Redox Aspects of Bcl-2 Function

被引:105
作者
Voehringer, David W. [1 ]
Meyn, Raymond E. [2 ]
机构
[1] Stanford Univ, Sch Med, Dept Genet, Beckman Ctr, Stanford, CA 94305 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
D O I
10.1089/15230860050192314
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
The oncogene Bcl-2 has attracted recent research attention as recognition of the importance of Bcl-2 control over apoptosis commitment in disease development and clinical response to therapy has been targeted for pharmacological intervention. Much of the basic science research regarding Bcl-2 has focused on the role that Bcl-2 plays in directly regulating mitochondrial function. This has come about because of Bcl-2's localization to mitochondrial membranes and its reported interaction with the mitochondrial megachannel. During the time that the mitochondrial function of Bcl-2 was being investigated, a smaller, yet potentially as important, role for Bcl-2 was being pursued by investigators who were following up the initial study of Bcl-2 knockout mice. These mice expressed a phenotype consistent with that of mice exposed to chronic oxidative stress. This research into the redox aspects of Bcl-2 function has led to a hypothesis that Bcl-2-expressing cells have enhanced antioxidant capacities that suppress oxidative stress signals generated during the initiation phase of many apoptotic pathways. This review will further develop the idea of Bcl-2's role in regulating cellular redox pathways associated with apoptosis, as well as integrate recently reported evidence that ties the antioxidant effects of Bcl-2 to mitochondrial function, thereby unifying both mitochondrial and redox aspects of Bcl-2 function. Antiox. Redox Signal. 2, 537-550.
引用
收藏
页码:537 / 550
页数:14
相关论文
共 75 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]  
Baker A, 1997, CANCER RES, V57, P5162
[3]   Apoptotic process in the monkey small intestinal epithelium: I. Association with glutathione level and its efflux [J].
Benard, O ;
Madesh, M ;
Anup, R ;
Balasubramanian, KA .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (3-4) :245-252
[4]   Uncoupling protein-3: A new member of the mitochondrial carrier family with tissue-specific expression [J].
Boss, O ;
Samec, S ;
PaoloniGiacobino, A ;
Rossier, C ;
Dulloo, A ;
Seydoux, J ;
Muzzin, P ;
Giacobino, JP .
FEBS LETTERS, 1997, 408 (01) :39-42
[5]   REDOX REGULATION OF PROGRAMMED CELL-DEATH IN LYMPHOCYTES - INVITED COMMENTARY [J].
BUTTKE, TM ;
SANDSTROM, PA .
FREE RADICAL RESEARCH, 1995, 22 (05) :389-397
[6]   Mitochondrial control of apoptosis:: the role of cytochrome c [J].
Cai, JY ;
Yang, J ;
Jones, DP .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1366 (1-2) :139-149
[7]   Communication -: Superoxide in apoptosis -: Mitochondrial generation triggered by cytochrome c loss [J].
Cai, JY ;
Jones, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11401-11404
[8]   HUMAN UNCOUPLING PROTEIN GENE - STRUCTURE, COMPARISON WITH RAT GENE, AND ASSIGNMENT TO THE LONG ARM OF CHROMOSOME-4 [J].
CASSARD, AM ;
BOUILLAUD, F ;
MATTEI, MG ;
HENTZ, E ;
RAIMBAULT, S ;
THOMAS, M ;
RICQUIER, D .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1990, 43 (03) :255-264
[9]   Mitochondria and cells produce reactive oxygen species in virtual anaerobiosis: relevance to ceramide-induced apoptosis [J].
Degli Esposti, M ;
McLennan, H .
FEBS LETTERS, 1998, 430 (03) :338-342
[10]   Studies on oxidative damage induced by cyanobacteria extract in primary cultured rat hepatocytes [J].
Ding, WX ;
Shen, HM ;
Zhu, HG ;
Ong, CN .
ENVIRONMENTAL RESEARCH, 1998, 78 (01) :12-18