Overexpression of cdk4/cyclin D1 induces apoptosis in PC12 cells in the presence of trophic support

被引:17
作者
Katayama, K
Dobashi, Y
Kitagawa, M
Kamekura, S
Kawai, M
Kadoya, Y
Kameya, T
机构
[1] Kitasato Univ, Sch Med, Dept Pathol, Kanagawa 2288555, Japan
[2] Hamamatsu Univ Sch Med, Dept Biochem 1, Shizuoka, Japan
[3] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama, Japan
[4] Kitasato Univ, Sch Med, Dept Anaesthesia, Kanagawa 2288555, Japan
关键词
cdk4; cyclin D1; PC12; cell; apoptosis; cdk inhibitor; dominant negative cdk4;
D O I
10.1016/S0014-5793(01)03200-8
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 induction of apoptosis by cell cycle regulator molecules under conditions optimal for exponential growth was examined in rat pheochromocytoma PC12 cells by overexpression of cyclins and cyclin-dependent kinases (cdks). By flow cytometry and by immunofluorescence, only cells overexpressing cdk-4 or cyclin D1 underwent apoptosis, which was not associated with G1-arrest. Cdk4 kinase activity was significantly higher in cdk4-, or cyclin D1-expressing cells. Furthermore, induction of apoptosis by cdk-4 was abrogated by co-transfection of p16(INK4), or dominant negative cdk4. These results suggest that upregulation of cdk4 kinase activity is a primary and critical mediator of apoptosis in PC12 cells under physiological conditions. (C) 2001 Federation of European Biochemical Societies., Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:382 / 388
页数:7
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