Mitochondrial criticality: A new concept at the turning point of life or death

被引:114
作者
Aon, MA [1 ]
Cortassa, S [1 ]
Akar, FG [1 ]
O'Rourke, B [1 ]
机构
[1] Johns Hopkins Univ, Div Cardiol, Inst Mol Cardiobiol, Baltimore, MD 21205 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2006年 / 1762卷 / 02期
关键词
mitochondrial oscillation; oxidative stress; inner membrane anion channel; ischemia-reperfusion injury; arrhythmias;
D O I
10.1016/j.bbadis.2005.06.008
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
A variety of stressors can cause the collapse of mitochondrial membrane potential (A P.), but the events leading up to this catastrophic cellular event are not well understood at the mechanistic level. Based on our recent studies of oscillations in mitochondrial energetics, we have coined the term "mitochondrial criticality" to describe the state in which the mitochondrial network of cardiomyocytes becomes very sensitive to small perturbations in reactive oxygen species (ROS), resulting in the scaling of local mitochondrial uncoupling and A IF. loss to the whole cell, and the myocardial syncytium. At the point of criticality, the dynamics of the mitochondrial network bifurcate to oscillatory behavior. These energetic changes are translated into effects on the electrical excitability of the cell, inducing dramatic changes in the morphology and the threshold for activating an action potential. Emerging evidence suggests that this mechanism, by creating spatial and temporal heterogeneity of excitability in the heart during ischemia and reperfusion, underlies the genesis of potentially lethal cardiac arrhythmias. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:232 / 240
页数:9
相关论文
共 60 条
[1]  
AKAR FG, IN PRESS J CLIN INVE
[2]   IDENTIFICATION OF ANION AND CATION PATHWAYS IN THE INNER MITOCHONDRIAL-MEMBRANE BY PATCH CLAMPING OF MOUSE-LIVER MITOPLASTS [J].
ANTONENKO, YN ;
KINNALLY, KW ;
TEDESCHI, H .
JOURNAL OF MEMBRANE BIOLOGY, 1991, 124 (02) :151-158
[3]  
Aon MA, 2005, BIOPHYS J, V88, p446A
[4]   Percolation and criticality in a mitochondrial network [J].
Aon, MA ;
Cortassa, S ;
O'Rourke, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (13) :4447-4452
[5]   The fractal architecture of cytoplasmic organization: Scaling, kinetics and emergence in metabolic networks [J].
Aon, MA ;
O'Rourke, B ;
Cortassa, S .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 256 (1-2) :169-184
[6]   Synchronized whole cell oscillations in mitochondrial metabolism triggered by a local release of reactive oxygen species in cardiac myocytes [J].
Aon, MA ;
Cortassa, S ;
Marbán, E ;
O'Rourke, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (45) :44735-44744
[7]   Gene expression and the thiol redox state [J].
Arrigo, AP .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (9-10) :936-944
[8]  
Bak P., 1996, NATURE WORKS SCI SEL
[9]  
BEAVIS AD, 1987, J BIOL CHEM, V262, P15085
[10]   The mitochondrial inner membrane anion channel is inhibited by DIDS [J].
Beavis, AD ;
DavatolHag, H .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1996, 28 (02) :207-214