Haupt Y, Barak Y, Oren M
Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
EMBO J. 1996 Apr 1;15(7):1596-606.
The effect of excess mdm2 on p53-mediated apoptosis was investigated in two human-derived cell lines, H1299 and HeLa. In H1299 cells, overexpression of mdm2 resulted in effective protection from apoptosis. This protective effect was seen only under conditions allowing the formation of p53-Mdm2 complexes. In contrast, excess mdm2 failed to abolish p53-mediated apoptosis in HeLa cells, despite a complete abrogation of p53-dependent sequence-specific transcriptional activation (SST). These data strongly support the contention that SST is dispensable for at least some types of p53-mediated apoptosis. Further, they suggest that one of the roles of mdm2 may be to modulate the apoptotic activity of p53, in a manner which is dictated by the pathway through which p53 induced apoptosis in a given cell type
在两种人源细胞系H1299和HeLa中研究了过量mdm2对p53介导的细胞凋亡的影响。在H1299细胞中,mdm2的过表达导致有效抵御细胞凋亡。仅在允许形成p53-Mdm2复合物的条件下才观察到这种保护作用。相比之下,尽管p53依赖性序列特异性转录激活(SST)完全消除,但过量的mdm2未能消除HeLa细胞中p53介导的细胞凋亡。这些数据有力地支持了以下论点:SST对于至少某些类型的p53介导的细胞凋亡是可有可无的。此外,它们表明mdm2的作用之一可能是以由p53在给定细胞类型中诱导细胞凋亡的途径所决定的方式来调节p53的凋亡活性。