Zhang Ya-hong, Guo Jing-gong, Guo Zi-hua, Xie Song-qiang
Key Laboratory of Natural Medicine and Immuno-Engineering of Henan University, Kaifeng 475004, China.
Yao Xue Xue Bao. 2011 Nov;46(11):1332-7.
This paper is to report the study of resveratrol-induced apoptosis and its mechanisms in MCF-7 cells. MTT assay was performed to assess the cytotoxicity of resveratrol on MCF-7 cells. Hoechst 33258 staining was used to observe cellular morphologic changes in apoptosis. Apoptosis was measured by flow cytometric analysis and the protein expression was examined by Western blotting analysis. The results indicated that resveratrol could inhibit MCF-7 cell growth in a time- and concentration-dependent manner. Remarkable morphologic changes in the cells after 60 micromol L(-1) resveratrol treatment, including cell nuclear shrinkage, DNA condensation and apoptotic bodies, were observed by Hoechst 33258 staining. Resveratrol could induce apoptosis and activate p38 and p53 in a time dependent manner in MCF-7 cells. In addition, the cell growth inhibitory ratio and the apoptotic ratio of resveratrol-treated group decreased markedly by the p38 MAPK inhibitor SB203580 or p53 inhibitor pifithrin-alpha. Further experiments confirmed that resveratrol-induced p53 activation was reduced by SB203580 whereas the activation of p38 was not affected by pifithrin-alpha. In conclusion, resveratrol induced apoptosis in MCF-7 cells could be through activating p38-p53 signal pathway.
本文旨在报道白藜芦醇诱导MCF - 7细胞凋亡及其机制的研究。采用MTT法评估白藜芦醇对MCF - 7细胞的细胞毒性。用Hoechst 33258染色观察细胞凋亡的形态学变化。通过流式细胞术分析检测细胞凋亡情况,并用蛋白质印迹分析检测蛋白质表达。结果表明,白藜芦醇能以时间和浓度依赖性方式抑制MCF - 7细胞生长。用Hoechst 33258染色观察到,60 μmol L(-1)白藜芦醇处理后细胞出现明显的形态学变化,包括细胞核收缩、DNA浓缩和凋亡小体。白藜芦醇能在MCF - 7细胞中以时间依赖性方式诱导细胞凋亡并激活p38和p53。此外,p38 MAPK抑制剂SB203580或p53抑制剂pifithrin - α可使白藜芦醇处理组的细胞生长抑制率和凋亡率显著降低。进一步实验证实,SB203580可降低白藜芦醇诱导的p53激活,而pifithrin - α不影响p38的激活。总之,白藜芦醇诱导MCF - 7细胞凋亡可能是通过激活p38 - p53信号通路实现的。