Metabolic pathways in T cell activation and lineage differentiation

被引:338
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
相关论文
共 141 条
[1]   CD28-mediated co-stimulation: A quantitative support for TCR signalling [J].
Acuto, O ;
Michel, F .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (12) :939-951
[2]  
Alberts B., 2002, THE MITOCHONDRION
[3]   AMPK in Lymphocyte Metabolism and Function [J].
Andris, Fabienne ;
Leo, Oberdan .
INTERNATIONAL REVIEWS OF IMMUNOLOGY, 2015, 34 (01) :67-81
[4]  
Andrzejewski S, 2014, CANCER METAB, V2, DOI 10.1186/2049-3002-2-12
[5]   Mammalian Target of Rapamycin Complex 1 (mTORC1) Enhances Bortezomib-induced Death in Tuberous Sclerosis Complex (TSC)-null Cells by a c-MYC-dependent Induction of the Unfolded Protein Response [J].
Babcock, Justin T. ;
Nguyen, Hoa B. ;
He, Yujun ;
Hendricks, Jeremiah W. ;
Wek, Ronald C. ;
Quilliam, Lawrence A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (22) :15687-15698
[6]   AMPK agonist downregulates innate and adaptive immune responses in TNBS-induced murine acute and relapsing colitis [J].
Bai, Aiping ;
Ma, Allan G. ;
Yong, Michael ;
Weiss, Carolyn R. ;
Ma, Yanbing ;
Guan, Qingdong ;
Bernstein, Charles N. ;
Peng, Zhikang .
BIOCHEMICAL PHARMACOLOGY, 2010, 80 (11) :1708-1717
[7]   Novel Anti-Inflammatory Action of 5-Aminoimidazole-4-carboxamide Ribonucleoside with Protective Effect in Dextran Sulfate Sodium-Induced Acute and Chronic Colitis [J].
Bai, Aiping ;
Yong, Michael ;
Ma, Allan G. ;
Ma, Yanbing ;
Weiss, Carolyn R. ;
Guan, Qingdong ;
Bernstein, Charles N. ;
Peng, Zhikang .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2010, 333 (03) :717-725
[8]   The Regulation of the Oxidative Phase of the Pentose Phosphate Pathway: New Answers to Old Problems [J].
Barcia-Vieitez, Ramiro ;
Ignacio Ramos-Martinez, Juan .
IUBMB LIFE, 2014, 66 (11) :775-779
[9]  
Baroja-Mazo Alberto, 2016, World J Transplant, V6, P183, DOI 10.5500/wjt.v6.i1.183
[10]   Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells [J].
Battaglia, M ;
Stabilini, A ;
Roncarolo, MG .
BLOOD, 2005, 105 (12) :4743-4748