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作 者:刘丹莉[1] 杨云华[1] 于小华[1] 李双杰[1]
出 处:《陕西医学杂志》2010年第3期259-262,共4页Shaanxi Medical Journal
基 金:国家自然科研基金资助项目(30271665);湖南省教育厅科研基金资助项目(C5C458)
摘 要:目的:观察黄芪甲甙(AST)对小鼠骨髓间充质干细胞(BMSCs)凋亡的影响。方法:从Balb/c小鼠股骨骨髓中提取BMSCs并鉴定,加入阿霉素(ADR)(10μg/L)诱导BMSCs凋亡,同时加入不同剂量的MR与BMSCs共培养24h,实验共分6组,即空白对照组,ADR组、ADR+AST(4μg/L、40μg/L、400μg/L)组、MR400μg/L组。采用TUNEL法和流式细胞仪检测细胞凋亡的情况。结果:TUNEL和流式结果表明黄芪甲甙有抑制BMSCs凋亡的作用,40μg/L组作用较强,与ADR组比较差异有显著性,增加浓度抑制凋亡的作用增加不明显,ADR+AST(40μg/L、400μg/L)两组,细胞凋亡率差异无显著性。结论:黄芪甲甙具有抑制阿霉素诱导的骨髓间充质干细胞凋亡的作用,无剂量依赖性。Objective:To determine the effect of astragaloside on the apoptosis of mesenchymal stem cells(BMSCs)induced by adriarnycinin vitro.Methods:From Balb/c mouse femur bone marrow extracted and identified BMSCs adding ADR(Adriamycin,ADR)(10μg/L)induced apoptosis BMSCs at the same time with different doses of BMSCs with AST co-culture 24h,the trial is divided into six groups,That is,the control group,ADR group,ADR + AST(4μg/L,40μg/L,400μg/L)group,MR400μg/L group.TUNELL using flow cytometry and apoptosis.Results:TUNEL-flow and the results have shown that astragalus BMSCs inhibit apoptosis,40μg/L the role of a strong group,compared with the ADR silk there was a significant difference,to increase the role of apoptosis inhibitory concentration was not obvious to increase,ADR + AST(40μg/L,400μg/L)two groups,the rate of apoptosis was no significant difference.Conclusion:Astragalus with adriamycin-induced suppression of bone marrow mesenchymal stem cells apoptosis,and no dose-dependent.
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