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曲欣, 李鑫, 蔡朋朋, 商潇云, 郭东北, 由娜, 李洪源. 连翘抗肿瘤活性成分体外诱导HeLa细胞凋亡作用[J]. 中国公共卫生, 2013, 29(3): 397-399. DOI: 10.11847/zgggws2013-29-03-30
引用本文: 曲欣, 李鑫, 蔡朋朋, 商潇云, 郭东北, 由娜, 李洪源. 连翘抗肿瘤活性成分体外诱导HeLa细胞凋亡作用[J]. 中国公共卫生, 2013, 29(3): 397-399. DOI: 10.11847/zgggws2013-29-03-30
QU Xin, LI Xin, CAI Peng-peng.et al, . In vitro induction of apoptosis caused by bioactive compounds extracted from Forsythia suspensa and its mechanisim in HeLa cells[J]. Chinese Journal of Public Health, 2013, 29(3): 397-399. DOI: 10.11847/zgggws2013-29-03-30
Citation: QU Xin, LI Xin, CAI Peng-peng.et al, . In vitro induction of apoptosis caused by bioactive compounds extracted from Forsythia suspensa and its mechanisim in HeLa cells[J]. Chinese Journal of Public Health, 2013, 29(3): 397-399. DOI: 10.11847/zgggws2013-29-03-30

连翘抗肿瘤活性成分体外诱导HeLa细胞凋亡作用

In vitro induction of apoptosis caused by bioactive compounds extracted from Forsythia suspensa and its mechanisim in HeLa cells

  • 摘要: 目的探讨连翘抗肿瘤活性成分LQ-4体外对人宫颈癌HeLa细胞的增殖抑制和诱导HeLa细胞凋亡及机制。方法通过水提取、醇沉、大孔吸附树脂柱层析分离、薄层层析,分离提取LQ-4;四甲基偶氮唑蓝比色法观察LQ-4对HeLa细胞增殖抑制作用;吖啶橙/溴化乙锭双荧光染色法、透射电镜观察细胞凋亡的形态学变化;western blot法测定HeLa细胞caspase-8表达水平。结果LQ-4体外对HeLa细胞的生长、增殖均有抑制作用,12、24和48 h的半数抑制浓度(IC50)分别为93.74、33.30、22.65 μg/mL;LQ-4作用HeLa细胞后,透射电镜观察可见典型凋亡细胞形态;LQ-4作用于HeLa细胞后,促进caspase-8酶原活化,在43及18 kD上均有表达。结论LQ-4对HeLa细胞的增殖具有抑制作用,可诱导HeLa细胞凋亡,其机制可能与caspase-8蛋白酶原裂解有关。

     

    Abstract: ObjectiveTo study the cell inhibitory and apoptosis effect of bioactive compounds extracted from Forsythia suspensa(LQ-4) on HeLa cells in vitro,and to study the mechanism of anti-tumor activity of LQ-4.MethodsLQ-4 was extracted by means of alcohol precipitation,macroporous resin chromatography,and thin-layer chromatography.Methyl thiazolyl tetrazolium(MTT) assay was used to evaluate the growth inhibition rate of HeLa cells treated by different concentrations of LQ-4.Arcridine orange/ethidium bromide(AO/EB) fluorescent staining and transmission electron microscopy(TEM) were used to observe cell morphology.Western blot was used to detect the cell apoptosis-related protein in HeLa cells treated by LQ-4(50 μg/ml) at different times.ResultsThe anti-tumor active components(LQ-4) showed time-dose-dependent inhibitory effect on the proliferation of HeLa cells in vitro.The concentration for 50% inhibition(IC50) at 12,24,and 48 hours was 93.74,33.30,and 22.65 μg/mL,respectively.Fluorescence microscope and TEM detection showed that HeLa cells presented characteristic morphological changes of apoptosis after LQ-4 treatment.The results of western blot revealed that LQ-4(50 μg/mL) could promote the activation of the zymogen of caspase-8.ConclusionLQ-4 has an inhibitory effect on HeLa cell proliferation and could induce HeLa cell apoptosis,which is probably related to the decomposition of caspase-8 protease.

     

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