Hypoxia inducible factor (HIF) function in innate immunity and infection

被引:226
作者
Zinkernagel, Annelies S.
Johnson, Randall S.
Nizet, Victor
机构
[1] Univ Calif San Diego, Sch Med, Div Pediat Pharmacol & Drug Discovery, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2007年 / 85卷 / 12期
关键词
HIF-1; hypoxia; innate immunity; phagocyte; neutrophil; macrophage;
D O I
10.1007/s00109-007-0282-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The hypoxia-inducible transcription factor (HIF-1 alpha) is a major regulator of energy homeostasis and cellular adaptation to low oxygen stress. Recently, HIF-1 alpha has been discovered to function as a global regulator of macrophage and neutrophil inflammatory and innate immune functions, as befits these specialized phagocytic cells who must operate effectively in the hypoxic microenvironments of infected tissues. This review summarizes current knowledge of the role of HIF-1 alpha in mammalian innate immunity, emphasizing insight gained from conditional gene targeting of the transcription factor in the myeloid cell lineage. Dynamic changes in HIF-1 alpha expression in the course of bacterial, viral, or parasitic infections are outlined and inferences drawn regarding the consequences for pathogen and host. A better understanding of HIF-1 alpha function may provide novel and rational approaches for boosting innate immune function in the therapy of certain complicated infectious disease conditions.
引用
收藏
页码:1339 / 1346
页数:8
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