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Sci. STKE, 5 April 2005 EDITORS' CHOICEIMMUNOLOGY A New Route to p38In a pair of back-to-back studies, Salvador et al. defined a new pathway to activation of the mitogen-activated protein kinase (MAPK) p38 in T cells and identified a suppressor of signaling through this pathway. MAPKs are activated in numerous cell types through a well-known cascade in which MAPK kinase kinases (MAPKKKs) activate MAPK kinases (MAPKKs), which activate MAPKs (see Rudd). Salvador et al. found that, in CD4+ T cells, T cell receptor (TCR) stimulation led to autophosphorylation of p38 MAPK through a process that did not require the conventional MAPK cascade. TCR-mediated phosphorylation of p38 did not depend on linker of activated T cells (LAT), although LAT was necessary for phosphorylation of the MAPKs ERK1/2 (extracellular signal-regulated kinase 1 and 2). The Src tyrosine kinase Lck was required for activation of p38, as was the tyrosine kinase Zap70. The TCR-mediated alternative pathway involved p38 phosphorylation on tyrosine 323 (Tyr323), leading to autophosphorylation of p38, as well as to phosphorylation of its substrates. Although Lck and Zap70 both phosphorylated p38 on Tyr323 in vitro, analysis of cells lacking Zap70 suggested that Zap70 acted downstream of Lck in p38 activation.
Gadd45 J. M. Salvador, P. R. Mittelstadt, T. Guszcynski, T. D. Copeland, H. Yamaguchi, E. Appella, A. J. Fornace Jr., J. D. Ashwell, Alternative p38 activation pathway mediated by T cell receptor-proximal tyrosine kinases. Nat. Immunol. 6, 390-395 (2005). [PubMed]
J. M. Salvador, P. R. Mittelstadt, G. I. Belova, A. J. Fornace Jr., J. D. Ashwell, The autoimmune suppressor Gadd45 C. E. Rudd, MAPK p38: Alternative and nonstressful in T cells. Nat. Immunol. 6, 368-370 (2005). [PubMed]
Citation: A New Route to p38. Sci. STKE 2005, tw123 (2005). The editors suggest the following Related Resources on Science sites:In Science Signaling
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Science Signaling. ISSN 1937-9145 (pre-2008: Science's STKE. ISSN 1525-8882)