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首页> 外文期刊>藥學雜誌 >Effect of delta-elemene on Hela cell lines by apoptosis induction.
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Effect of delta-elemene on Hela cell lines by apoptosis induction.

机译:δ-榄香烯通过诱导细胞凋亡对Hela细胞系的影响。

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摘要

This study was designed to investigate the apoptosis-inducing activity of delta-elemene on Hela cells in vitro. MTT assay and Hoechst 33258/PI fluorescence microscopy were used for this investigation. Apoptosis was further confirmed and quantified by DNA fragmentation ELISA, Annexin V (AnV) binding of externalized phosphatidylserine and the mitochondrial probe JC-1 using flow cytometry. Generation of reactive oxygen species (ROS) was detected using CM-H2DCFDA. Western blots analysis was performed using antibodies against the pro-caspase-3, or PRAP (Poly (ADP-ribose) polymerase).The results showed that delta-elemene exhibited a marked antiproliferative effect on Hela cells in dose- and time-dependent manners, and had little inhibition to normal human liver cell line WRL-68. It was demonstrated that delta-elemene was capable of inducing DNA fragmentation in a dose- and time-dependent manner. AnV positivity and the disturbance of the polarized mitochondrial transmembrane potential (Deltapsim) suggested that delta-elemene induced apoptotic death of Hela cells. Western blot analysis demonstrated that delta-elemene activated the caspase-signaling pathway, leading to the proteolysis conversion of pro-caspase-3 to activate caspase-3, and the subsequent cleavage of the caspase substrate PARP. Further, it was noted that the apoptotic effect of delta-elemene could be attenuated by L-Glutathione (GSH) or z-DEVD-fmk. It suggested that the increase in ROS generation might be involved in the mechanism of delta-elemene induced cell apoptosis.
机译:本研究旨在研究δ-榄香烯在体外对Hela细胞的凋亡诱导活性。使用MTT测定法和Hoechst 33258 / PI荧光显微镜进行这项研究。使用流式细胞仪通过DNA片段酶联免疫吸附测定,膜联蛋白V(AnV)与外部化磷脂酰丝氨酸和线粒体探针JC-1的结合进一步证实并量化了细胞凋亡。使用CM-H2DCFDA检测了活性氧(ROS)的生成。使用针对pro-caspase-3或PRAP(聚(ADP-核糖)聚合酶)的抗体进行了蛋白质印迹分析。结果表明,δ-榄香烯对Hela细胞具有明显的抗增殖作用,呈剂量和时间依赖性。对正常人肝细胞株WRL-68几乎没有抑制作用。已证明δ-榄香烯能够以剂量和时间依赖性方式诱导DNA片段化。 AnV阳性和极化线粒体跨膜电位(Deltapsim)的干扰表明δ-榄香烯诱导Hela细胞凋亡死亡。 Western印迹分析表明,δ-榄香烯激活了caspase信号通路,导致pro-caspase-3的蛋白水解转化为激活caspase-3,并随后裂解了caspase底物PARP。此外,注意到δ-榄香烯的凋亡作用可被L-谷胱甘肽(GSH)或z-DEVD-fmk减弱。提示ROS生成的增加可能与δ-榄香烯诱导的细胞凋亡机制有关。

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