期刊
CANCER LETTERS
卷 419, 期 -, 页码 20-26出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2018.01.033
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资金
- NIH [AI113919, AG031782, GM007288]
- Glenn Foundation for Medical Research
- Hirschl-Caulier Trust
- NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R56AI059738, R01AI113919] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007288] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE ON AGING [P01AG031782] Funding Source: NIH RePORTER
Autophagy, a highly conserved catabolic process that involves the degradation and recycling of intracellular components in the lysosome, has emerged as a key process in the maintenance of T cell homeostasis and the regulation of T cell differentiation and function. In this review, we provide an overview of the mechanisms that mediate the regulation of autophagy in T cells and discuss different cellular processes that are under the control of autophagy in CD4(+) and CD8(+) T cells. A special emphasis is placed on the role that autophagy plays in the modulation of T cell metabolism and the consequences of this regulation on functional states and programs of differentiation in specific T cell populations. (C) 2018 Elsevier B.V. All rights reserved.
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