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AIM2 activates the inflammasome and cell death in response to cytoplasmic DNA
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Host- and pathogen-associated cytoplasmic double-stranded DNA triggers the activation of a NALP3 (also known as cryopyrin and NLRP3)-independent inflammasome, which activates caspase-1 leading to maturation of pro-interleukin-1beta and inflammation. The nature of the cytoplasmic-DNA-sensing inflammasome is currently unknown. Here we show that AIM2 (absent in melanoma 2), an interferon-inducible HIN-200 family member that contains an amino-terminal pyrin domain and a carboxy-terminal oligonucleotide/oligosaccharide-binding domain, senses cytoplasmic DNA by means of its oligonucleotide/oligosaccharide-binding domain and interacts with ASC (apoptosis-associated speck-like protein containing a CARD) through its pyrin domain to activate caspase-1. The interaction of AIM2 with ASC also leads to the formation of the ASC pyroptosome, which induces pyroptotic cell death in cells containing caspase-1. Knockdown of AIM2 by short interfering RNA reduced inflammasome/pyroptosome activation by cytoplasmic DNA in human and mouse macrophages, whereas stable expression of AIM2 in the non-responsive human embryonic kidney 293T cell line conferred responsiveness to cytoplasmic DNA. Our results show that cytoplasmic DNA triggers formation of the AIM2 inflammasome by inducing AIM2 oligomerization. This study identifies AIM2 as an important inflammasome component that senses potentially dangerous cytoplasmic DNA, leading to activation of the ASC pyroptosome and caspase-1.
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“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 [49]
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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
Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica
Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658
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
Agostini, L., Martinon, F., Burns, K., McDermott, M. F., Hawkins, P. N., & Tschopp, J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00046-9 · Cited by 1,768
Crucial role for the Nalp3 inflammasome in the immunostimulatory properties of aluminium adjuvants
Eisenbarth, S. C., Colegio, O. R., O’Connor, W., Sutterwala, F. S., & Flavell, R. A. (2008) · Nature · doi:10.1038/nature06939 · Cited by 1,542
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 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
The inflammasome: a danger sensing complex triggering innate immunity
Pétrilli, V., Dostert, C., Muruve, D. A., & Tschopp, J. (2007) · Current Opinion in Immunology · doi:10.1016/j.coi.2007.09.002 · Cited by 700
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-citationFranchi, L., & Núñez, G. (2008) · European Journal of Immunology · doi:10.1002/eji.200838549 · Cited by 462
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Inflammasomes and autoimmune and rheumatic diseases: A comprehensive review
Shin, J. I., Lee, K. H., Joo, Y. H., Lee, J. M., Jeon, J., Jung, H. J., Shin, M., Cho, S., Kim, T.-H., Park, S., et al. (2019) · Journal of Autoimmunity · doi:10.1016/j.jaut.2019.06.010 · Cited by 125
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Gaidt, M. M., & Hornung, V. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.11.013 · Cited by 124
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Chen, R., Du, J., Zhu, H., & Ling, Q. (2021) · JHEP Reports · doi:10.1016/j.jhepr.2021.100324 · Cited by 131
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Barker, B. R., Taxman, D. J., & Ting, J. P. ‐. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.07.005 · Cited by 124
Innate Immune Cell Trafficking and Function During Sterile Inflammation of the Liver
McDonald, B., & Kubes, P. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.09.048 · Cited by 123
McFarlane, S., Aitken, J. D., Sutherland, J. S., Nicholl, M. J., Preston, V. G., & Preston, C. M. (2011) · Journal of Virology · doi:10.1128/jvi.02435-10 · Cited by 123
Gullett, J. M., Tweedell, R. E., & Kanneganti, T. (2022) · Cells · doi:10.3390/cells11091495 · Cited by 129
Ansari, M. A., Dutta, S., Veettil, M. V., Dutta, D., Iqbal, J., Kumar, B., Roy, A., Leela, C., Singh, V. V., & Chandran, B. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005019 · Cited by 123
Ge, J., Gong, Y., Xu, Y. X., & Shao, F. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117490109 · Cited by 132
Human NLRP3 inflammasome senses multiple types of bacterial RNAs
Sha, W., Mitoma, H., Hanabuchi, S., Bao, M., Weng, L., Sugimoto, N., Liu, Y., Zhang, Z., Zhong, J., Sun, B., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412487111 · Cited by 122
Konno, H., Yamamoto, T., Yamazaki, K., Gohda, J., Akiyama, T., Semba, K., Goto, H., Kato, A., Yujiri, T., Imai, T., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005674 · Cited by 122
Activation and Regulation of DNA-Driven Immune Responses
Paludan, S. R. (2015) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00061-14 · Cited by 128
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Stamm, C. E., Collins, A. C., & Shiloh, M. U. (2015) · Immunological Reviews · doi:10.1111/imr.12263 · Cited by 131
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Zhang, H., Luo, J., Alcorn, J. F., Chen, K., Fan, S., Pilewski, J. M., Liu, A., Chen, W., Kolls, J. K., & Wang, J. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1600714 · Cited by 122
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Jia, X., Yuan, S., Wang, Y., Fu, Y., Ge, Y., Ge, Y., Lan, X., Feng, Y., Qiu, F., Li, P., et al. (2017) · Nature Communications · doi:10.1038/ncomms14605 · Cited by 122
Hu, S., Peng, L., Kwak, Y.-T., McElvania, E., Pasare, C., Malter, J. S., Hooper, L. V., & Zaki, H. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.040 · Cited by 123
Ponomareva, L. V., Liu, H., Duan, X., Dickerson, E., Shen, H., Panchanathan, R., & Choubey, D. (2013) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-13-0145 · Cited by 120
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Gavrilin, M. A., Abdelaziz, D. H., Mostafa, M., Abdulrahman, B., Grandhi, J., Akhter, A., Khweek, A. A., Aubert, D., Valvano, M. A., Wewers, M. D., et al. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102272 · Cited by 123
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Vento‐Tormo, R., Rodríguez‐Ubreva, J., de la Rica, L., Urquiza, J., Javierre, B. M., Sabarinathan, R., Luque, A., Esteller, M., Aran, J. M., Álvarez‐Errico, D., et al. (2016) · Genome biology · doi:10.1186/s13059-015-0863-2 · Cited by 126
The immune system in cardiovascular diseases: from basic mechanisms to therapeutic implications
Wang, X., Chen, L., Wei, J., Zheng, H., Zhou, N., Xu, X., Deng, X., Liu, T., & Zou, Y. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02220-z · Cited by 132
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Sester, D. P., Thygesen, S. J., Sagulenko, V., Vajjhala, P. R., Cridland, J. A., Vitak, N., Chen, K. W., Osborne, G. W., Schroder, K., & Stacey, K. J. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1401110 · Cited by 119
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Nozaki, K., Li, L., & Miao, E. A. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101320-011235 · Cited by 121
Yasuda, K., Richez, C., Uccellini, M. B., Richards, R. J., Bonegio, R. G., Akira, S., Monestier, M., Corley, R. B., Viglianti, G. A., Marshak-Rothstein, A., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900399 · Cited by 118
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Bryan, N. B., Dorfleutner, A., Kramer, S. J., Yun, C., Rojanasakul, Y., & Stehlik, C. (2010) · Journal of Inflammation · doi:10.1186/1476-9255-7-23 · Cited by 123
Chattopadhyay, S., Yamashita, M., Zhang, Y., & Sen, G. C. (2011) · Journal of Virology · doi:10.1128/jvi.02133-10 · Cited by 117
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Inflammasomes as molecular mediators of inflammation and cancer: Potential role in melanoma
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Coutermarsh‐Ott, S. L., Eden, K. B., & Allen, I. C. (2016) · Journal of General Virology · doi:10.1099/jgv.0.000401 · Cited by 119
The essential adaptors of innate immune signaling
Chen, H., & Jiang, Z. (2012) · Protein & Cell · doi:10.1007/s13238-012-2063-0 · Cited by 116
Principles of inflammasome priming and inhibition: implications for psychiatric disorders
Herman, F. J., & Pasinetti, G. M. (2018) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2018.06.010 · Cited by 115
Sui, H., Zhou, M., Imamichi, H., Jiao, X., Sherman, B. T., Lane, H. C., & Imamichi, T. (2017) · Science Signaling · doi:10.1126/scisignal.aah5054 · Cited by 115
Gomes, M. T. R., Campos, P. C., Oliveira, F. S., Corsetti, P. P., Bortoluci, K. R., Cunha, L. D., Zamboni, D. S., & Oliveira, S. C. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202817 · Cited by 114
Lee, S. W., Vaccari, J. P. D. R., Truettner, J. S., Dietrich, W. D., & Keane, R. W. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1423-6 · Cited by 115
Vieyra-Garcia, P. A., & Wolf, P. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107784 · Cited by 114
Choubey, D., Duan, X., Dickerson, E., Ponomareva, L. V., Panchanathan, R., Shen, H., & Srivastava, R. (2010) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2009.0096 · Cited by 114
RNA Mediated toll-like receptor stimulation in health and disease
Dalpke, A. H., & Helm, M. (2012) · RNA Biology · doi:10.4161/rna.20206 · Cited by 113
Recognition of cytosolic DNA by c GAS and other STING ‐dependent sensors
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Tsuchiya, K., Hara, H., Kawamura, I., Nomura, T., Yamamoto, T., Daim, S. J., Dewamitta, S. R., Shen, Y., Fang, R., & Mitsuyama, M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001058 · Cited by 113
Kaminski, J. J., Schattgen, S. A., Tzeng, T.-C., Bode, C., Klinman, D. M., & Fitzgerald, K. A. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300530 · Cited by 112
Redox control of NLRP3 inflammasome activation in health and disease
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Nakanishi, A., Kaneko, N., Takeda, H., Sawasaki, T., Morikawa, S., Zhou, W., Kurata, M., Yamamoto, T., Akbar, S. M. F., Zako, T., et al. (2018) · Inflammation and Regeneration · doi:10.1186/s41232-018-0085-6 · Cited by 115
Licochalcone B specifically inhibits the NLRP3 inflammasome by disrupting NEK7‐NLRP3 interaction
Li, Q., Feng, H., Wang, H., Wang, Y., Mou, W., Xu, G., Zhang, P., Li, R., Shi, W., Wang, Z., et al. (2021) · EMBO Reports · doi:10.15252/embr.202153499 · Cited by 111
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Hu, M.-M., & Shu, H.-B. (2018) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100617-062903 · Cited by 110
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
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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
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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
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Shu, C., Li, X., & Li, P. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.06.006 · Cited by 110
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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
Zhang, M. Q., Zhao, Q., Xia, M., Chen, J., Chen, Y., Cao, X., Liu, Y., Yuan, Z., Wang, X., & Xu, Y. (2019) · The FASEB Journal · doi:10.1096/fj.201900394rrr · Cited by 101
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Gerlic, M., Faustin, B., Postigo, A. A., Yu, E. C.-W., Proell, M., Gombosuren, N., Krajewska, M., Flynn, R., Croft, M., Way, M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215995110 · Cited by 101
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Zahid, A., Ismail, H., Li, B., & Jin, T. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.613039 · Cited by 100
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Gorp, H. V., & Lamkanfi, M. (2019) · EMBO Reports · doi:10.15252/embr.201847575 · Cited by 101
Ketelut-Carneiro, N., Silva, G. K., Rocha, F. A., Milanezi, C. M., Neto, F. F. C., Zamboni, D. S., & Silva, J. S. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402321 · Cited by 100
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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Yang, M., Long, D., Hu, L., Zhao, Z., Li, Q., Guo, Y., He, Z., Zhao, M., Lu, L., Li, F., et al. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00725-x · Cited by 99
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PANoptosis in Viral Infection: The Missing Puzzle Piece in the Cell Death Field
Nguyen, L. N., & Kanneganti, T. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167249 · Cited by 100
Carta, S., Tassi, S., Pettinati, I., Delfino, L., Dinarello, C. A., & Rubartelli, A. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.203398 · Cited by 97
Ren, J., Wu, X., Jiang, R. M., Hao, D.-P., & Liu, Y. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.10.012 · Cited by 97
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Metadata
- Authors
- Fernandes-Alnemri, T., Yu, J.-W., Datta, P., Wu, J., & Alnemri, E. S.
- Affiliations
- Thomas Jefferson University (US)
- Corresponding author
- Alnemri, Emad S.
- Venue
- Nature
- Published
- 2009-01-21
- Volume
- 458
- Issue
- 7237
- Pages
- 509-513
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2862225
- OpenAlex
- W2042288276
- Cited by
- 1,831
- References
- 18
- Citations by year
- 2026: 56 · 2025: 78 · 2024: 96 · 2023: 108 · 2022: 110 · 2021: 101 · 2020: 102 · 2019: 112 · 2018: 114 · 2017: 111 · 2016: 105 · 2015: 109 · 2014: 92 · 2013: 126 · 2012: 100
- FWCI
- 54.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- YUHSpace (Yonsei University Medical Library) (submittedVersion, cc-by-nc-nd)
- The Medicine Forum (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (AG14357, R01AG014357)
- 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 › interferon and immune responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- AIM2, cytosolic DNA sensing, inflammasome, pyroptosis, caspase-1, ASC, pyrin domain, innate immunity, macrophages, NF-κB, IL-1β
- MeSH terms
- Animals, Cell Line, Cytoplasm, Cytoskeletal Proteins, DNA, DNA-Binding Proteins, Enzyme Activation, Humans, Inflammation, Nuclear Proteins, Protein Binding, Cell Death, Caspase 1, Apoptosis Regulatory Proteins, Mice, CARD Signaling Adaptor Proteins
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