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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》2013年第1期12-15,共4页Acta Universitatis Medicinalis Anhui
摘 要:目的探讨黄芪总苷(AST)诱导人急性早幼粒细胞白血病细胞株NB4凋亡过程中死亡受体通路的各分子变化,以说明AST是否依赖死亡受体通路参与NB4细胞凋亡发生。方法不同浓度AST(200、300、400μg/ml)处理NB4细胞48 h后,RT-PCR法检测IKKβ、IκBα、NF-κBp65及Fas的mRNA表达变化,比色法检测caspase-8的相对活性。结果不同浓度的AST能够引起IκBαmRNA表达上调、NF-κBp65 mRNA表达下调,caspase-8活性的升高,而IKKβ及Fas的mRNA表达无明显变化。结论 AST诱导NB4细胞凋亡,可能与死亡受体通路上IκBαmRNA表达上调、NF-κBp65 mRNA表达下调,caspase-8活性升高有关。Objective To investigate whether the mechanism of the astragalosides-induced apoptosis in the acute promyelocytic leukemia cell line NB4 associates with activation of the death receptor pathway.Methods NB4 cells were treated with different concentration(200,300,400 μg/ml) of astragalosides for 48 h.The mRNA expression of gene IKKβ,IκBα,NF-κBp65,Fas and the relative activity of caspase-8 were detected by RT-PCR method and chromatometry assay respectively.Results The expression of gene IκBα was up-regulated while gene NF-κBp65 was down-regulated and the expression of gene IKKβ,Fas were not changed obviously.And the astragalosides-induced apoptosis involved in promotion of the relative activity of caspase-8.Conclusion The molecular mechanism of the astragalosides-induced apoptosis in NB4 cells may be associated with regulating of the expression of IκBα,NF-κBp65 mRNA and promotion of the relative activity of caspase-8 that indicates activation of the death receptor pathway.
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