CDC2 ACTIVATION IS NOT REQUIRED FOR THYMOCYTE APOPTOSIS

被引:54
作者
NORBURY, C
MACFARLANE, M
FEARNHEAD, H
COHEN, GM
机构
[1] MRC,TOXICOL UNIT,LEICESTER LE1 9HN,ENGLAND
[2] UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,ICRF,MOLEC ONCOL LAB,OXFORD OX3 9DU,ENGLAND
关键词
D O I
10.1006/bbrc.1994.2086
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
Apoptosis is a mode of cell death characterized by chromatin condensation and disassembly of the nuclear lamina, processes that are also characteristic of mitosis. The apparent similarity between the two events, together with observations that apoptosis can occur following G2 arrest, has led to the suggestion that apoptosis could be a defective form of mitosis. Further support for this idea comes from the recent description of activation of the p34(cdc2) protein kinase (Cdc2), the universal M-phase promoter, during death induced by a lymphocyte granule protease. We have monitored the protein kinase activity of Cdc2 during apoptosis of primary rat thymocytes which die from a quiescent (G(0)) state. We demonstrate unequivocally that activation of Cdc2 is not involved in the induction of apoptosis in thymocytes, indicating that chromatin condensation and lamina disassembly occur in this system by processes different from those that operate in mitosis. (C) 1994 Academic Press, Inc.
引用
收藏
页码:1400 / 1406
页数:7
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