普罗布考抑制大鼠血管平滑肌细胞周期素D1蛋白表达和G1→S转换
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国家自然科学基金(30171084)资助;国家973子项目(G2000056905)资助


Probucol Reduces Cyclin D1 Protein Expression and G1→S Transition in Rat Vascular Smooth Muscle Cells
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    摘要:

    目的研究普罗布考是否通过阻滞细胞周期抑制平滑肌细胞增殖。方法首先用普罗布考和氧化型低密度脂蛋白与平滑肌细胞共同孵育。然后用MTT法和细胞计数法测定细胞增殖,用流式细胞术观察细胞周期,最后用蛋白印迹测蛋白表达。结果MTT法和细胞计数法显示25~100 mg/L氧化型低密度脂蛋白都能刺激平滑肌细胞增殖,效应呈浓度依赖性,普罗布考能显著抑制氧化型低密度脂蛋白所诱导的细胞增殖,效应呈浓度和时间依赖性。流式细胞术分析表明普罗布考增加了G0/G1细胞比例达28.6%(p<0.01,n=3),减少S期细胞比例达83.5%(p<0.01,n=3)。蛋白印迹结果显示氧化型低密度脂蛋白诱导细胞周期素D1蛋白表达,高峰在6~12 h,普罗布考显著减少周期素D1蛋白表达,在6 h和12 h分别减少达26%和23%(P均<0.01,n=3)。结论普罗布考显著抑制氧化型低密度脂蛋白所诱导的细胞增殖,其抗增殖活性与普罗布考下调周期素D1蛋白表达,从而阻滞细胞由G0/G1期向S期转换有关。

    Abstract:

    Aim To examine whether procucol could inhibit vascular smooth muscle cells(VSMC) proliferation by impairing cell cycle progression. Methods Initially,quiescent rat VSMC were treated with probucol in the presence of oxidized low density lipoprotein(ox-LDL).Then cell proliferation was measured by MTT assay and cell counts,and cell cycle distribution was analyzed by Flow-cytometry(FCM).Finally,protein expression was examined by western blot. Results MTT assay and cell counts revealed that 25 mg/L,50 mg/L and 100 mg/L ox-LDL stimulated VSMC proliferation in a dose dependent manner.Probucol significantly inhibited VSMC proliferation induced by ox-LDL in a dose and time dependent manner.FCM analysis showed that probucol increased cells in G0/G1 by 28.6%(p<0.01,n=3),reduced the cells in S by 83.5%(p<0.01,n=3).Also,100 mg/L oxLDL induced cyclin D1 expression,with peak in 6~12 h.Probucol markedly inhibited cyclin D1 expression by 26% at 6 h and 23% at 12 h respectively(both p<0.01,n=3). Conlusions Probucol significantly inhibits ox-LDL induced VSMC proliferation.This antiproliferative effect of probucol is correlated with suppression of cell progression by blocking the cell cycle in G0/G1.Furthermore,suppression of cell cycle progression is associated with the down-expression of cyclin D_1 protein by probucol

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涂永生,,严鹏科,朱炳阳,黄红林,廖端芳.普罗布考抑制大鼠血管平滑肌细胞周期素D1蛋白表达和G1→S转换[J].中国动脉硬化杂志,2005,13(6):676~679.

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  • 收稿日期:2005-06-27
  • 最后修改日期:2005-09-29
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