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七叶皂苷钠通过抑制Akt和ERK信号通路诱导HeLa细胞凋亡及对死亡受体表达的影响
引用本文:齐世美,戚之琳,凌烈锋,吕俊,章尧.七叶皂苷钠通过抑制Akt和ERK信号通路诱导HeLa细胞凋亡及对死亡受体表达的影响[J].中国病理生理杂志,2014,30(2):239-244.
作者姓名:齐世美  戚之琳  凌烈锋  吕俊  章尧
作者单位:皖南医学院生物化学教研室, 安徽 芜湖 241002
基金项目:国家自然科学基金资助项目(No. 31301171);活性生物大分子研究安徽省重点实验室项目(No. 1306C083008);高等学校省级优秀青年人才基金重点项目(No.2013SQRL055ZD);皖南医学院博士科研启动基金资助项目
摘    要: 目的:探讨七叶皂苷钠诱导宫颈癌HeLa细胞凋亡的作用及其分子机制。方法:采用MTT法检测七叶皂苷钠对宫颈癌HeLa细胞的生长和增殖抑制作用;倒置显微镜观察细胞形态改变;利用annexin V-FITC/PI流式细胞术检测细胞凋亡率;采用DAPI单染法荧光显微镜下观察细胞核变化情况; 利用Western blotting检测凋亡相关蛋白[聚(ADP-核糖)聚合酶(PARP)、cleaved caspase-8、cleaved caspase-9、pro-caspase-3]和细胞存活相关信号通路(Akt、ERK)以及TRAIL受体(DR4、DR5)的变化情况。结果:七叶皂苷钠以剂量依赖的方式显著抑制宫颈癌HeLa细胞的生长和增殖;七叶皂苷钠作用于HeLa细胞后,可见典型的凋亡细胞形态学特征,细胞凋亡率显著增加;随着七叶皂苷钠浓度升高,cleaved PARP、cleaved caspase-8和cleaved caspase-9明显增多,pro-caspase-3显著减少,p-Akt和p-ERK激活减少,细胞内DR4和DR5总蛋白水平上调。结论:七叶皂苷钠通过抑制细胞存活相关信号通路,上调死亡受体水平,抑制细胞增殖,促进细胞凋亡。

关 键 词:七叶皂苷钠  宫颈肿瘤  细胞凋亡  死亡受体  Akt通路  ERK通路  
收稿时间:2013-10-10

Sodium aescinate induces apoptosis of HeLa cells by inhibiting Akt/ERK signaling pathways and increasing death receptor expression
QI Shi-mei,QI Zhi-lin,LING Lie-feng,L Jun,ZHANG Yao.Sodium aescinate induces apoptosis of HeLa cells by inhibiting Akt/ERK signaling pathways and increasing death receptor expression[J].Chinese Journal of Pathophysiology,2014,30(2):239-244.
Authors:QI Shi-mei  QI Zhi-lin  LING Lie-feng  L Jun  ZHANG Yao
Institution:Department of Biochemistry, Wannan Medical College, Wuhu 241002, China.
Abstract:AIM:To study the effects of sodium aescinate on the apoptosis of cervical cancer HeLa cells and its molecular mechanism. METHODS:MTT assay was used to detect the growth and proliferation of HeLa cells. The morphological alteration was observed under inverted microscope. Annexin V-FITC/PI double staining and DAPI nuclear staining were used to determine the apoptosis of HeLa cells induced by sodium aescinate. The apoptosis-related proteins PARP, cleaved caspase-8 and pro-caspase-3, and the proliferation-associated molecules Akt and ERK, as well as TRAIL receptors DR4 and DR5 were detected by Western blotting. RESULTS:Sodium aescinate inhibited the growth of HeLa cells in a concentration-dependent manner. Treatment with sodium aescinate induced the typical morphology of apoptotic cells and increased the apoptotic rate significantly. The cleaved PARP, cleaved caspase-8 and cleaved caspase-9 protein expression was observed. The expression of DR4 and DR5 was up-regulated. Meanwhile, pro-caspase-3 was decreased, and the levels of p-Akt and p-ERK were down-regulated by sodium aescinate in a dose-dependent manner. CONCLUSION:Sodium aescinate inhibits the proliferation and promotes the apoptosis of HeLa cells by increasing death receptor expression and repressing proliferation-associated signaling pathways.
Keywords:Sodium aescinate  Uterine cervical neoplasms  Apoptosis  Death receptors  Akt pathway  ERK pathway
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