Cytochrome c is released in a single step during apoptosis

被引:178
作者
Goldstein, JC
Muñoz-Pinedo, C
Ricci, JE
Adams, SR
Kelekar, A
Schuler, M
Tsien, RY
Green, DR
机构
[1] La Jolla Inst Allergy & Immunol, San Diego, CA 92121 USA
[2] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[3] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[4] Johannes Gutenberg Univ Mainz, Dept Med 3, D-55101 Mainz, Germany
[5] Univ Calif San Diego, HHMI, Dept Chem & Biochem, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
关键词
apoptosis; cytochrome c; mitochondria; mitochondrial membrane potential; video microscopy;
D O I
10.1038/sj.cdd.4401596
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
Release of cytochrome c from mitochondria is a central event in apoptotic signaling. In this study, we utilized a cytochrome c fusion that binds fluorescent biarsenical ligands (cytochrome c-4CYS (cyt. c-4CYS)) as well as cytochrome c-green fluorescent protein ( cyt. c-GFP) to measure its release from mitochondria in different cell types during apoptosis. In single cells, the kinetics of cyt. c-4CYS release was indistinguishable from that of cyt. c-GFP in apoptotic cells expressing both molecules. Lowering the temperature by 7 degrees C did not affect this corelease, but further separated cytochrome c release from the subsequent decrease in mitochondrial membrane potential (Delta Psi(m)). Cyt. c-GFP rescued respiration in cells lacking endogenous cytochrome c, and the duration of cytochrome c release was approximately 5 min in a variety of cell types induced to die by various forms of cellular stress. In addition, we could observe no evidence of caspase-dependent amplification of cytochrome c release or changes in Delta Psi(m) preceding the release of cyt. c-GFP. We conclude that there is a general mechanism responsible for cytochrome c release that proceeds in a single step that is independent of changes in Delta Psi(m).
引用
收藏
页码:453 / 462
页数:10
相关论文
共 47 条
[41]   Bcl-2 proteins: regulators of apoptosis or of mitochondrial homeostasis? [J].
Vander Heiden, MG ;
Thompson, CB .
NATURE CELL BIOLOGY, 1999, 1 (08) :E209-E216
[42]  
Vander Heiden MG, 1999, MOL CELL, V3, P159
[43]   Bcl-x(L) regulates the membrane potential and volume homeostasis of mitochondria [J].
VanderHeiden, MG ;
Chandel, NS ;
Williamson, EK ;
Schumacker, PT ;
Thompson, CB .
CELL, 1997, 91 (05) :627-637
[44]   Preservation of mitochondrial structure and function after Bid- or Bax-mediated cytochrome c release [J].
von Ahsen, O ;
Renken, C ;
Perkins, G ;
Kluck, RM ;
Bossy-Wetzel, E ;
Newmeyer, DD .
JOURNAL OF CELL BIOLOGY, 2000, 150 (05) :1027-1036
[45]   And all of a sudden it's over: mitochondrial outer-membrane permeabilization in apoptosis [J].
Waterhouse, NJ ;
Ricci, JE ;
Green, DR .
BIOCHIMIE, 2002, 84 (2-3) :113-121
[46]   Cytochrome c maintains mitochondrial transmembrane potential and ATP generation after outer mitochondrial membrane permeabilization during the apoptotic process [J].
Waterhouse, NJ ;
Goldstein, JC ;
von Ahsen, O ;
Schuler, M ;
Newmeyer, DD ;
Green, DR .
JOURNAL OF CELL BIOLOGY, 2001, 153 (02) :319-328
[47]   Induction of the Mitochondrial Permeability Transition causes release of the apoptogenic factor cytochrome c [J].
Yang, JC ;
Cortopassi, GA .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (04) :624-631