W., Shao, Y., Avey, D. R., Fu, B., Gillen, J., Hand, T. H., Ma, S., Liu, X., Miley, W., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.07.015 · Cited by 278
Jia, C., Zhang, J., Chen, H. A., Zhuge, Y., Chen, H., Qian, F., Zhou, K., Niu, C., Wang, F., Qiu, H., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-2021-3 · Cited by 278
Inhibition of double‐strand DNA‐sensing cGAS ameliorates brain injury after ischemic stroke
Li, Q., Cao, Y., Dang, C., Han, B., Han, R., Ma, H., Hao, J., & Wang, L. (2020) · EMBO Molecular Medicine · doi:10.15252/emmm.201911002 · Cited by 284
Cytosolic DNA sensing by cGAS: regulation, function, and human diseases
Yu, L., & Liu, P. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00554-y · Cited by 295
Dissecting How CD4 T Cells Are Lost During HIV Infection
Doitsh, G., & Greene, W. C. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.02.012 · Cited by 291
Wang, Y., Ning, X., Gao, P., Wu, S., Sha, M., Lv, M., Zhou, X., Gao, J., Fang, R., Meng, G., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.011 · 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
(1,3)-β-Glucans Activate Both Dectin-1 and NLRP3 Inflammasome in Human Macrophages
Kankkunen, P., Teirilä, L., Rintahaka, J., Alenius, H. T., Wolff, H. J., & Matikainen, S. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903019 · Cited by 282
Innate Immune Recognition in Infectious and Noninfectious Diseases of the Lung
Opitz, B., van Laak, V., Eitel, J., & Suttorp, N. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200909-1427so · Cited by 287
Mechanism and regulation of pyroptosis-mediated in cancer cell death
Ruan, J., Wang, S., & Wang, J. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109052 · Cited by 276
Karki, R., Man, S. M., Malireddi, R. K. S., Gurung, P., Vogel, P., Lamkanfi, M., & Kanneganti, T.-D. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.01.006 · Cited by 272
He, Y., Varadarajan, S., Muñoz-Planillo, R., Burberry, A., Nakamura, Y., & Núñez, G. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.515080 · Cited by 275
The Inflammasome Puts Obesity in the Danger Zone
Stienstra, R., Tack, C. J., Kanneganti, T., Joosten, L. A. B., & Netea, M. G. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2011.10.011 · Cited by 275
Johnson, K. E., Chikoti, L., & Chandran, B. (2013) · Journal of Virology · doi:10.1128/jvi.00082-13 · Cited by 271
Research Advances in How the cGAS-STING Pathway Controls the Cellular Inflammatory Response
Wan, D., Jiang, W., & Hao, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00615 · Cited by 270
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
Pierini, R., Juruj, C., Perret, M., Jones, C., Mangeot, P.-E., Weiss, D. S., & Henry, T. (2012) · Cell Death and Differentiation · doi:10.1038/cdd.2012.51 · Cited by 278
NLRP1-Dependent Pyroptosis Leads to Acute Lung Injury and Morbidity in Mice
Kovářová, M., Hesker, P. R., Jania, L. A., Nguyen, M., Snouwaert, J. N., Xiang, Z., Lommatzsch, S. E., Huang, M. T.-H., Ting, J. P. ‐., & Koller, B. H. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201065 · Cited by 271
Role of pyroptosis in cardiovascular diseases
Jia, C., Chen, H. A., Zhang, J., Zhou, K., Zhuge, Y., Niu, C., Qiu, J., Rong, X., Shi, Z., Xiao, J., et al. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.12.028 · Cited by 268
Dampened STING-Dependent Interferon Activation in Bats
Xie, J., Li, Y., Shen, X.-R., Goh, G., Zhu, Y., Cui, J., Wang, L., Shi, Z., & Zhou, P. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.01.006 · Cited by 277
Gasdermin D Restrains Type I Interferon Response to Cytosolic DNA by Disrupting Ionic Homeostasis
Banerjee, I., Behl, B., Mendonça, M. S. A., Shrivastava, G., Russo, A. J., Ménoret, A., Ghosh, A., Vella, A. T., Vanaja, S. K., Sarkar, S. N., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.07.006 · Cited by 266
Self-citationInnate Immune Cell Death in Neuroinflammation and Alzheimer’s Disease
Rajesh, Y., & Kanneganti, T. (2022) · Cells · doi:10.3390/cells11121885 · Cited by 269
NLRP3 inflammasome inhibition is disrupted in a group of auto-inflammatory disease CAPS mutations
Mortimer, L. M., Moreau, F., MacDonald, J. A., & Chadee, K. (2016) · Nature Immunology · doi:10.1038/ni.3538 · Cited by 272
Inflammasomes in Tissue Damages and Immune Disorders After Trauma
Bortolotti, P., Faure, E., & Kipnis, É. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01900 · Cited by 268
Role of the Inflammasome, IL-1 β , and IL-18 in Bacterial Infections
Sahoo, M., Ceballos‐Olvera, I., del Barrio, L., & Re, F. (2011) · The Scientific World JOURNAL · doi:10.1100/2011/212680 · Cited by 269
Innate Immune Recognition of an AT-Rich Stem-Loop DNA Motif in the Plasmodium falciparum Genome
Sharma, S., DeOliveira, R. B., Kalantari, P., Parroche, P., Goutagny, N., Jiang, Z., Chan, J., Bartholomeu, D. C., Lauw, F. N., Hall, J. P., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.05.016 · Cited by 258
Self-citationMolecular mechanisms of inflammasome activation during microbial infections
Brož, P., & Monack, D. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01041.x · Cited by 266
The role of inflammasomes in human diseases and their potential as therapeutic targets
Yao, J., Sterling, K., Wang, Z., Zhang, Y., & Song, W. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01687-y · Cited by 260
Listeria monocytogenes is sensed by the NLRP3 and AIM2 inflammasome
Kim-Hellmuth, S., Bauernfeind, F. G., Ablasser, A., Hartmann, G., Fitzgerald, K. A., Latz, E., & Hornung, V. (2010) · European Journal of Immunology · doi:10.1002/eji.201040425 · Cited by 262
Self-citationHerzner, A., Hagmann, C. A., Goldeck, M., Wolter, S., Kübler, K., Wittmann, S., Gramberg, T., Andreeva, L., Hopfner, K., Mertens, C., et al. (2015) · Nature Immunology · doi:10.1038/ni.3267 · Cited by 255
Self-citationMechanisms governing inflammasome activation, assembly and pyroptosis induction
Kesavardhana, S., & Kanneganti, T. (2017) · International Immunology · doi:10.1093/intimm/dxx018 · Cited by 259
Ohkuri, T., Ghosh, A., Kosaka, A., Zhu, J., Ikeura, M., David, M., Watkins, S. C., Sarkar, S. N., & Okada, H. (2014) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-14-0099 · Cited by 255
Current Approaches Targeting the Wound Healing Phases to Attenuate Fibrosis and Scarring
Ayadi, A. E., Jay, J. W., & Prasai, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031105 · Cited by 262
Cytosolic DNA Sensing in Organismal Tumor Control
Vanpouille-Box, C., Demaria, S., Formenti, S. C., & Galluzzi, L. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.05.013 · Cited by 250
Yi, Y. (2017) · Immunology · doi:10.1111/imm.12787 · Cited by 256
Particulate formulations for the delivery of poly(I:C) as vaccine adjuvant
Hafner, A. M., Corthésy, B., & Merkle, H. P. (2013) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2013.05.013 · Cited by 254
Cytoplasmic DNA innate immune pathways
Barber, G. N. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01051.x · Cited by 254
McAuley, J., Tate, M. D., Mackenzie-Kludas, C., Pinar, A. A., Zeng, W., Stutz, A., Latz, E., Brown, L. E., & Mansell, A. S. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003392 · Cited by 258
Self-citationChavarría‐Smith, J., & Vance, R. E. (2015) · Immunological Reviews · doi:10.1111/imr.12283 · Cited by 247
Segovia, J. A., Sabbah, A., Mgbemena, V. E., Tsai, S.-Y., Chang, T.-H., Berton, M. T., Morris, I. R., Allen, I. C., Ting, J. P. ‐., & Bose, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029695 · Cited by 247
Innate immune detection of microbial nucleic acids
Gürtler, C., & Bowie, A. G. (2013) · Trends in Microbiology · doi:10.1016/j.tim.2013.04.004 · Cited by 251
Virus-cell fusion as a trigger of innate immunity dependent on the adaptor STING
Holm, C. K., Jensen, S. B., Jakobsen, M. R., Cheshenko, N., Horan, K., Moeller, H. B., Gonzalez‐Dosal, R., Rasmussen, S. B., Christensen, M. H., Yarovinsky, T. O., et al. (2012) · Nature Immunology · doi:10.1038/ni.2350 · Cited by 253
Self-citationMitochondrial DNA-triggered innate immune response: mechanisms and diseases
Hu, M.-M., & Shu, H. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01086-x · Cited by 263
Zhang, Z., Bao, M., Lu, N., Weng, L., Yuan, B., & Liu, Y. (2012) · Nature Immunology · doi:10.1038/ni.2492 · Cited by 249
Inflammasome-Mediated Inflammation in Liver Ischemia-Reperfusion Injury
Jiménez‐Castro, M. B., Cornide‐Petronio, M. E., Gracia‐Sancho, J., & Peralta, C. (2019) · Cells · doi:10.3390/cells8101131 · Cited by 244
IL-1β Signaling Promotes CNS-Intrinsic Immune Control of West Nile Virus Infection
Ramos, H. J., Lanteri, M. C., Blahnik, G., Negash, A. A., Suthar, M. S., Brassil, M. M., Sodhi, K., Treuting, P. M., Busch, M. P., Norris, P. J., et al. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1003039 · Cited by 240
Sweeten PAMPs: Role of sugar complexed PAMPs in innate immunity and vaccine biology
Mahla, R. S. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00248 · Cited by 239
The interferon response to intracellular DNA: Why so many receptors?
Unterholzner, L. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.07.007 · Cited by 248
The NLRP3 and Pyrin Inflammasomes: Implications in the Pathophysiology of Autoinflammatory Diseases
de Torre‐Minguela, C., Mesa-del-Castillo, P., & Pelegrín, P. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00043 · Cited by 251
Regulation of NLRP3 Inflammasome by Phosphorylation
Song, N., & Li, T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02305 · Cited by 239
AIM2 in health and disease: Inflammasome and beyond
Kumari, P. H., Russo, A. J., Shivcharan, S., & Rathinam, V. A. K. (2020) · Immunological Reviews · doi:10.1111/imr.12903 · Cited by 250
Danger-associated molecular patterns in Alzheimer’s disease
Venegas, C., & Heneka, M. T. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3mr0416-204r · Cited by 236
Chavarría‐Smith, J., & Vance, R. E. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003452 · Cited by 248
Opdenbosch, N. V., Gurung, P., Walle, L. V., Fossoul, A., Kanneganti, T., & Lamkanfi, M. (2014) · Nature Communications · doi:10.1038/ncomms4209 · Cited by 235
Inflammasomes as therapeutic targets in human diseases
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
Wu, D. Q., Wang, S., Yu, G., & Chen, X. S. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202010281 · Cited by 234
Exosome-inflammasome crosstalk and their roles in inflammatory responses
Noonin, C., & Thongboonkerd, V. (2021) · Theranostics · doi:10.7150/thno.54004 · Cited by 234
Necroinflammation in Kidney Disease
Mulay, S. R., Linkermann, A., & Anders, H. (2015) · Journal of the American Society of Nephrology · doi:10.1681/asn.2015040405 · Cited by 233
Role of pyroptosis in spinal cord injury and its therapeutic implications
Mamun, A. A., Wu, Y., Monalisa, I., Jia, C., Zhou, K., Munir, F., & Xiao, J. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.08.004 · Cited by 232
Metabolic crosstalk between host and pathogen: sensing, adapting and competing
Olive, A. J., & Sassetti, C. M. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.12 · Cited by 231
The Regulation of Inflammation by Innate and Adaptive Lymphocytes
Cronkite, D. A., & Strutt, T. M. (2018) · Journal of Immunology Research · doi:10.1155/2018/1467538 · Cited by 239
Tsourouktsoglou, T.-D., Warnatsch, A., Ιωάννου, Μ., Hoving, D., Wang, Q., & Papayannopoulos, V. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107602 · Cited by 227
Human Cytomegalovirus Tegument Protein pUL83 Inhibits IFI16-Mediated DNA Sensing for Immune Evasion
Li, T., Chen, J., & Cristea, I. M. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.10.007 · Cited by 226
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
Evasion of host immune defenses by human papillomavirus
Westrich, J. A., Warren, C. J., & Pyeon, D. (2016) · Virus Research · doi:10.1016/j.virusres.2016.11.023 · Cited by 225
AIM2 inflammasome activation and regulation: A structural perspective
Wang, B., & Yin, Q. (2017) · Journal of Structural Biology · doi:10.1016/j.jsb.2017.08.001 · Cited by 225
Recognition of bacterial infection by innate immune sensors
Kumar, S., Ingle, H., Prasad, D. V. R., & Kumar, H. (2012) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2012.706249 · Cited by 232
The PYHIN protein family as mediators of host defenses
Schattgen, S., & Fitzgerald, K. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01053.x · Cited by 224
Self-citationAIM2 inflammasome surveillance of DNA damage shapes neurodevelopment
Lammert, C. R., Frost, E. L., Bellinger, C. E., Bolte, A. C., McKee, C. A., Hurt, M. E., Paysour, M. J., Ennerfelt, H. E., & Lukens, J. R. (2020) · Nature · doi:10.1038/s41586-020-2174-3 · Cited by 223
Extensive evolutionary and functional diversity among mammalian AIM2-like receptors
Brunette, R. L., Young, J. M., Whitley, D. G., Brodsky, I. E., Malik, H. S., & Stetson, D. B. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20121960 · Cited by 230
Mechanisms of uric acid crystal‐mediated autoinflammation
Martinon, F. (2009) · Immunological Reviews · doi:10.1111/j.0105-2896.2009.00860.x · Cited by 226
RIG-I-like receptors: Sensing and responding to RNA virus infection
Nakhaei, P., Génin, P., Civas, A., & Hiscott, J. B. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.05.001 · Cited by 229
The role of the NLRP3 inflammasome in gout
McDermott, M., Kingsbury, S. R., & Conaghan, P. G. (2011) · Journal of Inflammation Research · doi:10.2147/jir.s11330 · Cited by 225
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
Verway, M. J., Bouttier, M., Wang, T. T., Carrier, M., Calderon, M. R., An, B., Devemy, E., McIntosh, F. A., Divangahi, M., Behr, M. A., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003407 · Cited by 222
Xia, P., Ye, B., Wang, S., Zhu, X., Du, Y., Xiong, Z., Tian, Y., & Fan, Z. (2016) · Nature Immunology · doi:10.1038/ni.3356 · Cited by 220
Inflammatory Stimuli Regulate Caspase Substrate Profiles
Agard, N. J., Maltby, D. A., & Wells, J. A. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m900528-mcp200 · Cited by 226
Activation of NLRP3 and AIM2 Inflammasomes by Porphyromonas gingivalis Infection
Park, E.-J., Na, H. S., Song, Y., Shin, S. Y., Kim, Y., & Chung, J. (2013) · Infection and Immunity · doi:10.1128/iai.00862-13 · Cited by 224
Metadata
- Authors
- Hornung, V., Ablasser, A., Charrel-Dennis, M., Bauernfeind, F., Horvath, G., Caffrey, D. R., Latz, E., & Fitzgerald, K. A.
- Affiliations
- University of Massachusetts Chan Medical School (US)
- Pfizer (United States) (US)
- Corresponding author
- Hornung, Veit
- Fitzgerald, Katherine A.
- Venue
- Nature
- Published
- 2009-01-21
- Volume
- 458
- Issue
- 7237
- Pages
- 514-518
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2726264
- OpenAlex
- W2042816890
- Cited by
- 2,627
- References
- 30
- Citations by year
- 2026: 108 · 2025: 164 · 2024: 187 · 2023: 152 · 2022: 168 · 2021: 162 · 2020: 158 · 2019: 146 · 2018: 142 · 2017: 137 · 2016: 142 · 2015: 144 · 2014: 147 · 2013: 168 · 2012: 140
- FWCI
- 66.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (AI065483, R01AI067497, R37AI067497, AI-067497, R01AI065483, R56AI067497)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- AIM2, cytosolic DNA sensing, inflammasome, caspase-1 activation, ASC, pyrin domain, double-stranded DNA, vaccinia virus, NF-κB activation, innate immunity, autoinflammation, autoimmunity, IL-1β, IL-18
- MeSH terms
- Animals, Cell Line, Cytoskeletal Proteins, Cytosol, DNA, DNA-Binding Proteins, Enzyme Activation, Humans, Inflammation, Nuclear Proteins, Poly dA-dT, Protein Binding, Vaccinia virus, Cell Death, Caspase 1, Apoptosis Regulatory Proteins, Mice, CARD Signaling Adaptor Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review