Caspase-1 activation of IL-1β and IL-18 are essential for Shigella flexneri-induced inflammation

被引:327
作者
Sansonetti, PJ
Phalipon, A
Arondel, J
Thirumalai, K
Banerjee, S
Akira, S
Takeda, K
Zychlinsky, A
机构
[1] NYU, Sch Med, Skirball Inst, Dept Microbiol, New York, NY 10016 USA
[2] NYU, Kaplan Canc Ctr, Sch Med, New York, NY 10016 USA
[3] BASF Biores Corp, Worcester, MA 01605 USA
[4] Osaka Univ, Res Inst Microbial Dis, Dept Host Def, Suita, Osaka 5650871, Japan
[5] Inst Pasteur, INSERM, Unite Pathogenie Microbienne Mol, U389, F-75724 Paris 15, France
关键词
D O I
10.1016/S1074-7613(00)80209-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Caspases are intracellular proteases that mediate mammalian cell apoptosis. Caspase-1 (Casp-1) is a unique caspase because it activates the proinflammatory cytokines interleukin (Il)-1 beta and IL-18. Shigella flexneri, the etiological agent of bacillary dysentery, induces macrophage apoptosis, which requires Casp-1 and results in the release of mature IL-1 beta and IL-18. Here we show that casp-1(-/-) mice infected with S. flexneri do not develop the acute inflammation characteristic of shigellosis and are unable to resolve the bacterial infection. Using casp-1(-/-) mice supplemented with recombinant cytokines and experiments with IL-1 beta(-/-) and IL-18(-/-) mice, we show that IL-1 beta and IL-18 are both required to mediate inflammation in S. flexneri infections. Together, these data demonstrate the importance of Casp-1 in acute inflammation and show the different roles of its substrates, IL-1 beta and IL-18, in this response.
引用
收藏
页码:581 / 590
页数:10
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