Modulation of endoplasmic reticulum calcium pump by Bcl-2

被引:168
作者
Kuo, TH [1 ]
Kim, HRC [1 ]
Zhu, LP [1 ]
Yu, YJ [1 ]
Lin, HM [1 ]
Tsang, W [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
关键词
Bcl-2; endoplasmic reticulum calcium pump; gene expression;
D O I
10.1038/sj.onc.1202110
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
Members of the bcl-2 gene family encode proteins that function either to promote or to inhibit apoptosis. Despite numerous efforts, the mechanism of action of Bcl-2, an anti-apoptotic protein, is still not clear. In particular, the relation between Bcl-2 and the endoplasmic reticulum (ER) calcium store is not well-understood. In the present work, we examined the effect of Bcl-2 on the ER store. We demonstrate that overexpression of Bcl-2 in breast epithelial cells modulates ER store by upregulating calcium pump (SERCA) expression,without affecting the release channel (IP3R). The steady state levels of SERCA2 mRNA and protein were both increased in Bcl-2 expression clones. The increase in SERCA2 protein leads to accelerated calcium uptake and enhanced Ca2+ loading. In addition, we also show the detection of intracellular interaction between Bcl-2 and SERCA molecules by co-immunoprecipitation. Since high lumenal Ca2+ concentration of ER is essential for normal cell functions, the results suggest that Bcl-2 preserves the ER Ca2+ store by upregulating SERCA gene expression as well as by a possible interaction with the pump.
引用
收藏
页码:1903 / 1910
页数:8
相关论文
共 36 条
[1]   Inhibition of Bax channel-forming activity by Bcl-2 [J].
Antonsson, B ;
Conti, F ;
Ciavatta, A ;
Montessuit, S ;
Lewis, S ;
Martinou, I ;
Bernasconi, L ;
Bernard, A ;
Mermod, JJ ;
Mazzei, G ;
Maundrell, K ;
Gambale, F ;
Sadoul, R ;
Martinou, JC .
SCIENCE, 1997, 277 (5324) :370-372
[2]  
BAFFY G, 1993, J BIOL CHEM, V268, P6511
[3]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[4]   Roles of cytoplasmic Ca2+ and intracellular Ca2+ stores in induction and suppression of apoptosis in S49 cells [J].
Bian, XP ;
Hughes, FM ;
Huang, Y ;
Cidlowski, JA ;
Putney, JW .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (04) :C1241-C1249
[5]   Cloning and expression of a novel Mammalian homolog of Drosophila transient receptor potential (Trp) involved in calcium entry secondary to activation of receptors coupled by the G(q) class of G protein [J].
Boulay, G ;
Zhu, X ;
Peyton, M ;
Jiang, MS ;
Hurst, R ;
Stefani, E ;
Birnbaumer, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (47) :29672-29680
[6]  
BROSTROM CO, 1990, ANNU REV PHYSIOL, V52, P577
[7]  
CALPHAM DE, 1995, CELL, V80, P259
[8]   INTRACELLULAR CALCIUM HOMEOSTASIS [J].
CARAFOLI, E .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :395-433
[9]   The exit from G(0) into the cell cycle requires and is controlled by sarco(endo)plasmic reticulum Ca2+ pump [J].
Cheng, GM ;
Liu, BF ;
Yu, YJ ;
Diglio, C ;
Kuo, TH .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 329 (01) :65-72
[10]  
Distelhorst CW, 1996, ONCOGENE, V12, P2051