mTOR signalling and metabolic regulation of T cell differentiation

被引:71
|
作者
Peter, Christian [1 ]
Waldmann, Herman [1 ]
Cobbold, Stephen P. [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国医学研究理事会;
关键词
ACTIVATED PROTEIN-KINASE; AMINO-ACID TRANSPORTERS; FOXP3; EXPRESSION; RAG GTPASES; AKT-MTOR; RAPAMYCIN; MEMORY; EFFECTOR; CONSUMPTION; INDUCTION;
D O I
10.1016/j.coi.2010.08.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cells constantly monitor energy status and nutrient levels in order to adjust metabolic pathways according to their nutritional status and other environmental stimuli It is increasingly evident that the regulation of cellular metabolism is tightly coupled to T cell differentiation that ultimately determines the cellular fate The mammalian target of Rapamycin (mTOR) pathway has emerged as a key player in sensing these nutritional/energetic signals and in addition acts as a major integrator of growth factor induced signals so placing mTOR at the core of a signalling network controlling metabolism and cellular fate The mTOR pathway has been shown to play an important role in determining the differentiation of CD4(+) T cells into inflammatory and regulatory subsets in the induction of anergy in the development of CD8(+) memory T cells and the regulation of T cell trafficking
引用
收藏
页码:655 / 661
页数:7
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