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The AIM2 inflammasome is critical for innate immunity to Francisella tularensis
Open accessAbstract
Francisella tularensis, the causative agent of tularemia, infects host macrophages, which triggers production of the proinflammatory cytokines interleukin 1beta (IL-1beta) and IL-18. We elucidate here how host macrophages recognize F. tularensis and elicit this proinflammatory response. Using mice deficient in the DNA-sensing inflammasome component AIM2, we demonstrate here that AIM2 is required for sensing F. tularensis. AIM2-deficient mice were extremely susceptible to F. tularensis infection, with greater mortality and bacterial burden than that of wild-type mice. Caspase-1 activation, IL-1beta secretion and cell death were absent in Aim2(-/-) macrophages in response to F. tularensis infection or the presence of cytoplasmic DNA. Our study identifies AIM2 as a crucial sensor of F. tularensis infection and provides genetic proof of its critical role in host innate immunity to intracellular pathogens.
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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 [51]
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Pathogen Recognition and Innate Immunity
Akira, S., Uematsu, S., & Takeuchi, O. (2006) · Cell · doi:10.1016/j.cell.2006.02.015 · Cited by 11,976
Bauernfeind, F. G., Horvath, G. L., Stutz, A., Alnemri, E. S., MacDonald, K. L., Speert, D. P., Fernandes‐Alnemri, T., Wu, J., Monks, B. G., Fitzgerald, K. A., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901363 · Cited by 3,087
Self-citationCryopyrin 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
AIM2 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
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
The 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
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
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
Self-citationFranchi, L., Amer, A., Body-Malapel, M., Kanneganti, T.-D., Özören, N., Jagirdar, R., Inohara, N., Vandenabeele, P., Bertin, J., Coyle, A., et al. (2006) · Nature Immunology · doi:10.1038/ni1346 · Cited by 1,131
Cytoplasmic flagellin activates caspase-1 and secretion of interleukin 1β via Ipaf
Miao, E. A., Alpuche-Aranda, C. M., Dors, M., Clark, A. E., Bader, M. W., Miller, S. I., & Aderem, A. (2006) · Nature Immunology · doi:10.1038/ni1344 · Cited by 1,127
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
Self-citationThe NLR Gene Family: A Standard Nomenclature
Ting, J. P. ‐., Lovering, R. C., Alnemri, E. S., Bertin, J., Boss, J. M., Davis, B. K., Flavell, R. A., Girardin, S. E., Godzik, A., Harton, J. A., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.02.005 · Cited by 998
Self-citationThe 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
Nalp1b controls mouse macrophage susceptibility to anthrax lethal toxin
Boyden, E. D., & Dietrich, W. F. (2006) · Nature Genetics · doi:10.1038/ng1724 · Cited by 882
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
Anti-inflammatory Compounds Parthenolide and Bay 11-7082 Are Direct Inhibitors of the Inflammasome
Juliana, C. A., Fernandes‐Alnemri, T., Wu, J., Datta, P., Solórzano, L., Yu, J., Meng, R., Quong, A. A., Latz, E., Scott, C. P., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.082305 · Cited by 630
Self-citationPathogen recognition in the innate immune response
Kumar, H., Kawai, T., & Akira, S. (2009) · Biochemical Journal · doi:10.1042/bj20090272 · Cited by 609
The PYRIN-CARD Protein ASC Is an Activating Adaptor for Caspase-1
Srinivasula, S. M., Poyet, J.-L., Razmara, M., Datta, P., Zhang, Z., & Alnemri, E. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.c200179200 · Cited by 573
Self-citationChae, J. J., Wood, G., Masters, S. L., Richard, K., Park, G. S. H., Smith, B. J., & Kastner, D. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602081103 · Cited by 563
Life on the inside: the intracellular lifestyle of cytosolic bacteria
Ray, K., Marteyn, B., Sansonetti, P. J., & Tang, C. M. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2112 · Cited by 423
Chae, J. J., Komarow, H. D., Cheng, J., Wood, G., Raben, N., Liu, P. P., & Kastner, D. L. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00056-x · Cited by 412
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
Checroun, C., Wehrly, T. D., Fischer, E. R., Hayes, S. F., & Celli, J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601838103 · Cited by 356
Cryopyrin and pyrin activate caspase-1, but not NF-κB, via ASC oligomerization
Yu, J., Wu, J., Zhang, Z., Datta, P., Ibrahimi, I., Taniguchi, S., Sagara, J., Fernandes‐Alnemri, T., & Alnemri, E. S. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401734 · Cited by 350
Self-citationClemens, D. L., Lee, B., & Horwitz, M. A. (2004) · Infection and Immunity · doi:10.1128/iai.72.6.3204-3217.2004 · Cited by 349
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
Papin, S., Cuenin, S., Agostini, L., Martinon, F., Werner, S., Beer, H., Grütter, C., Grütter, M. G., & Tschopp, J. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402142 · Cited by 313
Pyrin Activates the ASC Pyroptosome in Response to Engagement by Autoinflammatory PSTPIP1 Mutants
Yu, J., Fernandes‐Alnemri, T., Datta, P., Wu, J., Juliana, C. A., Solórzano, L., McCormick, M., Zhang, Z., & Alnemri, E. S. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.08.029 · Cited by 288
Self-citationŠantić, M., Molmeret, M., Klose, K. E., Jones, S. C., & Kwaik, Y. A. (2005) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00526.x · Cited by 237
A public gene trap resource for mouse functional genomics
Skarnes, W. C., Nord, A. S., Cox, T., von Melchner, H., Wurst, W., Hicks, G. G., Young, S. G., Conklin, B. R., Ruiz, P., Soriano, P. M., et al. (2004) · Nature Genetics · doi:10.1038/ng0604-543 · Cited by 208
Chong, A., Wehrly, T. D., Nair, V., Fischer, E. R., Barker, J. R., Klose, K. E., & Celli, J. (2008) · Infection and Immunity · doi:10.1128/iai.00682-08 · Cited by 164
NLR-mediated control of inflammasome assembly in the host response against bacterial pathogens
Brodsky, I. E., & Monack, D. M. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.05.007 · Cited by 132
Toll-Like Receptor 2 Is Required for Inflammatory Responses to Francisella tularensis LVS
Katz, J., Zhang, P., Martin, M. H., Vogel, S., & Michalek, S. (2006) · Infection and Immunity · doi:10.1128/iai.74.5.2809-2816.2006 · Cited by 131
Toll-Like Receptor 2 Is Required for Control of Pulmonary Infection with Francisella tularensis
Malik, M., Bakshi, C. S., Sahay, B., Shah, A., Lotz, S. A., & Sellati, T. (2006) · Infection and Immunity · doi:10.1128/iai.02030-05 · Cited by 126
Šantić, M., Asare, R., Škrobonja, I., Jones, S. C., & Kwaik, Y. A. (2008) · Infection and Immunity · doi:10.1128/iai.00185-08 · Cited by 116
Henry, T., & Monack, D. M. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.01022.x · Cited by 90
Pyrin Critical to Macrophage IL-1β Response to Francisella Challenge
Gavrilin, M. A., Mitra, S., Seshadri, S., Nateri, J., Berhe, F., Hall, M. W., & Wewers, M. D. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803073 · Cited by 88
Francisella tularensis Phagosomal Escape Does Not Require Acidification of the Phagosome
Clemens, D. L., Lee, B., & Horwitz, M. A. (2009) · Infection and Immunity · doi:10.1128/iai.01485-08 · Cited by 74
Chapter Thirteen Assembly, Purification, and Assay of the Activity of the ASC Pyroptosome
Fernandes‐Alnemri, T., & Alnemri, E. S. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(08)01413-4 · Cited by 69
Self-citationTLR–Dependent Control of Francisella tularensis Infection and Host Inflammatory Responses
Abplanalp, A., Morris, I. R., Parida, B. K., Teale, J., & Berton, M. T. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007920 · Cited by 65
Bactericidal Activity of Alveolar Macrophages is Suppressed by V-ATPase Inhibition
Bidani, A., Reisner, B. S., Haque, A. K., Wen, J. J., Helmer, R. E., TUAZON, D. M., & Heming, T. A. (2000) · Lung · doi:10.1007/s004080000012 · Cited by 58
Frankenberg, T., Kirschnek, S., Häcker, H., & Häcker, G. A. (2007) · European Journal of Immunology · doi:10.1002/eji.200737379 · Cited by 50
International Gene Trap Project: Towards Gene-driven Saturation Mutagenesis in Mice
Araki, M., Araki, K., & Yamamura, K. (2009) · Current Pharmaceutical Biotechnology · doi:10.2174/138920109787315006 · Cited by 27
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Metadata
- Authors
- Fernandes-Alnemri, T., Yu, J.-W., Juliana, C., Solorzano, L., Kang, S., Wu, J., Datta, P., McCormick, M., Huang, L., McDermott, E., Eisenlohr, L., Landel, C. P., & Alnemri, E. S.
- Affiliations
- Thomas Jefferson University (US)
- Corresponding author
- Alnemri, Emad S
- Venue
- Nature Immunology
- Published
- 2010-03-28
- Volume
- 11
- Issue
- 5
- Pages
- 385-393
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC3111085
- OpenAlex
- W2157305255
- Cited by
- 732
- References
- 45
- Citations by year
- 2026: 26 · 2025: 19 · 2024: 34 · 2023: 22 · 2022: 25 · 2021: 35 · 2020: 30 · 2019: 39 · 2018: 42 · 2017: 60 · 2016: 53 · 2015: 57 · 2014: 58 · 2013: 73 · 2012: 51
- FWCI
- 29.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- YUHSpace (Yonsei University Medical Library) (submittedVersion, cc-by-nc-nd)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Harvard University
- National Institutes of Health
- National Institute on Aging (AG14357, R01AG014357)
- National Cancer Institute (T32 CA09678, T32CA009678)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR-055398, R01AR055398)
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacillus and Francisella bacterial research
- Keywords
- AIM2 inflammasome, Francisella tularensis, tularemia, innate immunity, macrophages, cytosolic DNA sensing, caspase-1 activation, IL-1β, IL-18, intracellular bacterial infection, host defense
- MeSH terms
- Animals, Cells, Cultured, DNA-Binding Proteins, Francisella tularensis, Humans, Immunity, Innate, Interferon Type I, L-Lactate Dehydrogenase, Macrophages, Nuclear Proteins, Tularemia, Mice, Knockout, Calcium Signaling, Caspase 1, Multiprotein Complexes, Interferon Regulatory Factor-3, Mice, Interleukin-1beta, Protein Multimerization
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