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The AIM2 inflammasome is essential for host defense against cytosolic bacteria and DNA viruses
Open accessAbstract
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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Citations
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
RNA Polymerase III Detects Cytosolic DNA and Induces Type I Interferons through the RIG-I Pathway
Chiu, Y., MacMillan, J. B., & Chen, Z. J. (2009) · Cell · doi:10.1016/j.cell.2009.06.015 · Cited by 1,185
Bürckstümmer, T., Baumann, C., Blüml, S., Dixit, E., Dürnberger, G., Jahn, H., Planyavsky, M., Bilban, M., Colinge, J., Bennett, K. L., et al. (2009) · Nature Immunology · doi:10.1038/ni.1702 · Cited by 1,091
Fernandes-Alnemri, T., Wu, J., Yu, J.-W., Datta, P., Miller, B., Jankowski, W., Rosenberg, S., Zhang, J., & Alnemri, E. S. (2007) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4402194 · Cited by 1,026
Toll‐like Receptor and RIG‐1‐like Receptor Signaling
Kawai, T., & Akira, S. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1443.020 · Cited by 1,014
Ablasser, A., Bauernfeind, F. G., Hartmann, G., Latz, E., Fitzgerald, K. A., & Hornung, V. (2009) · Nature Immunology · doi:10.1038/ni.1779 · Cited by 892
Self-citationNalp1b controls mouse macrophage susceptibility to anthrax lethal toxin
Boyden, E. D., & Dietrich, W. F. (2006) · Nature Genetics · doi:10.1038/ng1724 · Cited by 860
Innate immune detection of the type III secretion apparatus through the NLRC4 inflammasome
Miao, E. A., Mao, D. P., Yudkovsky, N., Bonneau, R., Lorang, C. G., Warren, S. E., Leaf, I. A., & Aderem, A. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913087107 · Cited by 838
HIN-200 Proteins Regulate Caspase Activation in Response to Foreign Cytoplasmic DNA
Roberts, T. L., Idris, A., Dunn, J. A., Kelly, G., Burnton, C. M., Hodgson, S., Hardy, L., Garceau, V., Sweet, M. J., Ross, I. L., et al. (2009) · Science · doi:10.1126/science.1169841 · Cited by 830
Inflammasome recognition of influenza virus is essential for adaptive immune responses
Ichinohe, T., Lee, H. K., Ogura, Y., Flavell, R. A., & Iwasaki, A. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20081667 · Cited by 701
Vital Involvement of a Natural Killer Cell Activation Receptor in Resistance to Viral Infection
Brown, M. G., Dokun, A. O., Heusel, J. W., Smith, H. R. C., Beckman, D. L., Blattenberger, E. A., Dubbelde, C., Stone, L. R., Scalzo, A. A., & Yokoyama, W. M. (2001) · Science · doi:10.1126/science.1060042 · Cited by 626
Kanneganti, T., Lamkanfi, M., Kim, Y., Chen, G., Park, J., Franchi, L., Vandenabeele, P., & Núñez, G. (2007) · Immunity · doi:10.1016/j.immuni.2007.03.008 · Cited by 537
Poeck, H., Bscheider, M., Groß, O., Finger, K., Roth, S., Rebsamen, M., Hannesschläger, N., Schlee, M., Rothenfußer, S., Barchet, W., et al. (2009) · Nature Immunology · doi:10.1038/ni.1824 · Cited by 518
Self-citationAlcamı́, A., & Smith, G. L. (1992) · Cell · doi:10.1016/0092-8674(92)90274-g · Cited by 478
The inflammasomes: mechanisms of activation and function
Latz, E. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2009.12.004 · Cited by 467
Self-citationDaniels, K. A., Devora, G. A., Lai, W. C., O’Donnell, C. L., Bennett, M., & Welsh, R. M. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.1.29 · Cited by 435
Lee, S.-H., Girard, S., Macina, D., Busà, M., Zafer, A., Belouchi, A., Gros, P., & Vidal, S. M. (2001) · Nature Genetics · doi:10.1038/ng0501-42 · Cited by 403
Innate immunity against Francisella tularensis is dependent on the ASC/caspase-1 axis
Mariathasan, S., Weiss, D. S., Dixit, V. M., & Monack, D. M. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050977 · Cited by 402
Absence of IL-1 signaling and reduced inflammatory response in IL-1 type I receptor-deficient mice.
Labow, M., Shuster, D., Zetterström, M., Nunes, P., Terry, R., Cullinan, E., Bártfai, T., Solórzano, C., Moldawer, L., Chizzonite, R., et al. (1997) · Journal of Immunology · doi:10.4049/jimmunol.159.5.2452 · Cited by 376
Inflammasomes: guardians of cytosolic sanctity
Lamkanfi, M., & Dixit, V. M. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00730.x · Cited by 372
Hornung, V., & Latz, E. (2010) · Nature reviews. Immunology · doi:10.1038/nri2690 · Cited by 366
Self-citationFranchi, L., Kanneganti, T.-D., Dubyak, G. R., & Núñez, G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m610762200 · Cited by 356
Henry, T., Brotcke, A., Weiss, D. S., Thompson, L. J., & Monack, D. M. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062665 · Cited by 323
Pathogenesis of murine cytomegalovirus infection in natural killer cell-depleted mice
Bukowski, J. F., Woda, B. A., & Welsh, R. M. (1984) · Journal of Virology · doi:10.1128/jvi.52.1.119-128.1984 · Cited by 286
Johnston, J. B., Barrett, J. W., Nazarian, S. H., Goodwin, M., Ricuttio, D., Wang, G., & McFadden, G. (2005) · Immunity · doi:10.1016/j.immuni.2005.10.003 · Cited by 232
Meixenberger, K., Pache, F. C., Eitel, J., Schmeck, B., Hippenstiel, S., Slevogt, H., N’Guessan, P. D., Witzenrath, M., Netea, M. G., Chakraborty, T., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901346 · Cited by 186
Multiple Nod-Like Receptors Activate Caspase 1 during Listeria monocytogenes Infection
Warren, S. E., Mao, D. P., Rodriguez, A. E., Miao, E. A., & Aderem, A. A. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.11.7558 · Cited by 182
Innate and Adaptive Immunity to Francisella
Elkins, K., Cowley, S. C., & Bosio, C. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1409.014 · Cited by 174
The HIN-200 family: More than interferon-inducible genes?
Ludlow, L. E. A., Johnstone, R. W., & Clarke, C. J. P. (2005) · Experimental Cell Research · doi:10.1016/j.yexcr.2005.03.032 · Cited by 170
The chemotherapeutic agent DMXAA potently and specifically activates the TBK1–IRF-3 signaling axis
Roberts, Z. J., Goutagny, N., Perera, P., Kato, H., Kumar, H., Kawai, T., Akira, S., Savan, R., Echo, D. V., Fitzgerald, K. A., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061845 · Cited by 167
Self-citationHuysamen, C., & Brown, G. D. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01418.x · Cited by 155
RIG-I family RNA helicases: Cytoplasmic sensor for antiviral innate immunity
Yoneyama, M., & Fujita, T. (2007) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2007.06.023 · Cited by 144
Cole, L. E., Shirey, K., Barry, E. M., Santiago, A. E., Rallabhandi, P., Elkins, K., Puche, A., Michalek, S., & Vogel, S. (2007) · Infection and Immunity · doi:10.1128/iai.01868-06 · Cited by 128
Self-citationScalzo, A. A., Lyons, P., Fitzgerald, N. A., Forbes, C. A., Yokoyama, W. M., & SHELLAM, G. R. (1995) · Genomics · doi:10.1006/geno.1995.1074 · Cited by 127
Smith, G. L., & Chan, Y. S. (1991) · Journal of General Virology · doi:10.1099/0022-1317-72-3-511 · Cited by 112
The Ifi 200 genes: An emerging family of IFN-inducible genes
Landolfo, S., Gariglio, M., Gribaudo, G., & Lembo, D. (1998) · Biochimie · doi:10.1016/s0300-9084(99)80025-x · Cited by 100
Henry, T., & Monack, D. M. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.01022.x · Cited by 90
Innate immune response to Francisella tularensis is mediated by TLR2 and caspase-1 activation
Li, H., Nookala, S., Bina, X. R., Bina, J. E., & Re, F. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0406294 · Cited by 88
Cole, L. E., Santiago, A. E., Barry, E. M., Kang, T. J., Shirey, K. A., Roberts, Z. J., Elkins, K. L., Cross, A. S., & Vogel, S. N. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.10.6885 · Cited by 82
Self-citationMcVicar, D. W., Winkler-Pickett, R. T., Taylor, L. S., Makrigiannis, A. P., Bennett, M., Anderson, S. K., & Ortaldo, J. R. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.4.1721 · Cited by 51
Pien, G. C., & Biron, C. A. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.2.994 · Cited by 47
Elkins, K. L., Winegar, R. K., Nacy, C. A., & Fortier, A. H. (1992) · Microbial Pathogenesis · doi:10.1016/0882-4010(92)90085-3 · Cited by 44
Rathinam, V. A. K., Hoag, K. A., & Mansfield, L. S. (2008) · Microbes and Infection · doi:10.1016/j.micinf.2008.07.030 · Cited by 37
Self-citationDinarello, C. A., Novick, D., Rubinstein, M., & Lonnemann, G. (2003) · Blood Purification · doi:10.1159/000070699 · Cited by 32
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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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