Wang Ping, Yan Hui, Li Ji-Cheng
Institute of Cell Biology, Zhejiang University, Hangzhou 310058, PR China.
Biochem Biophys Res Commun. 2007 Nov 9;363(1):101-5. doi: 10.1016/j.bbrc.2007.08.141. Epub 2007 Aug 31.
Bcl-2 plays a pivotal role in the control of cell death and is down-regulated in trichosanthin (TCS)-induced cell apoptosis. Because Bcl-2 expression is regulated by the transcription factor cyclic AMP response element-binding protein (CREB), we investigated the role of CREB activation in TCS-induced Hela cells apoptosis. Our results showed that TCS-caused Hela cell apoptosis was accompanied by the decrease of Bcl-2 and phosphorylated CREB protein levels. Interesting, this inhibitive effect can be abolished by the combined treatment of TCS/cAMP agonists. Furthermore, TCS-mediated Bcl-2 protein was abrogated by the suppression of CREB expression with antisense treatment, and blocking the interaction between CREB-binding protein and the Bcl-2 cyclic AMP-responsive element (CRE) by a CRE decoy oligonucleotide. Therefore, these data support the hypothesis that CREB plays a critical role in the regulation of Bcl-2 expression in TCS-induced Hela cell death.
Bcl-2在细胞死亡调控中起关键作用,且在天花粉蛋白(TCS)诱导的细胞凋亡中表达下调。由于Bcl-2的表达受转录因子环磷酸腺苷反应元件结合蛋白(CREB)调控,我们研究了CREB激活在TCS诱导的Hela细胞凋亡中的作用。我们的结果表明,TCS诱导的Hela细胞凋亡伴随着Bcl-2和磷酸化CREB蛋白水平的降低。有趣的是,这种抑制作用可通过TCS/cAMP激动剂联合处理而消除。此外,通过反义处理抑制CREB表达,以及用CRE诱饵寡核苷酸阻断CREB结合蛋白与Bcl-2环磷酸腺苷反应元件(CRE)之间的相互作用,可消除TCS介导的Bcl-2蛋白。因此,这些数据支持了CREB在TCS诱导的Hela细胞死亡中对Bcl-2表达调控起关键作用这一假说。