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• W4313335857 endingPage "2591" @default.
• W4313335857 startingPage "2586" @default.
• W4313335857 abstract "Abstract Engagement of the TCR determines the fate of T cells to activate their functional programs, proliferate, or undergo apoptosis. The intracellular signal transduction pathways that dictate the specific outcome of receptor engagement have only been partially elucidated. The adapter protein, Shc, is involved in cytokine production, mitogenesis, transformation, and apoptosis in different cell systems. We found that Shc becomes phosphorylated on tyrosine residues upon stimulation of the TCR in DO11.10 hybridoma T cells; therefore, we investigated the role of Shc in activation-induced cell death in these cells by creating a series of stably transfected cell lines. Expression of Shc-SH2 (the SH2 domain of Shc) or Shc-Y239/240F (full-length Shc in which tyrosines 239 and 240 have been mutated to phenylalanine) resulted in the inhibition of activation-induced cell death and Fas ligand up-regulation after TCR cross-linking. Expression of wild-type Shc or Shc-Y317F had no significant effect. In addition, we found that Shc-SH2 and Shc-Y239/240F, but not Shc-Y317F, inhibited phosphorylation of extracellular signal-regulated protein kinase and production of IL-2 after TCR cross-linking. These results indicate an important role for Shc in the early signaling events that lead to activation-induced cell death and IL-2 production after TCR activation." @default.
• W4313335857 created "2023-01-06" @default.
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• W4313335857 date "1999-09-01" @default.
• W4313335857 modified "2023-10-12" @default.
• W4313335857 title "Requirement for Shc in TCR-Mediated Activation of a T Cell Hybridoma" @default.
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• W4313335857 doi "https://doi.org/10.4049/jimmunol.163.5.2586" @default.
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