Metabolic Controls on Epigenetic Reprogramming in Regulatory T Cells

被引:16
作者
Lu, Jingli [1 ,2 ,3 ]
Liang, Yan [1 ,2 ,3 ]
Meng, Haiyang [1 ,2 ,3 ]
Zhang, Ailing [1 ,2 ,3 ]
Zhao, Junjie [1 ,2 ,3 ]
Zhang, Chengliang [4 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Pharm, Zhengzhou, Peoples R China
[2] Henan Engn Res Ctr Clin Mass Spectrometry Precis, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Zhengzhou Key Lab Clin Mass Spectrometry, Zhengzhou, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Pharm, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
regulatory T cells; metabolism; epigenetics; immune suppression; metabolites; PROTEIN O-GLCNACYLATION; FOXP3; EXPRESSION; DNA-METHYLATION; TRANSCRIPTION FACTOR; MITOCHONDRIAL BIOGENESIS; BETA-HYDROXYBUTYRATE; CELLULAR-METABOLISM; ACETYL-COENZYME; KEY DETERMINANT; HISTONE;
D O I
10.3389/fimmu.2021.728783
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Forkhead box protein 3 (Foxp3(+))-expressing regulatory T (Treg) cells are a unique CD4(+)T cell subset that suppresses excessive immune responses. The epigenetic plasticity and metabolic traits of Treg cells are crucial for the acquisition of their phenotypic and functional characteristics. Therefore, alterations to the epigenetics and metabolism affect Treg cell development and function. Recent evidence reveals that altering the metabolic pathways and generation of metabolites can regulate the epigenetics of Treg cells. Specifically, some intermediates of cell metabolism can directly act as substrates or cofactors of epigenetic-modifying enzymes. Here, we describe the metabolic and epigenetic features during Treg cell development, and discuss how metabolites can contribute to epigenetic alterations of Treg cells, which affects Treg cell activation, differentiation, and function.
引用
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页数:13
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