Release of cytochrome c from heart mitochondria is induced by high Ca2+ and peroxynitrite and is responsible for Ca2+-induced inhibition of substrate oxidation

被引:111
作者
Borutaite, V
Morkuniene, R
Brown, GC
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] Kaunas Med Univ, Inst Biomed Res, LT-3007 Kaunas, Lithuania
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1999年 / 1453卷 / 01期
基金
英国惠康基金;
关键词
heart ischaemia; cytochrome C; oxidative phosphorylation; calcium; apoptosis;
D O I
10.1016/S0925-4439(98)00082-9
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
Prolonged heart ischaemia causes an inhibition of oxidative phosphorylation and an increase of Ca2+ in mitochondria. We investigated whether elevated Ca2+ induces changes in the oxidative phosphorylation system relevant to ischaemic damage, and whether Ca2+ and other inducers of mitochondrial permeability transition cause the release of cytochrome c from isolated heart mitochondria. We found that 5 mu M free Ca2+ induced changes in oxidative phosphorylation system similar to ischaemic damage: increase in the proton leak and inhibition of the substrate oxidation system related to the release of cytochrome c from mitochondria. The phosphorylating system was not directly affected by high Ca2+ and ischaemia. The release of cytochrome c from mitochondria was caused by Ca2+ and 0.175-0.9 mM peroxynitrite but not by NO, and was prevented by cyclosporin A. Adenylate kinase and creatine kinase were also released after incubation of mitochondria with Ca2+, however, the activity of citrate synthase in the incubation medium with high and low Ca2+ did not change. The data suggest that release of cytochrome c and other proteins of intermembrane space may be due to the opening of the mitochondrial permeability transition pore, and may be partially responsible for inhibition of mitochondrial respiration induced by ischaemia, high calcium, and oxidants. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
相关论文
共 33 条
  • [1] ALLEN SP, 1993, J MOL CELL CARDIOL, V25, P948
  • [2] THE REVERSIBLE CA-2+-INDUCED PERMEABILIZATION OF RAT-LIVER MITOCHONDRIA
    ALNASSER, I
    CROMPTON, M
    [J]. BIOCHEMICAL JOURNAL, 1986, 239 (01) : 19 - 29
  • [3] APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE
    BECKMAN, JS
    BECKMAN, TW
    CHEN, J
    MARSHALL, PA
    FREEMAN, BA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) : 1620 - 1624
  • [4] BERNARDI P, 1992, J BIOL CHEM, V267, P2934
  • [5] Myocyte apoptosis during acute myocardial infarction in the mouse localizes to hypoxic regions but occurs independently of p53
    Bialik, S
    Geenen, DL
    Sasson, IE
    Cheng, R
    Horner, JW
    Evans, SM
    Lord, EM
    Koch, CJ
    Kitsis, RN
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (06) : 1363 - 1372
  • [6] Kinetic analysis of changes in activity of heart mitochondrial oxidative phosphorylation system induced by ischemia
    Borutaite, V
    Morkuniene, R
    Budriunaite, A
    Krasauskaite, D
    Ryselis, S
    Toleikis, A
    Brown, GC
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (10) : 2195 - 2201
  • [7] BROEKEMEIER KM, 1985, J BIOL CHEM, V260, P105
  • [8] BROWN GC, 1995, BIOENERGETICS PRACTI, P111
  • [9] ENHANCEMENT OF HYDROGEN-PEROXIDE FORMATION BY PROTOPHORES AND IONOPHORES IN ANTIMYCIN-SUPPLEMENTED MITOCHONDRIA
    CADENAS, E
    BOVERIS, A
    [J]. BIOCHEMICAL JOURNAL, 1980, 188 (01) : 31 - 37
  • [10] PERMEABILIZATION OF THE INNER MITOCHONDRIAL-MEMBRANE BY CA2+ IONS IS STIMULATED BY T-BUTYL HYDROPEROXIDE AND MEDIATED BY REACTIVE OXYGEN SPECIES GENERATED BY MITOCHONDRIA
    CASTILHO, RF
    KOWALTOWSKI, AJ
    MEINICKE, AR
    BECHARA, EJH
    VERCESI, AE
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (03) : 479 - 486