共 65 条
The Erk2 MAPK Regulates CD8 T Cell Proliferation and Survival
被引:153
作者:

D'Souza, Warren N.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA

Chang, Chiung-Fang
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA

Fischer, April M.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA

Li, Manqing
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA

Hedrick, Stephen M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA
机构:
[1] Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA
基金:
美国国家卫生研究院;
关键词:
D O I:
10.4049/jimmunol.181.11.7617
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The magnitude of T cell responses is determined by proliferation and survival decisions made by the responding cells. We now demonstrate that the Erk MAPK pathway plays a critical role in these cell fate decisions within CD8 T cells. While Erk1 is dispensable for all aspects of CD8 T cell activation, Erk2 is required for the proliferation or CD8 T cells activated in the absence of costimulation. Surprisingly, Erk2 is not required for proliferation following the addition of a costimulatory signal in vitro, or upon viral infection in vivo, but regulates the size of the responding population by enhancing cell survival. An important component or this Erk2-derived signal is the transcriptional regulation of Bcl-2 family members Bcl-x(L) and Bim, and impaired Erk2-deficient CD8 T cell survival can be rescued by genetic ablation or Bim. These studies ascribe multifaceted functions specific to Erk2 in CD8 T cell activation, proliferation, and survival. The Journal of Immunology, 2008, 181: 7617-7629.
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页码:7617 / 7629
页数:13
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