HIF-1 in the inflammatory microenvironment

被引:191
作者
Dehne, Nathalie [1 ]
Bruene, Bernhard [1 ]
机构
[1] Goethe Univ Frankfurt, ZAFES, Inst Biochem Pathobiochem 1, D-60590 Frankfurt, Germany
关键词
Neutrophils; NF-kappa B; NFAT; PHD; Cytokines; ROS; NO; HYPOXIA-INDUCIBLE FACTOR-1; NITRIC-OXIDE; UP-REGULATION; BACTERICIDAL CAPACITY; SIGNALING PATHWAY; INNATE IMMUNITY; FACTOR; 1-ALPHA; HIF-1-ALPHA; EXPRESSION; ACTIVATION;
D O I
10.1016/j.yexcr.2009.03.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia-inducible factor (HIF) is a transcriptional activator that coordinates adaptive responses to hypoxia. All increased activity is recognized in the majority of clinical relevant hypoxic/ischemic episodes and human cancers. However, studies with HIF-1 alpha knockout mice revealed all important role of HIF-1 lot physiology such as embryogenesis or glycolytic energy production. The discovery that HIF-1 activity is not only restricted to pathological conditions of reduced oxygen availability but also is needed for the normal O-2-homeostasis by regulating O-2-delivery and consumption opens a diverse spectrum of so far unappreciated HIF-1 functions in several organs, including the immune system. Innate immune responses are orchestrated by macrophages. These cells respond to environmental input signals and ill turn generate appropriate answers to initiate resolution Of inflammation. It appears that multiple pathways in the inflammatory microenvironment are Used to adjust HIF-1 a levels to affect macrophage biology. This review summarizes mechanisms of HIF activation in mammalian immune cells, especially in macrophages and neutrophils, and outlines how HIF moderates inflammation. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1791 / 1797
页数:7
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