Rethinking the paradigm: How comparative studies on fatty acid oxidation inform our understanding of T cell metabolism

被引:11
作者
Chiaranunt, Pailin [1 ]
Ferrara, James L. M. [2 ,3 ]
Byersdorfer, Craig A. [1 ]
机构
[1] Univ Pittsburgh, Div Blood & Marrow Transplant & Cellular Therapie, Dept Pediat, Sch Med, Pittsburgh, PA 15224 USA
[2] Icahn Sch Med, Tisch Canc Inst, Hess Ctr Sci & Med, New York, NY 10029 USA
[3] Icahn Sch Med, Div Hematol Med Oncol, Hess Ctr Sci & Med, New York, NY 10029 USA
关键词
T-cell metabolism; Graft-versus-host disease; Fatty acid oxidation; Oxidative phosphorylation; PROLIFERATOR-ACTIVATED RECEPTOR; PENTOSE-PHOSPHATE PATHWAY; ENERGY-METABOLISM; PROTEIN-KINASE; MITOCHONDRIAL BIOGENESIS; SKELETAL-MUSCLE; PPAR-ALPHA; ACETYL-COENZYME; GENE-EXPRESSION; SIRTUIN;
D O I
10.1016/j.molimm.2015.07.023
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
The classic paradigm of T cell metabolism posits that activated T-eff cells utilize glycolysis to keep pace with increased energetic demands, while resting and T-mem cells rely on the oxidation of fat. In contrast, T-eff cells during graft-versus-host disease (GVHD) increase their reliance on oxidative metabolism and, in particular, on fatty acid oxidation (FAO). To explore the potential mechanisms driving adoption of this alternative metabolism, we first review key pathways regulating FAO across a variety of disparate tissue types, including liver, heart, and skeletal muscle. Based upon these comparative studies, we then outline a consensus network of transcriptional and signaling pathways that predict a model for regulating FAO in T-eff cells during GVHD. This model raises important implications about the dynamic nature of metabolic reprogramming in T cells and suggests exciting future directions for further study of in vivo T cell metabolism. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:564 / 574
页数:11
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