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中国临床药理学与治疗学 ›› 2020, Vol. 25 ›› Issue (5): 489-497.doi: 10.12092/j.issn.1009-2501.2020.05.002

• 基础研究 • 上一篇    下一篇

妊娠期糖尿病中患者miR-138-5p通过调控缺氧诱导因子1α保护β细胞功能

黄好1, 肖芳2, 贾虹1, 王晓霜1, 段亚亭1   

  1. 1重庆市中医院妇产科,重庆 400021;
    2重庆市中医院 超声科,重庆 400021
  • 发布日期:2020-07-06
  • 通讯作者: 肖芳,女,本科,主治医师,研究方向:妇产科超声、腹部超声。Tel: 13272782919 E-mail: howardfine@163.com
  • 作者简介:黄好,女,本科,主治医师,研究方向:生殖医学、盆底康复。Tel: 18149916620 E-mail: dempseywell@163.com

miR-138-5p protects β cell function by regulating HIF-1α in gestational diabetes mellitus

HUANG Hao1, XIAO Fang2, JIA Hong1, WANG Xiaoshuang1, DUAN Yating1   

  1. 1 Chongqing Traditional Chinese Medicine Hospital, Chongqing Department of Gynecology and Obstetrics 400021;
    2 Department of ULtrasound, Chongqing Traditional Chinese Medicine Hospital, Chongqing 400021, China
  • Published:2020-07-06

摘要: 目的:探讨在妊娠期糖尿病(GDM)患者中miR-138-5p对胰岛β细胞功能的影响及其相关作用机制。方法:通过RT-qPCR对比15例GDM患者与15例的正常健康孕妇外周血中miR-138-5p的表达差异;miR-138-5p mimic及inhibitor分别转染入β细胞系INS-1细胞中,过表达或抑制其在该细胞中的表达水平,并通过RT-qPCR验证转染效率;利用MTT增殖实验、Annexin V-FITC凋亡实验及胰岛素释放实验分别检测miR-138-5p对INS-1细胞的增殖、凋亡和胰岛素释放能力的影响;通过miRNA靶基因预测软件TargetScan筛选miR-138-5p的目标靶基因,并利用双荧光素酶基因报告及Western blot实验进行验证;功能挽救实验证实miR-138-5p是否通过靶向调控其目标基因而发挥对INS-1细胞的增殖、凋亡及胰岛素释放能力影响;Western blot实验检测miR-138-5p在INS-1细胞中作用的分子信号通路。结果:与正常健康孕妇相比,GDM患者外周血中miR-138-5p的表达显著低表达;在INS-1细胞中转染miR-138-5p mimic及inhibitor后可显著促进或抑制miR-138-5p的表达;过表达miR-138-5p可明显促进INS-1细胞的增殖,抑制其发生凋亡并促进细胞对胰岛素的释放能力;而下调miR-138-5p的表达,可显著抑制INS-1细胞的增殖,促进其发生凋亡及抑制细胞的胰岛素释放能力;通过miRNA靶基因预测软件TargetScan筛选缺氧诱导因子1α(hypoxia-inducible factor-1α, HIF-1α)为miR-138-5p的目标靶基因,双荧光素酶基因报告实验及Western blot实验提示miR-138-5p可抑制INS-1细胞中HIF-1α的表达;功能挽救实验证实miR-138-5p通过调控HIF-1α的表达,影响INS-1细胞的增殖、凋亡及胰岛素释放能力;Western blot实验明确miR-138-5p可能通过靶向调控HIF-1α的表达,影响PI3K/AKT信号通路中PI3K、AKT及其磷酸化后的p-PI3K、p-AKT蛋白而发挥对INS-1细胞的作用。结论:在GDM患者中,miR-138-5p可能通过靶向调控HIF-1α的表达,进而影响PI3K/AKT信号通路,促进β细胞的增殖、抑制其凋亡,并促进其胰岛素释放能力从而保护β细胞的功能。

关键词: 妊娠期糖尿病, miR-138-5p, HIF-1α, INS-1细胞, PI3K/AKT信号通路

Abstract: AIM: To study the effect of miR-138-5p on the function of β cell in gestational diabetes mellitus (GDM) and its related mechanism. METHODS: The expression of miR-138-5p in peripheral blood of 15 GDM pregnant women and 15 normal pregnant women were compared by RT-qPCR. miR-138-5p mimic and inhibitor were transfected into INS-1 cells, respectively, and their expression level was over expressed or inhibited. RT-qPCR was used to verify the transfection efficiency.MTT proliferation experiment, Annexin V-FITC apoptosis experiment and insulin release experiment were used to detect the effects of miR-138-5p on INS-1 cell proliferation, apoptosis and insulin release ability. The target gene of miR-138-5p was screened by TargetScan, a miRNA target gene prediction software. The functional rescue experiment confirmed whether miR-138-5p could exert its influence on INS-1 cell proliferation, apoptosis and insulin release ability by targeting its target gene. Western blot was used to detect the molecular signaling pathway of miR-138-5p in INS-1 cells. RESULTS: The expression of miR-138-5p in peripheral blood of GDM pregnant women was significantly lower than that of normal pregnant women. RT-qPCR showed that miR-138-5p mimic and inhibitor could significantly promote or inhibit the expression of miR-138-5p in INS-1 cells. The results of MTT proliferation experiment, Annexin V-FITC apoptosis experiment and insulin release experiment indicated that over expression of miR-138-5p could significantly promote the proliferation of INS-1 cells, inhibit the apoptosis of cells and promote the insulin release ability of cells. However, down-regulating the expression of miR-138-5p could significantly inhibit the proliferation of INS-1 cells, promote apoptosis and inhibit insulin release. HIF-1α was selected as the target gene of miR-138-5p by TargetScan. The double luciferase gene report and Western blot showed that miR-138-5p could inhibit the expression of HIF-1α in INS-1 cells. The functional rescue experiment confirmed that miR-138-5p could affect the proliferation, apoptosis and insulin release of INS-1 cells by regulating the expression of HIF-1α. Western blot showed that miR-138-5p may play a role in INS-1 cells by affecting PI3K, Akt and p-PI3K, p-Akt protein after phosphorylation in PI3K/Akt signaling pathway. CONCLUSION: miR-138-5p may reguLate HIF-1α expression in a targeted manner, thereby affecting the PI3K/AKT signaling pathway, promoting the proliferation and inhibition of the parent cells' apoptosis, and promoting their insulin-releasing ability to protect the function of β cell in GDM.

Key words: gestational diabetes mellitus, miR-138-5p, HIF-1 α, INS-1 cells, PI3K/Akt signaling pathway

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