The Erk2 MAPK Regulates CD8 T Cell Proliferation and Survival

被引:153
作者
D'Souza, Warren N.
Chang, Chiung-Fang
Fischer, April M.
Li, Manqing
Hedrick, Stephen M. [1 ]
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.
引用
收藏
页码:7617 / 7629
页数:13
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