Autophagy in regulatory T cells: A double-edged sword in disease settings

被引:17
|
作者
Zhang, Jing [1 ]
Chen, Longmin [1 ]
Xiong, Fei [1 ]
Zhang, Shu [1 ]
Huang, Kun [3 ]
Zhang, Ziyun [1 ,2 ]
Wang, Cong-Yi [1 ]
机构
[1] Huazhong Univ Sci & Technol, Chinese Acad Med Sci, Key Lab Organ Transplantat,Ctr Biomed Res,Minist, NHC Key Lab Organ Transplantat,Key Lab Organ Tran, Wuhan 430030, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Rheumatol, 1095 Jiefang Ave, Wuhan 430030, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Sch Pharm, 1095 Jiefang Ave, Wuhan 430030, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Autophagy; Regulatory T cells; GVHD; Autoimmune disease; Tumor; Infectious disease; HEPATITIS-B-VIRUS; VERSUS-HOST-DISEASE; TRANSCRIPTION FACTOR FOXP3; GENOME-WIDE ASSOCIATION; ADAPTIVE IMMUNITY; EPIGENETIC CONTROL; CROHN-DISEASE; GENE ATG5; INNATE; DIFFERENTIATION;
D O I
10.1016/j.molimm.2019.02.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy is an evolutionarily conserved catabolic process that directs cytoplasmic proteins, organelles and microbes to lysosomes for degradation. It not only represents an essential cell-intrinsic mechanism to protect against internal and external stresses but also shapes both innate and adaptive immunity. Regulatory T cells (Tregs) are a developmentally and functionally distinct T cell subpopulation engaged in sustaining immunological self-tolerance and homeostasis. There is compelling evidence that autophagy is actively regulated in Tregs and serves as a central signal-dependent controller for Tregs by restraining excessive apoptotic and metabolic activities. In this review, we discuss how autophagy modulates the stability and functionality of Tregs in different disease settings, and provide a perspective on how manipulation of autophagy enables better control of immune response by targeting the generation of Tregs and the maintenance of their stability.
引用
收藏
页码:43 / 50
页数:8
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