Regulation of TLR4-mediated signaling by IBP/Def6, a novel activator of Rho GTPases

被引:22
作者
Chen, Qinzhong [1 ]
Gupta, Sanjay [1 ]
Pernis, Alessandra B. [1 ]
机构
[1] Columbia Univ, Dept Med, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
proinflammatory cytokines; MAPK; NF-kappa B; GEF; NUCLEOTIDE-EXCHANGE FACTOR; TOLL-LIKE RECEPTORS; INNATE IMMUNITY; NEGATIVE REGULATION; RESPONSES; SWAP-70; SYSTEM; LEADS; LPS; IBP;
D O I
10.1189/jlb.0308219
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
TLRs play a fundamental role in innate immune responses. Although Rho GTPases have been implicated in TLR-mediated signaling pathways, the molecules that control their activation in response to TLR engagement are largely unknown. IFN regulatory factor-4-binding protein (IBP; which is encoded by the gene Def6) is a unique type of activator for Rac that plays a crucial role in TCR-mediated signaling and adaptive immune responses. Here, we demonstrate that IBP/Def6 also controls innate immune responses by modulating TLR-induced signaling events. Mice deficient in IBP/Def6 are protected from LPS-induced septic shock. This protection is associated with a decrease in the production of proinflammatory cytokines and is accompanied by diminished activation of MAPKs and NF-kappa B. Our results thus identify IBP/Def6 as a novel component of the TLR4-induced signaling cascade that controls the production of proinflammatory cytokines. J. Leukoc. Biol. 85: 539-543; 2009.
引用
收藏
页码:539 / 543
页数:5
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