HIF1α and metabolic reprogramming in inflammation

被引:498
|
作者
Corcoran, Sarah E. [1 ]
O'Neill, Luke A. J. [1 ]
机构
[1] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Biochem & Immunol, Dublin, Ireland
来源
JOURNAL OF CLINICAL INVESTIGATION | 2016年 / 126卷 / 10期
基金
爱尔兰科学基金会; 英国惠康基金;
关键词
HYPOXIA-INDUCIBLE FACTOR; PYRUVATE-KINASE M2; KAPPA-B ACTIVITY; FACTOR-I; GENE-EXPRESSION; MACROPHAGE POLARIZATION; REGULATORY T; TRANSCRIPTIONAL REGULATION; MEDIATED INFLAMMATION; SIGNALING PATHWAY;
D O I
10.1172/JCI84431
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
HIF1 alpha is a common component of pathways involved in the control of cellular metabolism and has a role in regulating immune cell effector functions. Additionally, HIF1 alpha is critical for the maturation of dendritic cells and for the activation of T cells. HIF1 alpha is induced in LPS-activated macrophages, where it is critically involved in glycolysis and the induction of proinflammatory genes, notably II1b. The mechanism of LPS-stimulated HIF1 alpha induction involves succinate, which inhibits prolyl hydroxylases (PHDs). Pyruvate kinase M2 (PKM2) is also induced and interacts with and promotes the function of HIF1 alpha. In another critical inflammatory cell type, Th17 cells, HIF1 alpha acts via the retinoic acid-related orphan receptor-gamma t (ROR gamma t) to drive Th17 differentiation. HIF1 alpha is therefore a key reprogrammer of metabolism in inflammatory cells that promotes inflammatory gene expression.
引用
收藏
页码:3699 / 3707
页数:9
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