| Literature DB >> 15735649 |
Jesus M Salvador1, Paul R Mittelstadt, Galina I Belova, Albert J Fornace, Jonathan D Ashwell.
Abstract
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 Gadd45alpha, 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 Gadd45alpha in vitro. Thus, constitutive activation of T cell p38 through the alternative pathway is prevented by Gadd45alpha, the absence of which results in p38 activation, T cell hyperproliferation and autoimmunity.Entities:
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Year: 2005 PMID: 15735649 DOI: 10.1038/ni1176
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606