Mitochondrial permeability transition and swelling can occur reversibly without inducing cell death in intact human cells

被引:167
作者
Minamikawa, T
Williams, DA
Bowser, DN
Nagley, P [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3168, Australia
[2] Univ Melbourne, Dept Physiol, Confocal & Fluorescence Imaging Grp, Parkville, Vic 3052, Australia
基金
英国医学研究理事会;
关键词
mitochondrial permeability transition; mitochondrial swelling; mitochondrial membrane potential; fluorescence; confocal microscopy;
D O I
10.1006/excr.1998.4290
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Severe disruption of mitochondrial function is generally considered to provide a powerful trigger for apoptosis in mammalian cells. We report here that intact cells may undergo the mitochondrial permeability transition and mitochondria swell in a fully reversible manner, without inducing cell death. Cultured human osteosarcoma cells (143B TK-) stained with JC-1, MitoTracker dyes, or calcein plus Co2+ were imaged by confocal microscopy to visualize changes of mitochondrial membrane potential (Delta Psi(m)), morphology, and permeability transition, respectively, during treatment with a protonophore, carbonyl cyanide m-chlorophenylhydrazone (CCCP), Cells rapidly exhibited mitochondrial permeability transition and swelling after addition of CCCP, but the swelling subsided within hours, leaving mitochondria that appeared in punctate form, not filamentous as before CCCP treatment. Cyclosporin A impeded the permeability transition and swelling, although complete inhibition was not observed. Cells survived the dissipation of Delta Psi(m) by CCCP for up to 6 h without developing any obvious cell damage or signs of apoptosis. With the restoration of Delta Psi(m) after removal of CCCP (following 6 h of CCCP treatment), permeability transition pores were closed. These results suggest that none of the following events represent a point of no return in the process of apoptotic cell death: loss of Delta Psi(m) mitochondrial permeability transition, or mitochondrial swelling, (C) 1999 Academic Press.
引用
收藏
页码:26 / 37
页数:12
相关论文
共 36 条
[1]
GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[2]
[Anonymous], 1963, ANAL CHEM, DOI DOI 10.1021/AC60201A035
[3]
BERNARDI P, 1993, J BIOL CHEM, V268, P1005
[4]
Mitochondrial cytochrome c release in apoptosis occurs upstream of DEVD-specific caspase activation and independently of mitochondrial transmembrane depolarization [J].
Bossy-Wetzel, E ;
Newmeyer, DD ;
Green, DR .
EMBO JOURNAL, 1998, 17 (01) :37-49
[5]
Role of mitochondria in calcium regulation of spontaneously contracting cardiac muscle cells [J].
Bowser, DN ;
Minamikawa, T ;
Nagley, P ;
Williams, DA .
BIOPHYSICAL JOURNAL, 1998, 75 (04) :2004-2014
[6]
Distinct alterations in mitochondrial mass and function characterize different models of apoptosis [J].
Camilleri-Broët, S ;
Vanderwerff, H ;
Caldwell, E ;
Hockenbery, D .
EXPERIMENTAL CELL RESEARCH, 1998, 239 (02) :277-292
[7]
Cyclosporin A increases resting mitochondrial membrane potential in SY5Y cells and reverses the depressed mitochondrial membrane potential of Alzheimer's disease cybrids [J].
Cassarino, DS ;
Swerdlow, RH ;
Parks, JK ;
Parker, WD ;
Bennett, JP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (01) :168-173
[8]
MECHANISMS BY WHICH MITOCHONDRIA TRANSPORT CALCIUM [J].
GUNTER, TE ;
PFEIFFER, DR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (05) :C755-C786
[9]
CALCIUM ION-DEPENDENT SIGNALING AND MITOCHONDRIAL DYSFUNCTION - MITOCHONDRIAL CALCIUM-UPTAKE DURING HORMONAL-STIMULATION IN INTACT LIVER-CELLS AND ITS IMPLICATION FOR THE MITOCHONDRIAL PERMEABILITY TRANSITION [J].
HOEK, JB ;
FARBER, JL ;
THOMAS, AP ;
WANG, XL .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01) :93-102
[10]
Imaging the permeability pore transition in single mitochondria [J].
Hüser, J ;
Rechenmacher, CE ;
Blatter, LA .
BIOPHYSICAL JOURNAL, 1998, 74 (04) :2129-2137