Metabolic orchestration of T lineage differentiation and function.

Abstract:

:T cells are stimulated by the engagement of antigen, cytokine, pathogen, and hormone receptors. While research performed over many years has focused on deciphering the molecular components of these pathways, recent data underscore the importance of the metabolic environment in conditioning responses to receptor engagement. The ability of T cells to undergo a massive proliferation and cytokine secretion in response to receptor signals requires alterations to their bioenergetic homeostasis, allowing them to meet new energetic and biosynthetic demands. The metabolic reprogramming of activated T cells is regulated not only by changes in intracellular nutrient uptake and utilization but also by nutrient and oxygen concentrations in the extracellular environment. Notably, the extracellular environment can be profoundly altered by pathological conditions such as infections and tumors, thereby perturbing the metabolism and function of antigen-specific T lymphocytes. This review highlights the interplay between diverse metabolic networks and the transcriptional/epigenetic states that condition T-cell differentiation, comparing the metabolic features of T lymphocytes with other immune cells. We further address recent discoveries in the metabolic pathways that govern T-cell function in physiological and pathological conditions.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Yong CS,Abba Moussa D,Cretenet G,Kinet S,Dardalhon V,Taylor N

doi

10.1002/1873-3468.12849

subject

Has Abstract

pub_date

2017-10-01 00:00:00

pages

3104-3118

issue

19

eissn

0014-5793

issn

1873-3468

journal_volume

591

pub_type

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