Regulation of JNK and p38 MAPK in the immune system: Signal integration, propagation and termination

被引:278
作者
Huang, Gonghua [1 ]
Shi, Lewis Zhichang [1 ]
Chi, Hongbo [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
Kinase; Phosphatase; Signaling; Receptor; Immunity; NF-KAPPA-B; ACTIVATED PROTEIN-KINASE; TOLL-LIKE-RECEPTOR; PROINFLAMMATORY CYTOKINE BIOSYNTHESIS; STRESS-INDUCED PHOSPHORYLATION; C-JUN; PHOSPHATASE-1; DEGRADATION; DIFFERENTIAL REGULATION; INFLAMMATORY SIGNALS; MEDIATED ACTIVATION;
D O I
10.1016/j.cyto.2009.08.002
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
Stress-activated MAP kinases (MAPKs), comprised of JNK and p38, play prominent roles in the innate and adaptive immune systems. Activation of MAPKs is mediated by a three-tiered kinase module comprised of MAPK kinase kinases (MAP3Ks), MAPK kinases (MAP2Ks) and MAPKs through sequential protein phosphorylation. Activated MAPKs, in turn, phosphorylate transcription factors and other targets to regulate gene transcription and immune responses. Recent studies have provided new insight into the upstream and downstream components of the MAPK pathway that facilitate the activation and propagation of MAPK signaling in immune responses. Moreover, MAPK activity is negatively regulated by MAPK phosphatases (MKPs), a group of dual-specificity phosphatases that dephosphorylate and inactivate the MAPKs. Here we discuss the recent advances in our understanding of these regulatory processes in MAPK signaling with a focus on their impacts on immune function. (C) 2009 Elsevier Ltd. All rights reserved
引用
收藏
页码:161 / 169
页数:9
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