Key roles of autophagy in regulating T-cell function

被引:60
作者
Botbol, Yair [1 ]
Guerrero-Ros, Ignacio [1 ]
Macian, Fernando [1 ]
机构
[1] Albert Einstein Coll Med, Dept Pathol, 1300 Morris Pk Ave, Bronx, NY 10467 USA
基金
美国国家卫生研究院;
关键词
Autophagy; Chaperone-mediated autophagy; Macroautophagy; Metabolism; T cell; CHAPERONE-MEDIATED AUTOPHAGY; SELECTIVE DEGRADATION; CYTOSOLIC PROTEINS; MAMMALIAN-CELLS; KINASE VPS34; ACTIVATION; SURVIVAL; MACROAUTOPHAGY; MEMBRANE; RECEPTOR;
D O I
10.1002/eji.201545955
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the past 10 years, autophagy has emerged as a crucial regulator of T-cell homeostasis, activation, and differentiation. Through the ability to adjust the cell's proteome in response to different stimuli, different forms of autophagy have been shown to control T-cell homeostasis and survival. Autophagic processes can also determine the magnitude of the T-cell response to TCR engagement, by regulating the cellular levels of specific signaling intermediates and modulating the metabolic output in activated T cells. In this review we will examine the mechanisms that control autophagy activity in T cells, such as ROS signaling and signaling through common gamma-chain cytokine receptors, and the different aspect of T-cell biology, including T-cell survival, effector cell function, and generation of memory, which can be regulated by autophagy.
引用
收藏
页码:1326 / 1334
页数:9
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