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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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An, R., Ni, Z., Xie, E., Rey, F. E., Kendziorski, C. M., & Thibeault, S. L. (2024) · iScience · doi:10.1016/j.isci.2024.110156 · Cited by 14
Gillette, D. D., Tridandapani, S., & Butchar, J. P. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00018 · Cited by 14
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
Generalized semi-refolding methods for purification of the functional death domain superfamily
Jang, T.-H., & Park, H. H. (2011) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2011.01.003 · Cited by 14
Induction of interferon and cell death in response to cytosolic DNA in chicken macrophages
Vitak, N., Hume, D. A., Chappell, K. J., Sester, D. P., & Stacey, K. J. (2016) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2016.01.023 · Cited by 14
The Role of CARD9 in Metabolic Diseases
Tian, C., Tuo, Y., Lu, Y. H., Xu, C., & Xiang, M. (2020) · Current Medical Science · doi:10.1007/s11596-020-2166-4 · Cited by 14
Bacterial DNA Promotes Proliferation of Rat Pancreatic Stellate Cells Thorough Toll-Like Receptor 9
Nakamura, T., Ito, T., Oono, T., Igarashi, H., Fujimori, N., Uchida, M., Niina, Y., Yasuda, M., Suzuki, K., & Takayanagi, R. (2011) · Pancreas · doi:10.1097/mpa.0b013e318224a501 · Cited by 14
Gratz, M. S., Suezer, Y., Kremer, M., Volz, A., Majzoub, M., Hanschmann, K.-M. O., Kalinke, U., Schwantes, A., & Sutter, G. (2011) · Journal of Virology · doi:10.1128/jvi.01191-10 · Cited by 14
AIM2 promotes TH17 cells differentiation by regulating RORγt transcription activity
Leite, J. A., Menezes-Silva, L., Martins, E., Rodrigues, T. S., Tavares, L., Ebering, A., Schelmbauer, C., Cebinelli, G. C. M., Zinina, V. V., Golden, A., et al. (2023) · iScience · doi:10.1016/j.isci.2023.108134 · Cited by 13
Advances in the mechanism of inflammasomes activation in herpes virus infection
Chen, H., Jian, Z., Xu, T. W., Xu, L., Deng, L., Shao, L., Zhang, L., He, L. Q., Li, Y., & Zhu, L. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1346878 · Cited by 13
The roles of AIM2 in neurodegenerative diseases: insights and therapeutic implications
Yang, K., Wang, X. L., Pan, H., Wang, X., Hu, Y., Yao, Y.-H., Zhao, X., & Sun, T. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1441385 · Cited by 15
Qi, Y., Li, M., Liu, Q., Li, F., Zhu, B., Wang, J., Lu, Y., Liu, J., Wu, J., Zheng, X., et al. (2016) · Scientific Reports · doi:10.1038/srep28776 · Cited by 13
Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19
Brain, D. E., Plant-Hately, A. J., Heaton, B. J., Arshad, U., David, C. A. W., Hedrich, C. M., Owen, A., & Liptrott, N. J. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.113848 · Cited by 13
Wallace, H. L., & Russell, R. S. (2022) · Viruses · doi:10.3390/v14102113 · Cited by 15
Buso, G., Faggin, E., Rosenblatt‐Velin, N., Pellegrin, M., Galliazzo, S., Calanca, L., Rattazzi, M., & Mazzolai, L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021169 · Cited by 13
Luo, F., Liu, H., Yang, S., Fang, Y., Zhao, Z., Hu, Y., Jin, Y., Li, P., Gao, T., Cao, C., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1800461 · Cited by 13
Hou, X., & Niu, X. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.04.046 · Cited by 13
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Yang, F., Dai, Z., Xue, M.-Y., Chen, X.-Y., Liu, J., Li, W., Xu, L., & Di, B. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c00343 · Cited by 12
AIM2 enhances Candida albicans infection through promoting macrophage apoptosis via AKT signaling
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Senapati, S., Bertolini, T. B., Minnier, M. A., Yazicioglu, M. N., Markusic, D. M., Zhang, R., Wicks, J. R., Nahvi, A., Herzog, R. W., Walsh, M. C., et al. (2025) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2025.102502 · Cited by 12
The type I interferon response during viral infections: a “SWOT” analysis
Gaajetaan, G. R., Bruggeman, C. A., & Stassen, F. R. M. (2011) · Reviews in Medical Virology · doi:10.1002/rmv.713 · Cited by 12
Sung, M. W., Watts, T., & Li, P. (2012) · Acta Crystallographica Section F Structural Biology and Crystallization Communications · doi:10.1107/s174430911203103x · Cited by 12
AIM2 Inflammasome Is Critical for dsDNA-Induced IL-1β Secretion in Human Dental Pulp Cells
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Marín‐Aguilar, F., Ruı́z-Cabello, J., & Cordero, M. D. (2018) · Experientia supplementum · doi:10.1007/978-3-319-89390-7_13 · Cited by 12
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Inflammation initiated by stressed organelles
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Guzova, J. A., Primiano, M. J., Jiao, A., Stock, J. L., Lee, C., Winkler, A. R., & Hall, J. P. (2019) · Journal of Immunological Methods · doi:10.1016/j.jim.2019.02.002 · Cited by 12
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Cao, A., Devant, P., Wang, C., Sun, M., Kennedy, S. N., Ma, W., Ruan, J., & Kagan, J. C. (2025) · Science Advances · doi:10.1126/sciadv.adt9027 · Cited by 12
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Richard, K., Mann, B. J., Qin, A., Barry, E. M., Ernst, R. K., & Vogel, S. N. (2017) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00574-16 · Cited by 11
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Wu, S., Ye, X., Wang, J., Li, M., Fu, Y., & Wang, S. (2026) · Neoplasia · doi:10.1016/j.neo.2026.101290 · Cited by 11
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Biron, C. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800964-2.00004-5 · Cited by 12
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Pietrobon, A. J., Yoshikawa, F. S. Y., de Oliveira, L. M., Pereira, N. Z., Matozo, T., de Alencar, B. C., Duarte, A. J. S., & Sato, M. N. (2021) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiab389 · Cited by 10
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Bao, Z., Deng, Y., Qian, Z., & Zhuang, Y. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2907254 · Cited by 9
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Song, W., Le, S., Chen, F., Tian, Y., Li, L., Wang, G., Li, H., & Cai, Y. (2020) · Cell Stress and Chaperones · doi:10.1007/s12192-019-01065-0 · Cited by 9
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Pyroptosis in Skeleton Diseases: A Potential Therapeutic Target Based on Inflammatory Cell Death
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Kumari, M. S. K. M., Liu, P., Nitchman, M. S., Chaudhary, S., Jump, K., Morales, Y., Miller, E., Shecter, I., Stadecker, M. J., & Kalantari, P. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1012108 · Cited by 8
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Marion, M. C., Ramos, P. S., Bachali, P., Labonte, A. C., Zimmerman, K. D., Ainsworth, H. C., Heuer, S. E., Robl, R. D., Catalina, M. D., Kelly, J. A., et al. (2021) · Genes · doi:10.3390/genes12121898 · Cited by 8
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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