The autoimmune suppressor Gadd45α inhibits the T cell alternative p38 activation pathway

被引:86
作者
Salvador, JM
Mittelstadt, PR
Belova, GI
Fornace, AJ
Ashwell, JD [1 ]
机构
[1] NCI, Lab Immune Cell Biol, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NCI, Gen Response Sect, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1038/ni1176
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The p38 MAP kinase ( MAPK) is phosphorylated and activated by upstream MAPK kinases. T cells have an alternative pathway in which T cell receptor - activated tyrosine kinase Zap70 phosphorylates p38 on Tyr323. Mice lacking Gadd45 alpha, a small p38-binding molecule, develop a lupus-like autoimmune disease. Here we show that resting T cells but not B cells from Gadd45a(-/-) mice had spontaneously increased p38 activity in the absence of 'upstream' MAPK kinase activation. The p38 from resting Gadd45a(-/-) T cells was spontaneously phosphorylated on Tyr323, and its activity was specifically inhibited by recombinant Gadd45a in vitro. Thus, constitutive activation of T cell p38 through the alternative pathway is prevented by Gadd45a, the absence of which results in p38 activation, T cell hyperproliferation and autoimmunity.
引用
收藏
页码:396 / 402
页数:7
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