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MAPK/ERK signaling in activated T cells inhibits CD95/Fas-mediated apoptosis downstream of DISC assembly
被引:167
作者:
Holmström, TH
Schmitz, I
Söderström, TS
Poukkula, M
Johnson, VL
Chow, SC
Krammer, PH
Eriksson, JE
机构:
[1] Univ Turku, Turku Ctr Biotechnol, FIN-20521 Turku, Finland
[2] Abo Akad Univ, FIN-20521 Turku, Finland
[3] Univ Turku, Turku Grad Sch Biomed Sci, FIN-20520 Turku, Finland
[4] Abo Akad Univ, Dept Biol, FIN-20520 Turku, Finland
[5] Univ Turku, Dept Biol, FIN-20014 Turku, Finland
[6] German Canc Res Ctr, Tumor Immunol Program, D-69120 Heidelberg, Germany
[7] Univ Leicester, Ctr Mech Human Tox, Leicester LE1 9HN, Leics, England
关键词:
apoptosis;
death receptor;
MAP kinase;
T cell activation;
T cell receptor;
D O I:
10.1093/emboj/19.20.5418
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
When T cells are activated, the expression of the CD95 ligand is elevated, with the purpose of inducing apoptosis in target cells and to later eliminate the activated T cells. We have shown previously that mitogen-activated protein kinase (MAPK or ERK) signaling suppresses CD95-mediated apoptosis in different cellular systems. In this study we examined whether MAPK signaling controls the persistence and CD95-mediated termination of an immune response in activated T cells. Our results show that activation of Jurkat T cells through the T cell receptor immediately suppresses CD95-mediated apoptosis, and that this suppression is mediated by MAPK activation. During the phase of elevated MAPK activity, the activation of caspase-8 and Bid is inhibited, whereas the assembly of a functional death-inducing signaling complex (DISC) is not affected. These results explain the resistance to CD95 responses observed during the early phase of T cell activation and suggest that MAPK-activation deflects DISC signaling from activating caspase-8 and Bid. The physiological relevance of the results was confirmed in activated primary peripheral T cells, in which inhibition of MAPK signaling markedly sensitized the cells to CD95-mediated apoptosis.
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页码:5418 / 5428
页数:11
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