Evaluation of fluorescent dyes for the detection of mitochondrial membrane potential changes in cultured cardiomyocytes

被引:213
作者
Mathur, A
Hong, Y
Kemp, BK
Barrientos, AA
Erusalimsky, JD
机构
[1] UCL, Dept Med, Ctr Vasc Biol & Med, Cell Biol Grp,Rayne Inst, London WC1E 6JJ, England
[2] UCL, Wolfson Inst Biomed Res, London WC1E 6AU, England
[3] Univ Complutense Madrid, Fac Farm, Ctr Citometria Flujo & Microscopia Confocal, E-28040 Madrid, Spain
基金
英国医学研究理事会;
关键词
apoptosis; cardiomyopathy; membrane potential; mitochondria; myocytes;
D O I
10.1016/S0008-6363(00)00002-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Maintenance of the mitochondrial membrane potential (Delta psi m) is fundamental for the normal performance and survival of cells such as cardiomyocytes, that have a high energy requirement. Measurement of Delta psi m is therefore essential in order to develop an understanding of the molecular mechanisms controlling cardiomyocyte function. Here We have evaluated various potentiometric dyes for their ability to detect alterations of Delta psi m. using flow cytometry and confocal microscopy. Methods: primary cultures of cardiomyocytes from neonate rats were treated with mitochondrial uncouplers before or after loading with Rho123. DiOC(6)(3), CMXRos or JC-1, and then analysed by flow cytometry. Apoptotic cells were identified by light scatter and Annexin V staining. Results: The four potentiometric dyes tested were able to discriminate between viable and apoptotic cells. However, only JC-1 was able to detect the collapse of Delta psi m induced by uncouplers of mitochondrial respiration. Confocal microscopic analysis confirmed that JC-1 stained mitochondria in a potential-dependent manner. In contrast. CMXRos stained cardiomyocytes irrespective of alterations in Delta psi m. Conclusions: We conclude that JC-1 is the optimal dye to use when measuring Delta psi m in cardiomyocytes. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:126 / 138
页数:13
相关论文
共 29 条
[1]   FLOW CYTOMETRIC ANALYSIS OF ISOLATED ADULT CARDIOMYOCYTES - VINCULIN AND TUBULIN FLUORESCENCE DURING METABOLIC INHIBITION AND ISCHEMIA [J].
ARMSTRONG, SC ;
GANOTE, CE .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1992, 24 (02) :149-162
[2]   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
[3]   Hibernation during hypoxia in cardiomyocytes -: Role of mitochondria as the O2 sensor [J].
Budinger, GRS ;
Duranteau, J ;
Chandel, NS ;
Schumacker, PT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (06) :3320-3326
[4]   A NEW METHOD FOR THE CYTOFLUOROMETRIC ANALYSIS OF MITOCHONDRIAL-MEMBRANE POTENTIAL USING THE J-AGGREGATE FORMING LIPOPHILIC CATION 5,5',6,6'-TETRACHLORO-1,1',3,3'-TETRAETHYLBENZIMIDAZOLCARBOCYANINE IODIDE (JC-1) [J].
COSSARIZZA, A ;
BACCARANICONTRI, M ;
KALASHNIKOVA, G ;
FRANCESCHI, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (01) :40-45
[5]   FEATURES OF APOPTOTIC CELLS MEASURED BY FLOW-CYTOMETRY [J].
DARZYNKIEWICZ, Z ;
BRUNO, S ;
DELBINO, G ;
GORCZYCA, W ;
HOTZ, MA ;
LASSOTA, P ;
TRAGANOS, F .
CYTOMETRY, 1992, 13 (08) :795-808
[6]  
DILISA F, 1995, J PHYSIOL-LONDON, V486, P1
[7]   ON THE INVOLVEMENT OF A CYCLOSPORINE-A SENSITIVE MITOCHONDRIAL PORE IN MYOCARDIAL REPERFUSION INJURY [J].
DUCHEN, MR ;
MCGUINNESS, O ;
BROWN, LA ;
CROMPTON, M .
CARDIOVASCULAR RESEARCH, 1993, 27 (10) :1790-1794
[8]   SIMULTANEOUS IMAGING OF CELL AND MITOCHONDRIAL-MEMBRANE POTENTIALS [J].
FARKAS, DL ;
WEI, MD ;
FEBBRORIELLO, P ;
CARSON, JH ;
LOEW, LM .
BIOPHYSICAL JOURNAL, 1989, 56 (06) :1053-1069
[9]   Sequence of metabolic changes during X-ray-induced apoptosis [J].
Ferlini, C ;
De Angelis, C ;
Biselli, R ;
Distefano, M ;
Scambia, G ;
Fattorossi, A .
EXPERIMENTAL CELL RESEARCH, 1999, 247 (01) :160-167
[10]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312