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作 者:史新强[1] 沈业寿[1] 卫自[1] 马金宝[1]
机构地区:[1]安徽大学生命科学学院,生化微生物研究所安徽省中药研究与开发重点实验室,安徽合肥230039
出 处:《癌变.畸变.突变》2007年第6期440-443,共4页Carcinogenesis,Teratogenesis & Mutagenesis
摘 要:背景与目的:观察桑黄胞内多糖(PLIP)对体外培养的人白血病细胞K562的增殖抑制作用,并初步探讨其作用机制。材料和方法:采用MTT法及台盼蓝拒染法测定细胞增殖抑制率和生长曲线,Hoechst_PI双荧光染色,流式细胞术和DNA琼脂糖凝胶电泳检测细胞凋亡。结果:PLIP在25μg/ml、50μg/ml、100μg/ml、200μg/ml、400μg/ml、800μg/ml剂量时均能显著抑制K562细胞增殖(P<0.05),其中400μg/ml剂量时抑制率最高,达52.55%,半数抑制浓度(IC50)为262.36μg/ml,流式细胞仪检测PLIP在100μg/ml、200μg/ml、400μg/ml剂量时K562细胞凋亡率分别为5.72%、13.57%、19.39%,并能诱导K562细胞出现凋亡所具有的形态学及生化特征。结论:PLIP对体外培养的人白血病细胞K562生长增殖具有明显的抑制作用,其作用机制可能与诱导K562细胞凋亡和影响细胞周期有关。BACKGROUND & AIM: To examine the inhibitory effects of Phellinus linteus intracellular polysaccharide (PLIP) on proliferation of leukemic cell line K562, and to explore its preliminary mechanisms. MATERIALS AND METHODS: The suppression of cellular growth was detected by MTY assay and trypan blue rejection. Apoptosis was studied by using Hoechst-PI fluorescence staining, DNA agarose gel electrophoresis, and flow cytometry. RESULTS: The PLIP could significantly inhibit the proliferation of K562 cells (P 〈 0.05), and the highest inhibition rate could reach 52.55% at the dose of 400 μg/ml,IC50 was 262.36 μg/ml. The apoptosis rates for 100 μg/ml,200 μg/ml,400 μg/ml were 5.72%, 13.57%, 19.39%, respectively, and morphologic and physiologic changes of apoptosis in K562 cells were induced . CONCLUSION: PLIP could significantly inhibit proliferation of K562 cells, and the mechanism responsible for the effect might involve the induction of apoptosis and the effects on cell cycle.
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