SV40 T/t-antigens sensitize mammary gland epithelial cells to oxidative stress and apoptosis

被引:6
作者
Kohlhoff, S [1 ]
Ziechmann, C [1 ]
Gottlob, K [1 ]
Graessmann, M [1 ]
机构
[1] Free Univ Berlin, Inst Molekularbiol & Biochem, D-14195 Berlin, Germany
关键词
SV40; T/t-antigens; apoptosis; oxidative stress; H2O2; catalase; free radicals;
D O I
10.1016/S0891-5849(00)00340-3
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
As shown recently, the SV40 T/t-antigens (T/t-ag) exert a strong apoptotic activity in mouse mammary gland epithelial cells (ME-cells) leading to premature gland involution at late pregnancy. This high spontaneous cell death rate (20%) is also maintained in T/t-ag positive ME-tissue culture cell lines (e.g., 8/61-A), but not in those ME-cells that have switched off the SV40 T/t-transgene expression. In this study, we demonstrate for the first time that the T/t-ag sensitize ME-Sells to oxidative stress leading to apoptosis. Treatment of the 8/61-A ME-cells with catalase, a scavenger of H2O2, completely blocked spontaneous cell death, which was linked to downregulation of caspase-3 activity. Furthermore, exposure of the cells to low concentrations of H2O2 highly increased the apoptosis rate. These findings suggest that the T/t-ag positive ME-cells contain either elevated levels of reactive oxygen species or reduced antioxidant activities. During spontaneous and H2O2-induced apoptosis, the activity of caspase-3 is significantly increased. In addition, the 8/61-A cells accumulated p21 and Bar proteins while the level of the anti-apoptotic protein Bcl-2 decreased implying a posttranscriptional regulation of apoptosis. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:497 / 506
页数:10
相关论文
共 49 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   THE BALANCE BETWEEN CU,ZN-SUPEROXIDE DISMUTASE AND CATALASE AFFECTS THE SENSITIVITY OF MOUSE EPIDERMAL-CELLS TO OXIDATIVE STRESS [J].
AMSTAD, P ;
PESKIN, A ;
SHAH, G ;
MIRAULT, ME ;
MORET, R ;
ZBINDEN, I ;
CERUTTI, P .
BIOCHEMISTRY, 1991, 30 (38) :9305-9313
[3]   SUPEROXIDE AND HYDROGEN-PEROXIDE IN RELATION TO MAMMALIAN-CELL PROLIFERATION [J].
BURDON, RH .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (04) :775-794
[4]   OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS [J].
BUTTKE, TM ;
SANDSTROM, PA .
IMMUNOLOGY TODAY, 1994, 15 (01) :7-10
[5]   PROOXIDANT STATES AND TUMOR PROMOTION [J].
CERUTTI, PA .
SCIENCE, 1985, 227 (4685) :375-381
[6]  
Clutton S, 1997, BRIT MED BULL, V53, P662
[7]   Identification of a novel antiapoptotic functional domain in simian virus 40 large T antigen [J].
Conzen, SD ;
Snay, CA ;
Cole, CN .
JOURNAL OF VIROLOGY, 1997, 71 (06) :4536-4543
[8]   Activation of caspase 3 in HL-60 cells exposed to hydrogen peroxide [J].
DiPietrantonio, AM ;
Hsieh, TC ;
Wu, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 255 (02) :477-482
[9]   WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION [J].
ELDEIRY, WS ;
TOKINO, T ;
VELCULESCU, VE ;
LEVY, DB ;
PARSONS, R ;
TRENT, JM ;
LIN, D ;
MERCER, WE ;
KINZLER, KW ;
VOGELSTEIN, B .
CELL, 1993, 75 (04) :817-825
[10]   Redox-mediated regulation of p21(waf1/cip1) expression involves a post-transcriptional mechanism and activation of the mitogen-activated protein kinase pathway [J].
Esposito, F ;
Cuccovillo, F ;
Vanoni, M ;
Cimino, F ;
Anderson, CW ;
Appella, E ;
Russo, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 245 (03) :730-737