Protein kinase C epsilon: a new target to control inflammation and immune-mediated disorders

被引:73
作者
Aksoy, E [1 ]
Goldman, M [1 ]
Willems, F [1 ]
机构
[1] Free Univ Brussels, Expt Immunol Lab, B-1070 Brussels, Belgium
关键词
protein kinase C epsilon; innate immunity; IL-12; T-H; 1;
D O I
10.1016/S1357-2725(03)00210-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in understanding the molecular basis for mammalian host immune responses to microbial invasion suggest that the first line of defense against microbes is the recognition of pathogen-associated molecular patterns by a set of germline-encoded receptors: the Toll-like receptors (TLRs). TLRs have been identified as being part of a large family of pathogen-recognition receptors that play a decisive role in the induction of both innate and adaptive immunity. Indeed, activation of T lymphocytes depends on their interaction with dendritic cells previously stimulated by TLR agonists such as bacterial lipopolysaccharide (LPS), a TLR-4 ligand. A novel PKC epsilon (epsilon) was recently found to be a critical component of TLR-4 signaling pathway and thereby to play a key role in macrophage and dendritic cell (DC) activation in response to LPS. Thus, controlling the kinase activity of PKC epsilon might represent an efficient strategy to prevent or treat certain inflammatory disorders of microbial origin. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 188
页数:6
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