Mitochondrial complex III is required for hypoxia-induced ROS production and cellular oxygen sensing

被引:1235
|
作者
Guzy, RD
Hoyos, B
Robin, E
Chen, H
Liu, LP
Mansfield, KD
Simon, MC
Hammerling, U
Schumacker, PT
机构
[1] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[2] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10021 USA
[3] Univ Penn, Howard Hughes Med Inst, Philadelphia, PA 19104 USA
[4] Univ Penn, Abramson Family Canc Inst, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/j.cmet.2005.05.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multicellular organisms initiate adaptive responses when oxygen (02) availability decreases, but the underlying mechanism Of 02 sensing remains elusive. We find that functionality of complex III of the mitochondrial electron transport chain (ETC) is required for the hypoxic stabilization of HIF-1 alpha and HIF-2 alpha. and that an increase in reactive oxygen species (ROS) links this complex to HIF-alpha. stabilization. Using RNAi to suppress expression of the Rieske iron-sulfur protein of complex III, hypoxia-induced HIF-1 alpha stabilization is attenuated, and ROS production, measured using a novel ROS-sensitive FRET probe, is decreased. These results demonstrate that mitochondria function as O-2 sensors and signal hypoxic HIF-1 alpha and HIF-2 alpha stabilization by releasing ROS to the cytosol.
引用
收藏
页码:401 / 408
页数:8
相关论文
共 50 条
  • [1] Mitochondrial complex III is required for hypoxia-induced ROS production and gene transcription in yeast
    Guzy, Robert D.
    Mack, Matthew M.
    Schumacker, Paul T.
    ANTIOXIDANTS & REDOX SIGNALING, 2007, 9 (09) : 1317 - 1328
  • [2] Terpestacin Inhibits Tumor Angiogenesis by Targeting UQCRB of Mitochondrial Complex III and Suppressing Hypoxia-induced Reactive Oxygen Species Production and Cellular Oxygen Sensing
    Jung, Hye Jin
    Shim, Joong Sup
    Lee, Jiyong
    Song, Young Mi
    Park, Ki Chung
    Choi, Seung Hoon
    Kim, Nam Doo
    Yoon, Jeong Hyeok
    Mungai, Paul T.
    Schumacker, Paul T.
    Kwon, Ho Jeong
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (15) : 11584 - 11595
  • [3] Oxygen sensing and hypoxia-induced responses
    Coleman, Mathew L.
    Ratcliffe, Peter J.
    OXYGEN SENSING AND HYPOXIA-INDUCED RESPONSES, 2007, 43 : 1 - 15
  • [4] Mitochondrial complex II is essential for hypoxia-induced ROS generation and vasoconstriction in the pulmonary vasculature
    Paddenberg, R
    Goldenberg, A
    Faulhammer, P
    Braun-Dullaeus, RC
    Kummer, W
    CHEMORECEPTION: FROM CELLULAR SIGNALLING TO FUNCTIONAL PLASTICITY, 2003, 536 : 163 - 169
  • [5] Mitochondrial reactive oxygen species are required for hypoxia-induced degradation of keratin intermediate filaments
    Na, Ni
    Chandel, Navdeep S.
    Litvan, Juan
    Ridge, Karen M.
    FASEB JOURNAL, 2010, 24 (03): : 799 - 809
  • [6] Mitochondrial reactive oxygen species are required for hypoxia-induced degradation of keratin intermediate filaments
    Ridge, Karen M.
    Litvan, Juan
    Ni, Na
    FASEB JOURNAL, 2009, 23
  • [7] Hypoxia-Induced Mitochondrial ROS and Function in Pulmonary Arterial Endothelial Cells
    Wang, Harrison
    Song, Teng-Yao
    Reyes-Garcia, Jorge
    Wang, Yong-Xiao
    CELLS, 2024, 13 (21)
  • [8] Mitochondrial complex I ROS production and redox signaling in hypoxia
    Okoye, Chidozie N.
    Koren, Shon A.
    Wojtovich, Andrew P.
    REDOX BIOLOGY, 2023, 67
  • [9] Mitochondrial reactive oxygen species trigger hypoxia-induced transcription
    Chandel, NS
    Maltepe, E
    Goldwasser, E
    Mathieu, CE
    Simon, MC
    Schumacker, PT
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) : 11715 - 11720
  • [10] Mitochondria as source of intermittent hypoxia-induced reactive oxygen species (ROS) generation
    McCormick, AA
    Holcroft, JJ
    Kim, DK
    Prabhakar, NN
    Kumar, GK
    FASEB JOURNAL, 2003, 17 (05): : A954 - A954