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代谢重编程:Th17细胞可塑性和异质性的新主宰

Metabolic rewiring: a new master of Th17 cell plasticity and heterogeneity.

作者信息

Papadopoulou Gina, Xanthou Georgina

机构信息

Cellular Immunology Laboratory, Center for Basic Research, Biomedical Research Foundation of the Academy of Athens, Greece.

Department of Genetics, Development and Molecular Biology, School of Biology, Aristotle University of Thessaloniki, Greece.

出版信息

FEBS J. 2022 May;289(9):2448-2466. doi: 10.1111/febs.15853. Epub 2021 Apr 12.

Abstract

T helper type 17 (Th17) cells are characterized by inherent plasticity and heterogeneity displaying both pathogenic and tissue-protective functions. Emerging evidence has illuminated a pivotal role for metabolic reprogramming in shaping Th17 cell fate determination. Metabolic responses are regulated by a constellation of factors and environmental triggers, including cytokines, nutrients, oxygen levels, and metabolites. Dysregulation of metabolic pathways not only influences Th17 cell plasticity and effector function but also affects the outcome of Th17-linked autoimmune, inflammatory, and antitumor responses. Understanding the molecular mechanisms underpinning metabolic reprogramming can allow the enhancement of protective Th17 cell-mediated responses during infections and cancer, concomitant with the suppression of detrimental Th17 processes during autoimmune and inflammatory diseases. In the present review, we describe major metabolic pathways underlying the differentiation of Th17 cells and their crosstalk with intracellular signaling mediators, we discuss how metabolic reprogramming affects Th17 cell plasticity and functions, and, finally, we outline current advances in the exploitation of metabolic checkpoints for the development of novel therapeutic interventions for the management of tissue inflammation, autoimmune disorders, and cancer.

摘要

17型辅助性T细胞(Th17细胞)具有固有的可塑性和异质性,兼具致病和组织保护功能。新出现的证据表明,代谢重编程在决定Th17细胞命运方面起着关键作用。代谢反应受一系列因素和环境触发因素调节,包括细胞因子、营养物质、氧水平和代谢产物。代谢途径的失调不仅影响Th17细胞的可塑性和效应功能,还会影响与Th17相关的自身免疫、炎症和抗肿瘤反应的结果。了解代谢重编程的分子机制有助于在感染和癌症期间增强保护性Th17细胞介导的反应,同时抑制自身免疫和炎症性疾病期间有害的Th17过程。在本综述中,我们描述了Th17细胞分化的主要代谢途径及其与细胞内信号介质的相互作用,讨论了代谢重编程如何影响Th17细胞的可塑性和功能,最后,我们概述了利用代谢检查点开发新型治疗干预措施以管理组织炎症、自身免疫性疾病和癌症方面的当前进展。

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