Bad overexpression sensitizes NIH/3T3 cells to undergo apoptosis which involves caspase activation and ERK inactivation

被引:23
作者
Jan, MS [1 ]
Liu, HS [1 ]
Lin, YS [1 ]
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Microbiol & Immunol, Tainan 70101, Taiwan
关键词
D O I
10.1006/bbrc.1999.1475
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 effect of Bad overexpression on apoptosis was demonstrated by a mouse Bad transgene stably expressed in NIH/3T3 cells. The cells overexpressing Bad treated with either serum starvation or ceramide showed apoptotic characteristics evident at 18 and 8 h, respectively. Whether serum deprivation and ceramide utilize a common death pathway requires further investigation. The time for the first apoptosis detection was shortened to 2 h and was prominent at 4 h, while above that time cells were maintained under serum-depleted conditions in the presence of ceramide (40 mu M). Further investigation revealed that the activity of caspase-3 (CPP32) was elevated after ceramide treatment in Bad-transfected cells compared to that of the cells without Bad transfection, indicating the involvement of caspase cascade. Furthermore, the Bad-transfected cells showed reduced phosphorylation of extracellular signal-regulated kinase (EBB). Taken together, we hypothesize that Bad-overexpressing NIH/3T3 cells in the presence of ceramide undergo apoptosis by activating caspase cascade. Simultaneously, the cell survival pathway was blocked possibly by inactivation of the MAPK pathway such as the down-regulation of ERK. (C) 1999 Academic Press.
引用
收藏
页码:724 / 729
页数:6
相关论文
共 31 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   BAD enables ceramide to signal apoptosis via Ras and Raf-1 [J].
Basu, S ;
Bayoumy, S ;
Zhang, Y ;
Lozano, J ;
Kolesnick, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30419-30426
[3]   Stress signals for apoptosis: ceramide and c-Jun kinase [J].
Basu, S ;
Kolesnick, R .
ONCOGENE, 1998, 17 (25) :3277-3285
[4]   The Kit receptor promotes cell survival via activation of PI 3-kinase and subsequent Akt-mediated phosphorylation of Bad on Ser136 [J].
Blume-Jensen, P ;
Janknecht, R ;
Hunter, T .
CURRENT BIOLOGY, 1998, 8 (13) :779-782
[5]   CERAMIDE SYNTHASE MEDIATES DAUNORUBICIN-INDUCED APOPTOSIS - AN ALTERNATIVE MECHANISM FOR GENERATING DEATH SIGNALS [J].
BOSE, R ;
VERHEIJ, M ;
HAIMOVITZFRIEDMAN, A ;
SCOTTO, K ;
FUKS, Z ;
KOLESNICK, R .
CELL, 1995, 82 (03) :405-414
[6]  
Boussiotis VA, 1997, J IMMUNOL, V159, P3156
[7]   BCL-2 FAMILY: Regulators of cell death [J].
Chao, DT ;
Korsmeyer, SJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :395-419
[8]   Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[9]  
delPeso L, 1997, SCIENCE, V278, P687
[10]   Ceramide, AIDS and long-term survivors [J].
DeSimone, C ;
Cifone, MG ;
Roncaioli, P ;
Moretti, S ;
Famularo, G ;
Alesse, E ;
Boschini, A ;
Testi, R .
IMMUNOLOGY TODAY, 1996, 17 (01) :48-48