基础医学与临床 ›› 2020, Vol. 40 ›› Issue (2): 209-214.

• 研究论文 • 上一篇    下一篇

TRPM7干扰载体修复低氧/复氧致大鼠心肌细胞系H9C2损伤

杨崛圣1, 樊虎熊3, 胡姗2, 高日峰3, 卢飞4, 王恒5, 唐燕华1*   

  1. 1.南昌大学第二附属医院 心脏大血管外科, 江西 南昌 330031;
    2.南昌大学第二附属医院 麻醉科, 江西 南昌 330031;
    3.南昌大学第二附属医院 南昌大学研究学院医学部, 江西 南昌 330031;
    4.南昌大学第二附属医院 南昌大学第二附属医院 介入室, 江西 南昌 330031;
    5.平顶山市第二人民医院 胸心外科,河南 平顶山 467000
  • 收稿日期:2019-05-20 修回日期:2019-06-26 出版日期:2020-02-05 发布日期:2020-02-05
  • 通讯作者: *tyh8565@163.com

TRPM7 interference vector repaires injury caused by hypoxia/reoxygenation in cardiomyocyte cell line H9C2

YANG Jue-sheng1, FAN Hu-xiong3, HU Shan2, GAO Ri-feng3, LU Fei4, WANG Heng5, TANG Yan-hua1*   

  1. 1. Department of Cardiovascular Surgery;
    2. Department of Anesthesiology, the Second Affiliated Hospital of Nanchang University;
    3. Medical Department of Graduate School of Nanchang University;
    4. Department of Interventional , the Second Affiliated Hospital of Nanchang University, Nanchang 330031;
    5. Department of Cardiothoracic Surgery, Pingdingshan Second People's Hospital, Pingdingshan 467000, China
  • Received:2019-05-20 Revised:2019-06-26 Online:2020-02-05 Published:2020-02-05
  • Contact: *tyh8565@163.com

摘要: 目的 研究瞬时受体电位通道 7(TRPM7)干扰载体对低氧大鼠心肌细胞系(H9C2)修复功能的影响及其机理。方法 建立 H9C2心肌细胞低氧/复氧模型,构建 TRPM7 干扰表达载体转染H9C2细胞,用RT-qPCR与Western blot检测H9C2细胞低氧诱导因子(HIF1-α) 和 TRPM7 的表达,流式细胞计量术检测胞内钙离子水平([Ca2+]i)和细胞凋亡,确定 TRPM7 对H9C2心肌细胞的修复作用。结果 H9C2 细胞转染 TRPM7 干扰载体后,细胞的HIF1-α和TRPM7 表达显著下降(P<0.05),[Ca2+]i 降低及凋亡率减少(P<0.05)。结论 TRPM7 干扰载体可能通过 PI3K/Akt 通路对低氧 H9C2 心肌细胞有显著的修复作用。

关键词: TRPM7干扰载体, [Ca2+]i, 细胞凋亡

Abstract: Objective To study the repair function and mechanism of TRPM7 interference vector in hypoxic myocardial cell line (H9C2). Methods The hypoxia/reoxygenation model of H9C2 cardiomyocytes was established and the TRPM7 interference expression vector was constructed to transfect H9C2 cells. The expression of HIF1-α and TRPM7 in H9C2 cells was detected by RT-qPCR and Western blot. [Ca2+]i and apoptosis was determined by flow cytometry. Results When H9C2 cells were transfected with TRPM7 interference vector, the expression of HIF1-α TTRPM7, the [Ca2+]i concentration and the apoptosis rate all decreased. Conclusions TRPM7 interference vector has significant repairing effect on hypoxia H9C2 cardiomyocytes, and the mechanism may be mediated PI3K/Akt pathway.

Key words: TRPM7 interference vector, [Ca2+]i, cell apoptosis

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