The transcription factor IRF1 and guanylate-binding proteins target activation of the AIM2 inflammasome by Francisella infection

被引:281
|
作者
Man, Si Ming [1 ,2 ]
Karki, Rajendra [1 ]
Malireddi, R. K. Subbarao [1 ]
Neale, Geoffrey [3 ]
Vogel, Peter [4 ,5 ]
Yamamoto, Masahiro [6 ]
Lamkanfi, Mohamed [7 ,8 ]
Kanneganti, Thirumala-Devi [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW, Australia
[3] St Jude Childrens Res Hosp, Hartwell Ctr Bioinformat & Biotechnol, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Anim Resources Ctr, Memphis, TN 38105 USA
[5] St Jude Childrens Res Hosp, Vet Pathol Core, Memphis, TN 38105 USA
[6] Osaka Univ, Dept Microbiol & Immunol, Osaka, Japan
[7] Vlaams Inst Biotechnol, Dept Med Prot Res, Ghent, Belgium
[8] Univ Ghent, Dept Biochem, B-9000 Ghent, Belgium
基金
欧洲研究理事会; 美国国家卫生研究院; 英国医学研究理事会;
关键词
INNATE IMMUNITY; HOST-DEFENSE; TULARENSIS; INDUCTION; NLRP3; TOLL; DISRUPTION; MECHANISMS; REGULATOR; CASPASE-1;
D O I
10.1038/ni.3118
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 are critical for mounting host defense against pathogens. The molecular mechanisms that control activation of the AIM2 inflammasome in response to different cytosolic pathogens remain unclear. Here we found that the transcription factor IRF1 was required for activation of the AIM2 inflammasome during infection with the Francisella tularensis subspecies novicida (F. novicida), whereas engagement of the AIM2 inflammasome by mouse cytomegalovirus (MCMV) or transfected double-stranded DNA did not require IRF1. Infection of F. novicida detected by the DNA sensor cGAS and its adaptor STING induced type I interferon-dependent expression of IRF1, which drove the expression of guanylate-binding proteins (GBPs); this led to intracellular killing of bacteria and DNA release. Our results reveal a specific requirement for IRF1 and GBPs in the liberation of DNA for sensing by AIM2 depending on the pathogen encountered by the cell.
引用
收藏
页码:467 / U174
页数:11
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