Sci. STKE, 27 June 2000
Apoptosis Coactivation Leads to Survival
Integration of multiple signals can control whether cells live or die. Activation of the glucorticoid receptor (GR) or the T cell receptor (TCR)/CD3 complex can both cause apoptosis of T cells in certain circumstances. However, when these two receptors are activated simultaneously, glucocorticoid-induced apoptosis can be blocked. Jamieson and Yamamoto used pharmacological inhibitors and/or expression of pathway-specific mutant proteins to study the pathways mediating this cross talk between the TCR/CD3 complex and the glucocorticoid receptor. In both immortalized T cells lacking Fas and primary T cell cultures, activation of the Ras-Raf-mitogen-activated protein kinase pathway by the TCR/CD3 complex inhibited glucocorticoid-stimulated apoptosis, but did not involve the phosphatidylinositol 3 kinase and Akt pathway. Another pathway that provided protection was the pathway from Ras to activation of another GTP exchange factor, Ral.GDP. The authors found that activation of the TCR/CD3 complex did not regulate turnover of GR, but rather regulated (increased or decreased) the transcriptional activity of the receptors in a promoter-specific manner.
Jamieson, C.A.M., and Yamamoto, K.R. (2000) Crosstalk pathway for inhibition of glucocorticoid-induced apoptosis by T cell receptor signalling. Proc. Natl. Acad. Sci. U.S.A. 97: 7319-7324. [Abstract] [Full Text]
Citation: Coactivation Leads to Survival. Sci. STKE 2000, tw8 (2000).
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