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炎症微环境中的缺氧诱导因子-1

HIF-1 in the inflammatory microenvironment.

作者信息

Dehne Nathalie, Brüne Bernhard

机构信息

Institute of Biochemistry I-Pathobiochemistry/ZAFES, Goethe-University, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.

出版信息

Exp Cell Res. 2009 Jul 1;315(11):1791-7. doi: 10.1016/j.yexcr.2009.03.019. Epub 2009 Mar 28.

Abstract

Hypoxia-inducible factor (HIF) is a transcriptional activator that coordinates adaptive responses to hypoxia. An increased activity is recognized in the majority of clinical relevant hypoxic/ischemic episodes and human cancers. However, studies with HIF-1alpha knockout mice revealed an important role of HIF-1 for 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 O2-homeostasis by regulating O2-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 in turn generate appropriate answers to initiate resolution of inflammation. It appears that multiple pathways in the inflammatory microenvironment are used to adjust HIF-1alpha 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.

摘要

缺氧诱导因子(HIF)是一种转录激活因子,可协调对缺氧的适应性反应。在大多数临床相关的缺氧/缺血发作和人类癌症中,其活性都会升高。然而,对HIF-1α基因敲除小鼠的研究揭示了HIF-1在胚胎发育或糖酵解能量产生等生理过程中的重要作用。HIF-1活性不仅局限于氧供应减少的病理状况,而且通过调节氧的输送和消耗对于正常的氧稳态也是必需的,这一发现揭示了HIF-1在包括免疫系统在内的多个器官中迄今未被认识的多种功能。先天性免疫反应由巨噬细胞协调。这些细胞对环境输入信号作出反应,进而产生适当的应答以启动炎症的消退。炎症微环境中的多种途径似乎被用于调节HIF-1α水平以影响巨噬细胞生物学特性。本综述总结了哺乳动物免疫细胞尤其是巨噬细胞和中性粒细胞中HIF激活的机制,并概述了HIF如何调节炎症。

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