The JNK and P38 map kinase signaling pathways in T cell-mediated immune responses

被引:147
作者
Rincón, M
Flavell, RA
Davis, RA
机构
[1] Univ Vermont, Dept Med, Program Immunol, Burlington, VT 05405 USA
[2] Univ Massachusetts, Sch Med, Dept Biochem, Program Mol Med, Worcester, MA 01655 USA
[3] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, Sect Immunobiol,Dept Immunobiol, New Haven, CT 06510 USA
关键词
free radical; MAP kinases; T cells; thymocytes; P38; JNK; cytokines; NFAT;
D O I
10.1016/S0891-5849(00)00219-7
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
The mitogen-activated protein (MAP) kinase family members, which include the extracellular response kinases (ERK), p38, and c-Jun amino terminal kinases (JNK), play a role in mediating signals triggered by cytokines, growth factors, and environmental stress. JNK and p38 MAP kinases have been involved in inflammatory processes induced by a variety of stimuli, such as oxidative stress. Here, we describe the role of the JNK and p38 MAP kinase signaling pathways in the development of T cells in the thymus, and activation and differentiation of T cells in the peripheral immune system. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:1328 / 1337
页数:10
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