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首页|期刊导航|山东医药|miR-206对高磷诱导大鼠血管平滑肌细胞钙化的影响及机制

miR-206对高磷诱导大鼠血管平滑肌细胞钙化的影响及机制

邵娟 吴基良 李敏才

山东医药2016,Vol.56Issue(21):10-12,3.
山东医药2016,Vol.56Issue(21):10-12,3.DOI:10.3969/j.issn.1002-266X.2016.21.004

miR-206对高磷诱导大鼠血管平滑肌细胞钙化的影响及机制

Effect of miR-206 on high phosphorus-induced calcification in rat vascular smooth muscle cells

邵娟 1吴基良 1李敏才1

作者信息

  • 1. 湖北科技学院,湖北咸宁 437100
  • 折叠

摘要

Abstract

Objective To investigate the effect of microRNA-206 (miR-206)on β-glycerophosphate (β-GP)-in-duced calcification in rat vascular smooth muscle cells (VSMCs).Methods Aortal VSMCs were primarily cultured and i-dentified in vitro.VSMCs were divided into five groups:control group,mimics negative control group,miR-206 mimic group,inhibitor negative control group and miR-206 inhibitor group.Each group was transfected by lipofectamine2000.Af-ter 48-hour transfection,each group was stimulated with 10 mmol/Lβ-GP to induce calcification of VSMCs.Observing cal-cium deposition with Alizarin red staining while detecting the alkaline phosphate (ALP)activity and the expression of con-nexin 43 (Cx-43)respectively by Trace enzyme standard method and immunofluorescence method after induction for 4 days.Results After transfection 48 h,VSMCs were treated with β-GP for 4 days.Compared with the negative control group,the calcium deposition decreased in the miR-206 mimic group and increased in the miR-206 inhibitor group;the ALP activity and the expression of Cx43 decreased in the miR-206 mimic group and increased in the miR-206 inhibitor group (all P <0.05).Conclusions miR-206 may inhibit β-GP-induced calcification of VSMCs by regulating Cx43.

关键词

微小RNA-206/β-甘油磷酸钠/血管平滑肌细胞/钙化/大鼠

Key words

microRNA-206/β-glycerophosphate/vascular smooth muscle cells/calcification/rats

分类

医药卫生

引用本文复制引用

邵娟,吴基良,李敏才..miR-206对高磷诱导大鼠血管平滑肌细胞钙化的影响及机制[J].山东医药,2016,56(21):10-12,3.

基金项目

国家自然科学基金资助项目(81270355);湖北省自然科学基金资助项目(2014CFB211)。 ()

山东医药

OA北大核心CSTPCD

1002-266X

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