临床荟萃 ›› 2020, Vol. 35 ›› Issue (12): 1093-1096.doi: 10.3969/j.issn.1004583X.2020.12.006

• 论著 • 上一篇    下一篇

miR-16 在冠心病患者血清中表达及功能分析

  

  1. 1.隆尧县医院检验科,河北 邢台  055350;2.北京大学人民医院 检验科,北京  100044
  • 出版日期:2020-12-20 发布日期:2020-11-27
  • 通讯作者: 靳星, Email:36815763@qq.com

Expression and function analysis of miR-16 in the serum of patients with coronary heart disease

  1. 1.Department of Clinical Laboratory, Longyao County Hospital, Xingtai 055350,China;
    2.Department of Clinical Laboratory, Peking University People's Hospital, Beijing 100044, China
  • Online:2020-12-20 Published:2020-11-27
  • Contact: Corresponding author: Jin Xing, Email:36815763@qq.com

摘要: 目的  探讨血浆miR16与冠心病的关系,并阐明该miR对血管平滑肌细胞增殖表型的调控作用。方法  随机选取冠心病患者43例及健康对照49例,通过实时荧光定量聚合酶链反应(PCR)检测血浆miR16的表达强度。将miR16类似物转染人血管平滑肌细胞,通过CCK8实验检测细胞的增殖活力,通过蛋白印迹检测细胞周期蛋白(cyclin) D1、D2和E1的表达。结果  冠心病患者血浆miR16表达水平显著低于对照组(P<0.05)。过表达miR16可显著抑制血管平滑肌细胞的增殖,并下调cyclin D1、D2和E1的表达。结论  miR16在冠心病患者血浆中表达降低,该miR可能通过靶向抑制细胞周期蛋白cyclinD1、D2和E1的表达抑制血管平滑肌细胞增殖。

关键词: microRNA-16, 冠状动脉疾病, 增殖, 细胞周期蛋白类

Abstract: Objective  To explore the relationship between plasma miR16 and coronary heart disease(CHD), and to clarify the regulation of miR16 on the proliferation phenotype of vascular smooth muscle cells. Methods  Fortythree patients with coronary heart disease and 49 healthy volunteers were randomly selected. The expression intensity of plasma miR16 was detected by realtime fluorescent quantitative polymerase chain reaction (PCR). miR16 analogues were transfected into human vascular smooth muscle cells, and the proliferation activity of the cells was detected by CCK8 experiment. The expression of cyclin D1, D2 and E1 were detected by western blot. Results  The expression of plasma miR16 in CHD patients was significantly lower than that in  control group(P<0.05). Overexpression of miR16 significantly inhibited the proliferation of vascular smooth muscle cells and downregulated the expression of cyclin D1, D2 and E1. Conclusion  miR16 expression was decreased in plasma of patients with CHD. This miR may inhibit the proliferation of vascular smooth muscle cells through targeting the expression of cyclin D1, D2 and E1.

Key words: microRNA-16, coronary disease, proliferation, cyclins

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