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The AIM2 inflammasome is essential for host defense against cytosolic bacteria and DNA viruses
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Inflammasomes regulate the activity of caspase-1 and the maturation of interleukin 1beta (IL-1beta) and IL-18. AIM2 has been shown to bind DNA and engage the caspase-1-activating adaptor protein ASC to form a caspase-1-activating inflammasome. Using Aim2-deficient mice, we identify a central role for AIM2 in regulating caspase-1-dependent maturation of IL-1beta and IL-18, as well as pyroptosis, in response to synthetic double-stranded DNA. AIM2 was essential for inflammasome activation in response to Francisella tularensis, vaccinia virus and mouse cytomegalovirus and had a partial role in the sensing of Listeria monocytogenes. Moreover, production of IL-18 and natural killer cell-dependent production of interferon-gamma, events critical in the early control of virus replication, were dependent on AIM2 during mouse cytomegalovirus infection in vivo. Collectively, our observations demonstrate the importance of AIM2 in the sensing of both bacterial and viral pathogens and in triggering innate immunity.
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“Finally, the authors found no secretion of the proinflammatory cytokine interleukin-1β, a process known to depend on the inflammasome—a caspase-1-containing complex (122).”
From The Impact of Mass Spectrometry–Based Proteomics on Fundamental Discoveries in Virology (2014) · cites this paper as [122]
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“AIM2 has a demonstrated role in immune responses directed against both bacteria51 and DNA viruses52, but it will be important to determine whether there is a physiological role for AIM2 in sterile inflammation, especially in autoimmune diseases such as systemic lupus erythematosus, which is associated with elevated circulating levels of dsDNA.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [52]
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Cites
Biologic basis for interleukin-1 in disease.
Dinarello, C. (1996) · Blood · doi:10.1182/blood.v87.6.2095.bloodjournal8762095 · Cited by 4,344
Immunological and inflammatory functions of the interleukin-1 family
Dinarello, C. A. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132612 · Cited by 3,466
Toll-like receptors in innate immunity
Takeda, K. (2004) · International Immunology · doi:10.1093/intimm/dxh186 · Cited by 3,328
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
STING regulates intracellular DNA-mediated, type I interferon-dependent innate immunity
Ishikawa, H., Ma, Z., & Barber, G. N. (2009) · Nature · doi:10.1038/nature08476 · Cited by 2,759 · cited 1×
“The IFN inducing pathway is complex and involves RNA polymerase III, and one or more redundant sensors, which collectively converge on a signaling axis involving STING 38 , TANK Binding Kinase-1 39 and the Interferon Regulatory Factors (IRF3 and IRF7) (reviewed in 37 ).”
IKKε and TBK1 are essential components of the IRF3 signaling pathway
Fitzgerald, K. A., McWhirter, S. M., Faia, K. L., Rowe, D. C., Latz, E., Golenbock, D. T., Coyle, A. J., Liao, S.-M., & Maniatis, T. (2003) · Nature Immunology · doi:10.1038/ni921 · Cited by 2,680
Self-citationAIM2 recognizes cytosolic dsDNA and forms a caspase-1-activating inflammasome with ASC
Hornung, V., Ablasser, A., Charrel-Dennis, M., Bauernfeind, F., Horvath, G., Caffrey, D. R., Latz, E., & Fitzgerald, K. A. (2009) · Nature · doi:10.1038/nature07725 · Cited by 2,627
Self-citationThe Inflammasomes: Guardians of the Body
Martinon, F., Mayor, A., & Tschopp, J. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132715 · Cited by 2,436
AIM2 activates the inflammasome and cell death in response to cytoplasmic DNA
Fernandes-Alnemri, T., Yu, J.-W., Datta, P., Wu, J., & Alnemri, E. S. (2009) · Nature · doi:10.1038/nature07710 · Cited by 1,831
DAI (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
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Olsen, I., & Yilmaz, Ö. (2016) · Journal of Oral Microbiology · doi:10.3402/jom.v8.30385 · Cited by 112
Segovia, J. A., Chang, T.-H., Winter, V. T., Coalson, J. J., Cagle, M. P., Pandranki, L., Bose, S., Baseman, J. B., & Kannan, T. R. (2017) · Infection and Immunity · doi:10.1128/iai.00548-17 · Cited by 112
Peng, K., Brož, P., Jones, J. W. M., Joubert, L., & Monack, D. M. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01643.x · Cited by 110
Recognition of Herpes Simplex Viruses: Toll-Like Receptors and Beyond
Ma, Y., & He, B. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.11.012 · Cited by 110
A Mechanism for the Inhibition of DNA-PK-Mediated DNA Sensing by a Virus
Peters, N., Ferguson, B. J., Mazzon, M., Fahy, A. S., Krysztofinska, E., Arribas-Bosacoma, R., Pearl, L. H., Ren, H., & Smith, G. L. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003649 · Cited by 113
Inflammasomes and Atherosclerosis: a Mixed Picture
Tall, A. R., & Bornfeldt, K. (2023) · Circulation Research · doi:10.1161/circresaha.123.321637 · Cited by 112
IKKα negatively regulates ASC-dependent inflammasome activation
Martin, B. N., Wang, C., Willette‐Brown, J., Herjan, T., Gulen, M. F., Zhou, H., Bulek, K., Franchi, L., Sato, T., Alnemri, E. S., et al. (2014) · Nature Communications · doi:10.1038/ncomms5977 · Cited by 116
Self-citationTargeting pattern recognition receptors in cancer immunotherapy
Goutagny, N., Estornes, Y., Hasan, U. A., Lebecque, S., & Caux, C. (2012) · Targeted Oncology · doi:10.1007/s11523-012-0213-1 · Cited by 113
An Update on PYRIN Domain-Containing Pattern Recognition Receptors: From Immunity to Pathology
Ratsimandresy, R. A., Dorfleutner, A., & Stehlik, C. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00440 · Cited by 114
Stressing out the mitochondria: Mechanistic insights into NLRP3 inflammasome activation
Yabal, M., Calleja, D. J., Simpson, D. S., & Lawlor, K. E. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.mr0318-124r · Cited by 110
Involvement of NLRP3 inflammasome in CVB3-induced viral myocarditis
Wang, Y., Gao, B., & Xiong, S. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00441.2014 · Cited by 109
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Kumar, H., Pandey, S., Zou, J., Kumagai, Y., Takahashi, K., Akira, S., & Kawai, T. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1002094 · Cited by 108
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McVey, M. J., Steinberg, B. E., & Goldenberg, N. M. (2020) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00303.2020 · Cited by 108
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Khairallah, C. F., Déchanet‐Merville, J., & Capone, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00105 · Cited by 114
Ekchariyawat, P., Hamel, R., Bernard, É., Wichit, S., Surasombatpattana, P., Talignani, L., Frédéric Thomas, A., Choumet, V., Yssel, H., Desprès, P., et al. (2015) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2015.03.025 · Cited by 106
Sampson, T. R., Napier, B. A., Schroeder, M. R., Louwen, R., Zhao, J., Chin, C., Ratner, H. K., Llewellyn, A. C., Jones, C. L., Laroui, H., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323025111 · Cited by 105
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Sparrer, K. M. J., & Gack, M. U. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.03.001 · Cited by 105
Hamon, M. A., & Cossart, P. (2011) · Infection and Immunity · doi:10.1128/iai.01243-10 · Cited by 105
CLEC5A is a critical receptor in innate immunity against Listeria infection
Chen, S.-T., Li, F.-J., Hsu, T.-Y., Liang, S., Yeh, Y., Liao, W.-Y., Chou, T., Chen, N.-J., Hsiao, M., Yang, W., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00356-3 · Cited by 104
Lipids, inflammasomes, metabolism, and disease
Anand, P. (2020) · Immunological Reviews · doi:10.1111/imr.12891 · Cited by 108
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Alu, A., Han, X., Ma, X., Wu, M., Wei, Y., & Wei, X. (2020) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2020.07.003 · Cited by 109
Baum, R., Sharma, S., Carpenter, S. B., Li, Q., Busto, P., Fitzgerald, K. A., Marshak‐Rothstein, A., & Gravallese, E. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1402573 · Cited by 104
Self-citationSorrentino, R., Terlizzi, M., Crescenzo, V. G. D., Popolo, A., Pecoraro, M., Perillo, G., Galderisi, A., & Pinto, A. (2015) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.07.009 · Cited by 103
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Signaling Through Nucleic Acid Sensors and Their Roles in Inflammatory Diseases
Okude, H., Ori, D., & Kawai, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.625833 · Cited by 104
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Control of antiviral immunity by pattern recognition and the microbiome
Pang, I. K., & Iwasaki, A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01073.x · Cited by 106
Lee, B. H., Hwang, D. M., Palaniyar, N., Grinstein, S., Philpott, D. J., & Hu, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035812 · Cited by 102
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NLRs, inflammasomes, and viral infection
Jacobs, S. R., & Damania, B. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0312132 · Cited by 104
Lam, E. P. S., Kariyawasam, H. H., Rana, B. M. J., Durham, S. R., McKenzie, A. N. J., Powell, N., Orban, N. T., Lennartz-Walker, M., Hopkins, C. L., Ying, S., et al. (2015) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.10.019 · Cited by 101
Baatarjav, C., Komada, T., Karasawa, T., Yamada, N., Sampilvanjil, A., Matsumura, T., & Takahashi, M. (2022) · Cell Death and Differentiation · doi:10.1038/s41418-022-01033-9 · Cited by 102
Inflammatory caspases: key regulators of inflammation and cell death
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Hofbauer, D., Mougiakakos, D., Broggini, L., Zaiss, M., Büttner-Herold, M., Bach, C., Spriewald, B., Neumann, F., Bisht, S., Nolting, J., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.07.002 · Cited by 100
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The emerging roles of inflammasome‐dependent cytokines in cancer development
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AIM2 controls microglial inflammation to prevent experimental autoimmune encephalomyelitis
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Nour, A. M., Reichelt, M., Ku, C., Ho, M.-Y., Heineman, T. C., & Arvin, A. M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.210575 · Cited by 100
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Wang, J., Li, R., Peng, Z., Hu, B., Rao, X., & Li, J. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4530 · Cited by 98
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Oviedo-Boyso, J., Bravo-Patiño, A., & Baizabal-Aguirre, V. M. (2014) · Mediators of Inflammation · doi:10.1155/2014/432785 · Cited by 101
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Ran, Y., Shu, H., & Wang, Y. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.05.003 · Cited by 96
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Yuk, J., Silwal, P., & Jo, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134714 · Cited by 98
HUWE1 mediates inflammasome activation and promotes host defense against bacterial infection
Guo, Y., Li, L., Xu, T., Guo, X., Wang, C., Li, Y., Yang, Y., Yang, D., Sun, B., Zhao, X., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci138234 · Cited by 96
Duan, X., Ponomareva, L. V., Veeranki, S., Panchanathan, R., Dickerson, E., & Choubey, D. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-10-0565 · Cited by 95
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Inhibition of AIM2 inflammasome activation by a novel transcript isoform of IFI16
Wang, P., Ye, Z., Deng, J., Siu, K., Gao, W., Chaudhary, V., Cheng, Y., Fung, S., Yuen, K., Ho, T., et al. (2018) · EMBO Reports · doi:10.15252/embr.201845737 · Cited by 94
GLUT1-dependent glycolysis regulates exacerbation of fibrosis via AIM2 inflammasome activation
Cho, S. J., Moon, J., Nikahira, K., Yun, H. S., Harris, R. A., Hong, K. S., Huang, H., Choi, A. M. K., & Stout-Delgado, H. W. (2019) · Thorax · doi:10.1136/thoraxjnl-2019-213571 · Cited by 91
GSDMD drives canonical inflammasome‐induced neutrophil pyroptosis and is dispensable for NETosis
Chauhan, D., Demon, D., Walle, L. V., Paerewijck, O., Zecchin, A., Bosseler, L., Santoni, K., Planès, R., Ribó, S., Fossoul, A., et al. (2022) · EMBO Reports · doi:10.15252/embr.202154277 · Cited by 94
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Critical role for the AIM 2 inflammasome during acute CNS bacterial infection
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Subversion of inflammasome activation and pyroptosis by pathogenic bacteria
Cunha, L. D., & Zamboni, D. S. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00076 · Cited by 93
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Palmai‐Pallag, T., & Bachrati, C. Z. (2014) · Microbes and Infection · doi:10.1016/j.micinf.2014.10.001 · Cited by 88
DDX24 Negatively Regulates Cytosolic RNA-Mediated Innate Immune Signaling
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Inflammasomes in Respiratory Disease
Brusselle, G., Provoost, S., Bracke, K. R., Kuchmiy, A. A., & Lamkanfi, M. (2014) · CHEST Journal · doi:10.1378/chest.13-1885 · Cited by 87
Cannabinoids as Key Regulators of Inflammasome Signaling: A Current Perspective
Suryavanshi, S. V., Kovalchuk, I., & Kovalchuk, O. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.613613 · Cited by 87
Brodmann, M., Dreier, R. F., Brož, P., & Basler, M. (2017) · Nature Communications · doi:10.1038/ncomms15853 · Cited by 91
Viral-mediated activation and inhibition of programmed cell death
Verburg, S. G., Lelievre, R. M., Westerveld, M. J., Inkol, J. M., Sun, Y. L., & Workenhe, S. T. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010718 · Cited by 87
Sun, C., Schattgen, S., Pisitkun, P., Jørgensen, J., Hilterbrand, A. T., Wang, L. J., West, J. A., Hansen, K., Horan, K., Jakobsen, M. R., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402495 · Cited by 85
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Bi, J., Song, S., Fang, L., Wang, D., Jing, H., Gao, L., Cai, Y., Luo, R., Chen, H., & Xiao, S. (2014) · Mediators of Inflammation · doi:10.1155/2014/403515 · Cited by 84
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Cyclic‐di‐GMP and cyclic‐di‐AMP activate the NLRP3 inflammasome
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Sharma, S., & Fitzgerald, K. A. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1001310 · Cited by 79
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Zhang, Z., Li, X., Wang, Y., Wei, Y., & Wei, X. (2023) · Journal of Hematology & Oncology · doi:10.1186/s13045-023-01407-7 · Cited by 83
Metadata
- Authors
- Rathinam, V. A. K., Jiang, Z., Waggoner, S. N., Sharma, S., Cole, L. E., Waggoner, L., Vanaja, S. K., Monks, B. G., Ganesan, S., Latz, E., Hornung, V., Vogel, S. N., Szomolanyi-Tsuda, E., & Fitzgerald, K. A.
- Affiliations
- University of Massachusetts Chan Medical School (US)
- University of Maryland, Baltimore (US)
- University of Bonn (DE)
- Corresponding author
- Fitzgerald, Katherine A
- ORCID
- Venue
- Nature Immunology
- Published
- 2010-03-28
- Volume
- 11
- Issue
- 5
- Pages
- 395-402
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC2887480
- OpenAlex
- W2104195963
- Cited by
- 1,331
- References
- 53
- Citations by year
- 2026: 42 · 2025: 52 · 2024: 74 · 2023: 64 · 2022: 66 · 2021: 68 · 2020: 80 · 2019: 89 · 2018: 70 · 2017: 89 · 2016: 95 · 2015: 90 · 2014: 103 · 2013: 108 · 2012: 72
- FWCI
- 44.92
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship@UMassChan (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Cancer Institute (CA 66644, R01CA066644, CA034461, R01CA034461)
- National Institute of Allergy and Infectious Diseases (AI-07349, U54 AI157168, AI083713, R01AI083713, T32AI007349)
- 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
- AIM2 inflammasome, caspase-1, IL-1β maturation, pyroptosis, innate immunity, cytosolic bacteria, DNA viruses, Francisella tularensis, vaccinia virus, murine cytomegalovirus, Listeria monocytogenes, interferon-gamma, natural killer cells, double-stranded DNA sensing
- MeSH terms
- Animals, Cell Line, Cytoskeletal Proteins, DNA, DNA Virus Infections, DNA Viruses, DNA-Binding Proteins, Francisella tularensis, Humans, Immunity, Innate, Killer Cells, Natural, Listeriosis, Lymphocyte Activation, Macrophages, Mice, Inbred C57BL, Nuclear Proteins, Transcription Factors, Tularemia, Signal Transduction, Cytokines, Mice, Knockout, Viral Load, Caspase 1, Multiprotein Complexes, Apoptosis Regulatory Proteins, Mice, CARD Signaling Adaptor Proteins
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