The function of hypoxia-inducible factor 1 (HIF-1) is impaired in senescent mice

被引:103
|
作者
Frenkel-Denkberg, G
Gershon, D [1 ]
Levy, AP
机构
[1] Technion Israel Inst Technol, Dept Biol, IL-32000 Haifa, Israel
[2] Technion Israel Inst Technol, Fac Med, Haifa, Israel
基金
以色列科学基金会;
关键词
aging; stress; hypoxia; angiogenesis; collateral circulation;
D O I
10.1016/S0014-5793(99)01552-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Senescent organisms respond poorly to hypoxic stress. The transcription factor hypoxia-inducible factor 1 (HIF-1) plays a critical role in the coordinated genetic program that is induced in all tissues to adapt to hypoxic stress by binding to a specific DNA hypoxia-responsive recognition element (HRE). This study was designed to address whether aging is associated with an alteration in HIF-1 production and function. Young and old mice were exposed to hypoxia for various lengths of time. We found a severe impairment in the capacity of the old animals to form a HIF-1-HRE complex. This attenuation in the capacity to form HIF-1-HRE complexes in senescent tissues may explain the decreased ability of such tissues to respond to hypoxic stress, (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:341 / 344
页数:4
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