p53-dependent apoptosis induced by proteasome inhibition in mammary epithelial cells

被引:70
|
作者
MacLaren, AP
Chapman, RS
Wyllie, AH
Watson, CJ
机构
[1] Western Gen Hosp, Mol Med Ctr, Sir Alastair Currie CRC Labs, Edinburgh EH2 4XU, Midlothian, Scotland
[2] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
关键词
KIM-2 mammary epithelial cells; p53; apoptosis; 26S proteasome;
D O I
10.1038/sj.cdd.4400801
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
We have examined the effects of inhibition of the 26S proteasome in a murine mammary cell line, KIM-2 cells using the peptide aldehyde inhibitor MG132, These studies have demonstrated a clear requirement for proteasome function in cell viability. Induction of apoptosis was observed following MG132 treatment in KIM-2 cells and this death was shown to be dependent on the cell actively traversing the cell cycle. KIM-2 cells were generated using a temperature sensitive T-antigen (Tag) and studies at the permissive temperature (33 C) have shown that a Tag binding protein was essential for this apoptotic response, Studies in two additional cell lines, HC11, which is a mammary epithelial cell line carrying mutant p53 alleles and p53 null ES cells suggest that p53 is actively required for the apoptosis induced as a consequence of proteasome inhibition, These results suggest a pivotal role for the 26S proteasome degradation pathway in progression through the cell cycle in proliferating cells.
引用
收藏
页码:210 / 218
页数:9
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