Metabolism and epigenetics at the heart of T cell function

被引:40
作者
Soriano-Baguet, Leticia [1 ,2 ]
Brenner, Dirk [1 ,2 ,3 ,4 ]
机构
[1] Luxembourg Inst Hlth, Dept Infect & Immun, Expt & Mol Immunol, Esch Sur Alzette, Luxembourg
[2] Univ Luxembourg, Luxembourg Ctr Syst Biomed, Immunol & Genet, Esch Sur Alzette, Luxembourg
[3] Univ Southern Denmark, Odense Univ Hosp, Odense Res Ctr Anaphylaxis, Dept Dermatol, Odense, Denmark
[4] Univ Southern Denmark, Odense Univ Hosp, Allergy Ctr, Odense, Denmark
关键词
BETA-HYDROXYBUTYRATE; TRANSCRIPTION FACTOR; EFFECTOR FUNCTION; LACTIC-ACID; DIFFERENTIATION; EXPRESSION; ACETYLATION; SERINE; ACTIVATION; IMMUNITY;
D O I
10.1016/j.it.2023.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell subsets adapt and rewire their metabolism according to their functions and surrounding microenvironment. Whereas naive T cells rely on mitochondrial metabolic pathways characterized by low nutrient requirements, effector T cells induce kinetically faster pathways to generate the biomass and energy needed for proliferation and cytokine production. Recent findings support the concept that alterations in metabolism also affect the epigenetics of T cells. In this review we discuss the connections between T cell metabolism and epigenetic changes such as histone post-translational modifications (PTMs) and DNA methylation, as well as the 'extra-metabolic' roles of metabolic enzymes and molecules. These findings collectively point to a new group of potential therapeutic targets for the treatment of T cell-dependent autoimmune diseases and cancers.
引用
收藏
页码:231 / 244
页数:14
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