共 21 条
Regulation of TLR4-mediated signaling by IBP/Def6, a novel activator of Rho GTPases
被引:22
作者:

Chen, Qinzhong
论文数: 0 引用数: 0
h-index: 0
机构:
Columbia Univ, Dept Med, New York, NY 10032 USA Columbia Univ, Dept Med, New York, NY 10032 USA

Gupta, Sanjay
论文数: 0 引用数: 0
h-index: 0
机构:
Columbia Univ, Dept Med, New York, NY 10032 USA Columbia Univ, Dept Med, New York, NY 10032 USA

Pernis, Alessandra B.
论文数: 0 引用数: 0
h-index: 0
机构:
Columbia Univ, Dept Med, New York, NY 10032 USA Columbia Univ, Dept Med, New York, NY 10032 USA
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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