Nuclear factor of activated T cells c is a target of p38 mitogen-activated protein kinase in T cells

被引:69
|
作者
Wu, CC
Hsu, SC
Shih, HM
Lai, MZ [1 ]
机构
[1] Acad Sinica, Inst Mol Biol, Taipei 11529, Taiwan
[2] Natl Taiwan Univ, Sch Med, Grad Inst Immunol, Taipei, Taiwan
[3] Natl Yang Ming Univ, Natl Hlth Res Inst, Div Mol & Genom Med, Taipei 112, Taiwan
[4] Natl Yang Ming Univ, Grad Inst Microbiol & Immunol, Taipei 112, Taiwan
关键词
D O I
10.1128/MCB.23.18.6442-6454.2003
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
p38 mitogen activated protein kinase (MAPK) is essential for T-cell activation. Here we demonstrated that nuclear factor of activated T cells (NFAT) is a direct target of p38 MAPK. Inhibition of p38 MAPK led to selective inactivation of NFAT in T cells. We further linked a strict requirement of p38 MAPK to activation of NFATc. A stimulatory effect of p38 MAPK on at least four other stages of NFATc activation was found. First, the p38 MAPK cascade activated the NFATc promoter and induced the transcription of NFATc mRNA. Second, p38 MAPK mildly increased the mRNA stability of NFATc. Third, p38 MAPK enhanced the translation of NFATc mRNA. Fourth, p38 MAPK promoted the interaction of NFATc with the coactivator CREB-binding protein. In contrast, p38 MAPK moderately enhanced the expulsion of NFATc from the nucleus in T cells. Therefore, p38 MAPK has opposite effects on different stages of NFATc activation. All together, the overall effect of p38 MAPK on NFATc in T cells is clear activation.
引用
收藏
页码:6442 / 6454
页数:13
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