氧化型高密度脂蛋白促进C57BL6J小鼠骨髓源性树突状细胞成熟活化
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湖南省教育厅科技项目(编号06C692)


Effects of Angiotensin Ⅱ on the Calcification in Vascular Smooth Muscle Cells and Its Signal Pathway
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    摘要:

    目的探讨氧化修饰高密度脂蛋白(oxidized high density lipoprotein,ox-HDL)对C57B/6J小鼠骨髓源性树突状细胞(bone marrowderived dendritic cells,BMDC)成熟活化的影响。方法制备C57BL/6J小鼠骨髓细胞悬液,利用动物树突状细胞专用分离液和细胞粘附性差异去除杂细胞,用rmGMCSF和rmIL-4使其分化为BMDC。经鉴定后,实验分为PBS阴性对照、HDL组(50μg/mL)、ox-HDL组(50μg/mL)和脂多糖(1μg/mL)阳性对照组。流式细胞术检测BMDC CD8....

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    Aim To clarify the effects of angiotensin Ⅱ on the calcification in rat vascular smooth muscle cells(VSMCs) and its signal transduction. Methods Calcification of cultured rat VSMCs was prepared by incubation with β-glycerophosphate.Calcification was confirmed by Von Kossa staining,and calcium content, alkaline phosphatases activity,osteocalcin and core binding factor alpha 1(Cbfa1) mRNA expression were measured. Results Angiotensin Ⅱ enhanced the increase of calcium content,alkaline phosphatases activity,osteocalcin concentration and Cbfa1 mRNA expression in calcified VSMCs(p<0.05).Angiotensin Ⅱ type 1 receptor blocker valsartan and selective protein kinase C(PKC) inhibitor inhibited the effects of angiotensin Ⅱ on vascular calcification(p<0.05). Conclusions These data suggested that β-glycerophosphate-induced calcification in VSMCs was enhanced by angiotensin Ⅱ through angiotensin Ⅱ type 1 receptor and PKC-Cbfa1 pathway.

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许增祥,杨永宗,唐雅玲,彭茜,彭旷,何钒,夏妍,李方,王双.氧化型高密度脂蛋白促进C57BL6J小鼠骨髓源性树突状细胞成熟活化[J].中国动脉硬化杂志,2007,15(7):570.

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  • 收稿日期:2006-10-08
  • 最后修改日期:2007-08-09
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