茶多酚对人γδT淋巴细胞及结肠癌细胞株SW480影响.doc

茶多酚对人γδT淋巴细胞及结肠癌细胞株SW480影响.doc

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茶多酚对人γδT淋巴细胞及结肠癌细胞株SW480影响

茶多酚对人γδT淋巴细胞及结肠癌细胞株SW480影响   作者:朱月蓉, 邱红, 刘军权, 陈复兴 【摘要】 目的: 观察茶多酚对人γδT细胞杀伤肿瘤细胞活性的影响和诱导人结肠癌细胞株(SW480)凋亡和死亡的作用。方法: 在体外用不同浓度的茶多酚诱导人γδT细胞和SW480细胞株,然后测定人γδT细胞杀瘤活性和对肿瘤细胞的作用。用不同浓度的茶多酚分别诱导SW480细胞4 h后,弃含有茶多酚的培养液再继续培养24 h,然后测定其死亡和凋亡数,用γδT细胞作对照组。结果: 茶多酚浓度350 mg/L,作用γδT细胞4 h后能明显增强γδT细胞的杀伤肿瘤细胞活性,与未诱导组和其他浓度组相比,Plt;0.01;γδT细胞对经茶多酚处理后的SW480细胞杀伤活性也明显高于对照组(Plt;0.01)。各种浓度的茶多酚分别与γδT和SW480细胞作用4 h,弃诱导液再继续培养24 h后,均能诱导其死亡和凋亡,在茶多酚浓度350 mg/L、诱导时间4 h时最明显;同一浓度的茶多酚诱导SW480细胞死亡和凋亡率明显高于γδT细胞组。结论: 茶多酚在一定浓度时能明显提高γδT细胞对肿瘤的杀伤活性;经茶多酚处理的SW480细胞更易被γδT细胞杀伤。茶多酚浓度在350 mg/L时能诱导SW480细胞凋亡而对人γδT细胞无影响。 【关键词】 茶多酚; γδ淋巴细胞; SW480细胞株; 抗肿瘤活性; 凋亡   [Abstract] Objective: To observe cytotoxicity of γδT cell induced by tea polyphenols and the direct effects of tea polyphenols on human tumor cells SW480 cell strain death and apoptosis.Methods: γδT cells and SW480 cell strain were induced by tea polyphenols in vitro to examine cytotoxic activity of γδT cell and its direct effects on tumor cells. SW480 was induced by tea polyphenols continuously for 4 hours following being cultured without tea polyphenols for 24 hours, then the rate of death and apoptosis of SW480 were measured. γδT cell was used as control group. Results: Cytotoxicity of γδT cell induced by tea polyphenols with concentration of 350 mg/L was significantly higher than that of control group and other groups(Plt;0.01). Cytotoxicity of γδT cell on SW480 induced by tea polyphenols was higher than the control group(Plt;0.01).After being induced by tea polyphenols continuously for 1~8 hours following cultured without tea polyphenols for 24 hours, SW480 showed significant cell death and apoptosis in different concentration comparing with the control group. Tea polyphenols did not display significant effects on γδT cell. Conclusion: Tea polyphenols can significantly enhance cytotoxicity of γδT cell and the SW480 induced by tea polyphenols was easily killed by γδT cell. Tea polyphnols in certain concentration can induce cell death and apopto

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