Salvador Jesus M, Mittelstadt Paul R, Guszczynski Tad, Copeland Terry D, Yamaguchi Hiroshi, Appella Ettore, Fornace Albert J, Ashwell Jonathan D
Gene Response Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Nat Immunol. 2005 Apr;6(4):390-5. doi: 10.1038/ni1177. Epub 2005 Feb 27.
Signaling-responsive MAP kinases (MAPKs) are key in mediating immune responses and are activated through the phosphorylation of a Thr-X-Tyr motif by upstream MAPK kinases. Here we show that T cells stimulated through the T cell receptor (TCR) used an alternative mechanism in which p38 was phosphorylated on Tyr323 and subsequently autophosphorylated residues Thr180 and Tyr182. This required the TCR-proximal tyrosine kinase Zap70 but not the adaptor protein LAT, which was required for activation of extracellular signal-regulated protein kinase MAPKs. TCR activation of p38 lacking Tyr323 was diminished, and blocking of p38 activity prevented p38 dual phosphorylation in normal T cells but not in B cells. Thus, phosphorylation of Tyr323 dependent on the tyrosine kinase Lck and mediated by Zap70 serves as an important mechanism for TCR activation of p38 in T cells.
信号响应性丝裂原活化蛋白激酶(MAPK)在介导免疫反应中起关键作用,并通过上游MAPK激酶对苏氨酸- X -酪氨酸基序的磷酸化而被激活。在此我们表明,通过T细胞受体(TCR)刺激的T细胞使用了一种替代机制,其中p38在酪氨酸323位点被磷酸化,随后苏氨酸180和酪氨酸182位点发生自身磷酸化。这需要TCR近端酪氨酸激酶Zap70,但不需要衔接蛋白LAT,而LAT是细胞外信号调节蛋白激酶MAPK激活所必需的。缺乏酪氨酸323的p38的TCR激活减弱,并且阻断p38活性可阻止正常T细胞中p38的双重磷酸化,但不能阻止B细胞中的这种磷酸化。因此,依赖酪氨酸激酶Lck并由Zap70介导的酪氨酸323磷酸化是T细胞中TCR激活p38的重要机制。