Regulation and function of mTOR signalling in T cell fate decisions

被引:850
作者
Chi, Hongbo [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
HEMATOPOIETIC STEM-CELLS; ACTIVATED PROTEIN-KINASE; MAMMALIAN TARGET; ANTIGEN RECEPTOR; FOXP3; EXPRESSION; CLONAL EXPANSION; IMMUNE-RESPONSE; AMINO-ACIDS; RAPAMYCIN; DIFFERENTIATION;
D O I
10.1038/nri3198
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The evolutionarily conserved kinase mTOR (mammalian target of rapamycin) couples cell growth and metabolism to environmental inputs in eukaryotes. T cells depend on mTOR signalling to integrate immune signals and metabolic cues for their proper maintenance and activation. Under steady-state conditions, mTOR is actively controlled by multiple inhibitory mechanisms, and this enforces normal T cell homeostasis. Antigen recognition by naive CD4(+) and CD8(+) T cells triggers mTOR activation, which in turn programmes the differentiation of these cells into functionally distinct lineages. This Review focuses on the signalling mechanisms of mTOR in T cell homeostatic and functional fates, and discusses the therapeutic implications of targeting mTOR in T cells.
引用
收藏
页码:325 / 338
页数:14
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