DE-NOVO SYNTHESIS OF GLUTATHIONE IS REQUIRED FOR BOTH ENTRY INTO AND PROGRESSION THROUGH THE CELL-CYCLE

被引:154
|
作者
POOT, M
TEUBERT, H
RABINOVITCH, PS
KAVANAGH, TJ
机构
[1] UNIV WURZBURG,DEPT HUMAN GENET,D-97074 WURZBURG,GERMANY
[2] UNIV WASHINGTON,DEPT PATHOL,SEATTLE,WA 98195
[3] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98195
[4] UNIV WASHINGTON,DIV PULM & CRIT CARE MED,SEATTLE,WA 98195
关键词
D O I
10.1002/jcp.1041630316
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To study the putative role of de novo synthesis of glutathione (GSH) in the regulation of the cell cycle, we exposed NIH-3T3 cells to buthionine sulfoximine (BSO) and analysed cell cycle kinetics with continuous bromodeoxyuridine (BrdU) labeling and bivariate Hoechst 33258/ethidium bromide flow cytometry. Treating quiescent cells, which themselves had a low GSH content, with BSO did not affect subsequent entry into and progression through the cell cycle. Adding BSO during serum stimulation, however, provoked a dose-dependent inhibition of cell growth and a delayed increase in GSH level. The cell kinetic mechanism underlying BSO-induced growth inhibition is a diminished entry into the cell cycle and a permanent arrest in the S and G2 phase of the cell cycle. Our results are consistent with the hypothesis that GSH de novo synthesis is required for cell activation and proper S and G2 phase transit. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:555 / 560
页数:6
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