国际妇产科学杂志 ›› 2019, Vol. 46 ›› Issue (4): 426-429.

• 论著 • 上一篇    下一篇

miR-18a对人正常滋养细胞中MMP-2、MMP-9表达的影响

杨洋,陈蕊,王稳莹,刘成娟   

  1. 710077 西安医学院第一附属医院妇产科(杨洋,陈蕊,王稳莹);中国人民解放军空军军医大学唐都医院妇产科(刘成娟)
  • 收稿日期:2018-11-12 修回日期:2019-03-11 出版日期:2019-08-15 发布日期:2019-08-15
  • 通讯作者: 刘成娟,E-mail:liuchengjuan@sina.com E-mail:123632654@qq.com
  • 基金资助:
    陕西省自然科学基础研究计划项目(2018JM7115);陕西省教育厅专项科研计划项目(18JK0676)

Effect of MiR-18a on the Expression of MMP-2 and MMP-9 in Human Normal Trophoblast Cells

YANG Yang,CHEN Rui,WANG Wen-ying,LIU Cheng-juan   

  1. Department of Obstetrics and Gynecology,The First Affiliated Hospital of Xi′an Medical University,Xi′an 710077,China(YANG Yang,CHEN Rui,WANG Wen-ying);Department of Obstetrics and Gynecology,Tangdu Hospital,Chinese People′s Liberation Army Air Force Military Medical University,Xi′an 710038,China(LIU Cheng-juan)
  • Received:2018-11-12 Revised:2019-03-11 Published:2019-08-15 Online:2019-08-15
  • Contact: LIU Cheng-juan,E-mail:liuchengjuan@sina.com E-mail:123632654@qq.com

摘要: 目的:研究子痫前期(pre-eclapmpsia,PE)相关微小RNA-18a(miR-18a)对人正常滋养细胞(HTR-8细胞)中基质金属蛋白酶2(MMP-2)、MMP-9的影响。方法:按照HTR-8细胞中miR-18a的表达情况分为3组(每组重复5次):miR-18a过表达组、miR-18a抑制组、阴性对照组;实时定量聚合酶链反应(RT-qPCR)检测转染后HTR-8细胞中miR-18a mRNA的表达量;RT-qPCR和蛋白质印迹(Western blotting)检测转染后HTR-8细胞中MMP-2、MMP-9 mRNA和蛋白表达量。结果:miR-18a过表达组miR-18a mRNA表达量比阴性对照组升高,miR-18a抑制组miR-18a mRNA表达量比阴性对照组降低,差异均有统计学意义(均P<0.001)。miR-18a抑制组MMP-2、MMP-9 mRNA和蛋白表达量比阴性对照组降低,差异均有统计学意义(均P<0.001)。结论:miR-18a影响人正常滋养细胞中MMP-2、MMP-9在mRNA及蛋白水平的表达,可能通过该途径参与对滋养细胞浸润能力的调控。

关键词: 微RNAs, 先兆子痫, 基质金属蛋白酶2, 基质金属蛋白酶9, 滋养细胞

Abstract: Objective:To investigate the effect of pre-eclapmsia related miR-18a on the expression of matrix metallopeptidase 2 (MMP-2) and MMP-9 in human normal trophoblast cells (HTR-8). Methods:According to the expression of miR-18a in HTR-8 cells, it was divided into 3 groups (5 times in each group): miR-18a overexpression group, miR-18a inhibition group, negative control group. Real-time quantitative polymerase chain reaction (RT-qPCR) was used to detect the expression of miR-18a mRNA in HTR-8 cells after transfection. The mRNA and protein levels of MMP-2 and MMP-9 in HTR-8 cells were detected by RT-qPCR and Western blotting after transfection. Results:The expression of miR-18a mRNA in miR-18a overexpression group was higher than that in negative control group (P<0.001). The expression of miR-18a mRNA in miR-18a inhibition group was lower than that in negative control group (P<0.001). The expression of MMP-2 and MMP-9 mRNA and protein in the miR-18a inhibition group was lower than that in the negative control group, and the difference was statistically significant (both P<0.001). Conclusions:MiR-18a could affect the expression of MMP-2 and MMP-9 in human normal trophoblast cells at mRNA and protein levels, and may be involved in the regulation of trophoblast infiltration through this pathway.

Key words: MicroRNAs, Pre-eclampsia, Matrix metalloproteinase 2, Matrix metalloproteinase 9, Trophoblastic cell