T cell dependence on mTOR signaling

被引:19
作者
Mills, Robyn E. [2 ]
Jameson, Julie M. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
关键词
T cell; signaling; skin; cell trafficking; cell proliferation; LYMPHOCYTE TRAFFICKING; MAMMALIAN TARGET; WOUND REPAIR; RAPAMYCIN; RICTOR; ACTIVATION; COMPLEX; PHOSPHORYLATION; CYTOSKELETON; AKT/PKB;
D O I
10.4161/cc.8.4.7625
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mammalian target of rapamycin (mTOR) signaling pathway integrates signals from the environment to the nucleus for the regulation of cellular growth, metabolism and survival. Lymphocytes frequently rely on this pathway, but it is carefully regulated through the reception of signals via cytokine, growth factor and co-stimulatory receptors. Recent studies have begun to elucidate why T cell subsets rely on this pathway to varying degrees. Ultimately these findings will help distinguish the parameters that guide T cell homeostasis and activation-induced function between the different T cell populations. The mTOR pathway has been the focus of many immunosuppressive and cancer treatment regimens, therefore there is a great need to understand the impact of suppression not only on the T cell populations targeted, but on bystander T cells as well.
引用
收藏
页码:545 / 548
页数:4
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