The AIM2 inflammasome is essential for host defense against cytosolic bacteria and DNA viruses

被引:1051
作者
Rathinam, Vijay A. K. [1 ]
Jiang, Zhaozhao [1 ]
Waggoner, Stephen N. [2 ]
Sharma, Shruti [1 ]
Cole, Leah E. [3 ]
Waggoner, Lisa [1 ]
Vanaja, Sivapriya Kailasan [4 ]
Monks, Brian G. [1 ]
Ganesan, Sandhya [1 ]
Latz, Eicke [1 ,5 ]
Hornung, Veit [5 ]
Vogel, Stefanie N. [3 ]
Szomolanyi-Tsuda, Eva [2 ]
Fitzgerald, Katherine A. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Med, Div Infect Dis & Immunol, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01605 USA
[3] Univ Maryland, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
[4] Univ Massachusetts, Sch Med, Dept Mol Genet & Microbiol, Worcester, MA 01655 USA
[5] Univ Bonn, Inst Clin Chem & Pharmacol, D-5300 Bonn, Germany
基金
美国国家卫生研究院;
关键词
TOLL-LIKE RECEPTOR; FRANCISELLA-TULARENSIS; MURINE CYTOMEGALOVIRUS; VACCINIA VIRUS; INNATE; ACTIVATION; INFECTION; CASPASE-1; INTERLEUKIN-1; RECOGNITION;
D O I
10.1038/ni.1864
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammasomes regulate the activity of caspase-1 and the maturation of interleukin 1. (IL-1.) 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-1. 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-., 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.
引用
收藏
页码:395 / 403
页数:9
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