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机构地区:[1]安徽医科大学第一附属医院血液内科,合肥230022
出 处:《安徽医科大学学报》2014年第8期1080-1084,共5页Acta Universitatis Medicinalis Anhui
基 金:安徽省高等学校省级自然科学研究重点项目(编号:KJ2011A164)
摘 要:目的研究高三尖杉酯碱(HHT)作用于急性单核细胞白血病(AML-M5)SHI-1细胞株的机制,是否可抑制SHI-1细胞的增殖、诱导细胞凋亡;了解HHT对AML-M5 SHI-1细胞膜电位的影响,即其诱导的细胞凋亡是否通过线粒体介导的细胞凋亡途径实现。方法将不同浓度(5、10、50、100、500μg/L)的HHT作用SHI-1细胞,瑞氏染色观察细胞镜下形态学改变、流式细胞术AnnexinV-FITC/PI法检测细胞凋亡、CCK-8法测细胞增殖抑制作用、线粒体膜电位试剂盒(线粒体染料JC-1活细胞染色)检测线粒体跨膜膜电位(Δψm)变化。结果 HHT能有效抑制SHI-1细胞的增殖、诱导其凋亡,随着药物浓度的增高,细胞凋亡率、增殖抑制率明显增加(P<0.05)。流式细胞仪线粒体膜电位结果表明,HHT作用后存在明显荧光变化,细胞线粒体膜电位下降,并呈浓度相关性。结论 HHT可抑制AML-M5 SHI-1细胞株的增殖、诱导其凋亡,其诱导细胞凋亡可能是通过线粒体介导的细胞凋亡途径实现。Objective To explore the effect of homoharringtonine (HHT) on proliferation and induce apoptosis of acute monocytic leukemia cell line SHI-1,and whether the induction of apoptosis is mediated by mitochondrial apoptosis pathway.Methods Experiments were divided into control and test groups (5,10,50,100,500 μg/L).The growth inhibitory rate of SHI-1 cells was detected using Cell Counting Kit-8 (CCK-8) method,while the cell apoptotic rate was measured by AnnexinV-FITC/PI using flow cytometry.Mitochondrial membrane potential across the membrane(△ψm) was determined by mitochondrial membrane potential assay kit with JC-1.Results HHT inhibited the growth of SHI-1 cells and induced apoptosis in concentration-dependent manners (P < 0.05).Mitochondrial membrane potential across the membrane analysis showed that SHI-1 cells significantly showed an alteration of fluoresence after treating with HHT for 20 hours,as compared with control group.Conclusion HHT is able to inhibit proliferation and induce apoptosis of SHI-1 cells,the mechanism may be associated with the mediation by mitochondrial apoptosis pathway.
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