实用医学杂志 ›› 2020, Vol. 36 ›› Issue (20): 2763-2768.doi: 10.3969/j.issn.1006⁃5725.2020.20.004

• 基础研究 • 上一篇    下一篇

miRNA⁃330⁃3p/Ap2m1轴在过表达GATA⁃4骨髓间充质干细胞外泌体抗心肌细胞凋亡中的作用

贺继刚1 王梓豪1 李敏1 谢巧丽1 毛富刚2   

  1. 云南省第一人民医院,昆明理工大学附属医院1心脏大血管外科,2 心血管内科(昆明650032)
  • 出版日期:2020-10-20 发布日期:2020-10-25
  • 通讯作者: 毛富刚E⁃mail:jiganghe999@163.com
  • 基金资助:

    国家自然科学基金(编号:81460073);云南省科技厅⁃昆明医科大学应用基础研究联合专项[编号:2014FB089,2019FE001(⁃120)];云南省教育厅科学研究基金(编号:2015Z051);中国博士后科学基金(编号:2015M582764XB);成都医学院2015年度科研项目(编号:CYZ15⁃18);云南省医学后备人才(编号:H⁃201607);云南省青年拔尖人才项目


Role of the miRNA⁃330⁃3p/Ap2m1 axis in the overexpression of GATA⁃4 bone marrow mesenchymal stem cell exosomes in anti ⁃ cardiomyocyte apoptosis

HE Jigang*,WANG Zihao,LI Min,XIE Qiaoli,MAO Fu⁃gang.#br#   

  1. *Department of Cardiovascular Surgery,the First People′s Hospital of Yunnan Province,the Affiliated Hospital of Kunming University of Science and Technology,Kunming 650032,China
  • Online:2020-10-20 Published:2020-10-25
  • Contact: MAO Fugang E⁃mail:jiganghe999@163.com

摘要:

目的 探讨过表达GATA⁃4小鼠骨髓间充质干细胞(BMSC)分泌外泌体(BMSC^GATA⁃4exosome)通过miRNA⁃330⁃3p/Ap2m1轴减少心肌细胞凋亡,提高心肌梗死心功能。方法 建立小鼠心梗模型,共分7组分别经尾静脉注射BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome、BMSC^miRNA⁃330⁃3p⁃inhibitor⁃exosome、BMSC^GATA⁃4⁃exosome、BMSC^空载体⁃exosome、BMSCexosome 48 h,同时将心梗未处理组及正常小鼠作为对照组。采用心脏彩超检测各组心功能,RT⁃PCR检测心梗心肌细胞内miRNA⁃330⁃3p的表达,Tunel法检测各组心梗心肌细胞凋亡数量。miRNA⁃330⁃3p对应靶基因Ap2m1、Cnot4蛋白采用Western blot 法进行检测。

结果 BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome组心梗心功能改善最为明显(< 0.05),其心肌细胞内miRNA⁃330⁃3p 表达量最高(< 0.05)。BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome 组心肌细胞的凋亡率最低(< 0.05)、BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome 组心梗心肌细胞内的Ap2m1 的表达最低(< 0.05)。结论 过表达GATA⁃4小鼠骨髓间充质干细胞外泌体通过miRNA⁃330⁃3p/Ap2m1轴抗心肌细胞凋亡。


关键词: miRNA?330?3p, Ap2m1蛋白, GATA?4, 外泌体, 小鼠骨髓间充质干细胞

Abstract:

Objective The research aimed to investigate the role of miRNA⁃330⁃3p/Ap2m1 axis in theeffects of reduction of myocardial cell apoptosisand improvement of myocardial function in myocardial infarctionby GATA⁃4 overexpressed⁃mouse bone marrow mesenchymal stem cell(BMSC)⁃secreted exosomes(BMSC^GATA⁃4⁃exosome). Method Mouse myocardial infarction models were established and then divided into seven groups. Eachmouse was injected with BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome,BMSC^miRNA⁃330⁃3p⁃inhibitor⁃exosome,BMSC^GATA⁃4⁃exosome,BMSC^empty carrier⁃exosome,and BMSCexosome through the caudal vein for 48 hours. The untreated myocardial infarction group andnormal mice were included in the control group. Cardiac color ultrasound was used to detect cardiac function ineach group. The expression of miRNA⁃330⁃3p in myocardial infarction was detected by RT⁃PCR. Tunel assay wasused to detect the number of apoptotic cells in myocardial tissue of myocardial infarction in each group. Westernblot was used to detect the expression of the corresponding target gene Ap2m1 of miRNA⁃330⁃3p and Cnot4 protein.Results The BMSC^miRNA⁃673⁃5p⁃mimic⁃exosome group showed the most significant improvement in myocardial function inmyocardial infarction(P < 0.05)and the highest expression of miRNA⁃330⁃3p in cardiomyocytes(P < 0.05). Thecardiomyocytes in the BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome group had the lowest apoptosis rate(P < 0.05),and Ap2m1 inthe BMSC^miRNA⁃330⁃3p⁃mimic⁃exosome+myocardial cell culture group had the lowest expression(P < 0.05). Conclusion Overexpressed GATA⁃4 bone marrow⁃derived mesenchymal stem cell exosomes inhibit the expression of Ap2m1protein against myocyte apoptosis through miRNA⁃330⁃3p.

Key words: miRNA?330?3p, Ap2m1 protein, GATA?4, exosome, mouse bone marrow?derived mesenchymal stem cells