Compound C inhibits hypoxic activation of HIF-1 independent of AMPK

被引:93
作者
Emerling, Brooke M. [1 ,4 ]
Viollet, Benoit [2 ,3 ]
Tormos, Kathryn V. [4 ]
Chandel, Navdeep S. [4 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Signal Transduct, Boston, MA 02115 USA
[2] Univ Paris 05, Inst Cochin, CNRS, UMR 8104, Paris, France
[3] INSERM, U567, Paris, France
[4] Northwestern Univ, Dept Med, Chicago, IL 60611 USA
关键词
hypoxia inducible factor 1; AMP-activated kinase; compound C; hypoxia; mitochondria; reactive oxygen species;
D O I
10.1016/j.febslet.2007.11.038
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
The key transcription factor that regulates the cellular responses to hypoxia is hypoxia inducible factor-1 (HIF-1). The signaling mechanisms that regulate the hypoxic activation of HIF-1 are not fully understood. Our objective here was to test whether AMP-activated kinase (AMPK) was an upstream regulator of HIF-1. Our results show that AMPK is not required for the hypoxic activation of HIF-1. Interestingly, the AMPK inhibitor, Compound C, inhibits the hypoxic activation of HIF-1 independent of AMPK. Furthermore, we demonstrate that Compound C functions as a repressor of HIF-1 by inhibiting respiration and suppressing mitochondrial generated ROS. (C) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:5727 / 5731
页数:5
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