Metabolic pathways in T cell activation and lineage differentiation

被引:326
作者
Almeida, Luis [1 ]
Lochner, Matthias [1 ]
Berod, Luciana [1 ]
Sparwasser, Tim [1 ]
机构
[1] TWINCORE, Ctr Expt & Clin Infect Res, Inst Infect Immunol, Hannover, Germany
关键词
T cells; Metabolism; Glycolysis; Fatty acid metabolism; mTOR; AMPK; ACC; FATTY-ACID-METABOLISM; REGULATORY T; PROTEIN-KINASE; TUMOR MICROENVIRONMENT; MAMMALIAN TARGET; TH17; CELLS; 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBONUCLEOSIDE; ORGAN-TRANSPLANTATION; AEROBIC GLYCOLYSIS; ENERGY-METABOLISM;
D O I
10.1016/j.smim.2016.10.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent advances in the field of immunometabolism support the concept that fundamental processes in T cell biology, such as TCR-mediated activation and T helper lineage differentiation, are closely linked to changes in the cellular metabolic programs. Although the major task of the intermediate metabolism is to provide the cell with a constant supply of energy and molecular precursors for the production of biomolecules, the dynamic regulation of metabolic pathways also plays an active role in shaping T cell responses. Key metabolic processes such as glycolysis, fatty acid and mitochondrial metabolism are now recognized as crucial players in T cell activation and differentiation, and their modulation can differentially affect the development of T helper cell lineages. In this review, we describe the diverse metabolic processes that T cells engage during their life cycle from nave towards effector and memory T cells. We consider in particular how the cellular metabolism may actively support the function of T cells in their different states. Moreover, we discuss how molecular regulators such as mTOR or AMPK link environmental changes to adaptations in the cellular metabolism and elucidate the consequences on T cell differentiation and function. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:514 / 524
页数:11
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