江海龙, 梁春, 任雨笙, 姜其均, 吴建祥, 吴宗贵. 通心络下调caspase-3蛋白表达及活性抑制软脂酸诱导的人外周血内皮祖细胞凋亡[J]. 心脏杂志, 2010, 22(1): 1-5.
    引用本文: 江海龙, 梁春, 任雨笙, 姜其均, 吴建祥, 吴宗贵. 通心络下调caspase-3蛋白表达及活性抑制软脂酸诱导的人外周血内皮祖细胞凋亡[J]. 心脏杂志, 2010, 22(1): 1-5.
    Tongxinluo inhibits palmitic acid-induced apoptosis of human endothelial progenitor cells by down-regulating expression and activity of caspase-3 protein[J]. Chinese Heart Journal, 2010, 22(1): 1-5.
    Citation: Tongxinluo inhibits palmitic acid-induced apoptosis of human endothelial progenitor cells by down-regulating expression and activity of caspase-3 protein[J]. Chinese Heart Journal, 2010, 22(1): 1-5.

    通心络下调caspase-3蛋白表达及活性抑制软脂酸诱导的人外周血内皮祖细胞凋亡

    Tongxinluo inhibits palmitic acid-induced apoptosis of human endothelial progenitor cells by down-regulating expression and activity of caspase-3 protein

    • 摘要: 目的: 探讨通心络 (tongxinluo,TXL)对软脂酸 (palmitic acid,PA)诱导的人外周血内皮祖细胞(endothelial progenitor cell,EPCs)凋亡及caspase-3蛋白表达和活性的影响。方法: 密度梯度离心法获取人外周血单个核细胞,培养7 d后,贴壁细胞分成7组:对照组以M199培养液培养48 h;PA各浓度组(共3组)分别用含200,400,800 μmol/L PA的M199培养液孵育48 h;通心络干预组(共3组)分别先用含100,200,400 μmol/L TXL的M199培养液干预2 h后,再加入400 μmol/L PA孵育48 h。采用流式细胞仪检测细胞凋亡率;提取细胞蛋白,采用Western blot技术检测caspase-3蛋白表达水平;采用分光光度法检测caspase-3蛋白活性水平。结果: PA呈浓度依赖性诱导EPCs凋亡;加入TXL干预,EPCs细胞凋亡率明显降低;Western blot和分光光度法检测显示,PA组EPCs的caspase-3蛋白表达及活性明显高于对照组,200和400 μmol/L TXL干预组明显低于PA组(P<0.05)。结论: PA呈浓度依赖性诱导EPCs凋亡,TXL能部分抑制PA的上述作用,其机制与下调caspase-3蛋白表达及活性有关。

       

      Abstract: AIM: To explore the effect of tongxinluo (TXL) on apoptosis, expression and activity of caspase-3 in palmitic acid (PA)-induced peripheral blood-derived human endothelial progenitor cells in vitro. METHODS: Total mononuclear cells were isolated from peripheral blood in vitro by Ficoll density gradient centrifugation and plated on fibronectin-coated culture dishes. After 7 days, the attached cells were divided into seven groups: one control group (normal cells), three PA groups [attached cells were incubated with different concentrations of PA (200, 400 and 800 mol/L) for 48 h] and three TXL groups [attached cells were incubated with different concentrations of TXL (100, 200 and 400mol/L), respectively, for 2 h before incubation with 400 μmol/L PA for 48 h]. Flow cytometry was used to detect apoptosis. Expression and activity of caspase-3 protein were detected by Western blot and spectrophotometry, respectively. RESULTS: After exposure to PA, the apoptosis rate in treatment groups was dose-dependently higher than in the control group (P<0.05). TXL was added at different concentrations before PA incubation and cells in the TXL groups (200, 400 mol/L) showed lower apoptosis rate than in PA groups (P<0.05). Expression of caspse-3 protein and activity of EPCs in TXL groups was lower than in PA groups (P<0.05). CONCLUSION: PA promotes cell apoptosis by up-regulating expression and activity of caspase-3. TXL partly inhibits the effects of PA.

       

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