betway必威登陆网址 (betway.com )学报››2023,Vol. 44››Issue (4): 273-277.DOI:10.3969/j.issn.2097-0005.2023.04.007

• 基础研究 •上一篇下一篇

HIF-1α通过激活Notch通路缓解活性氧诱导的心肌细胞凋亡

冯桂菊(), 张红, 王守燕, 郭依, 沈鑫, 钟霞()

  1. betway必威登陆网址 附属省立医院全科医学科,山东 济南 250021
  • 收稿日期:2022-11-19出版日期:2023-04-25发布日期:2023-05-15
  • 通讯作者:钟霞
  • 作者简介:冯桂菊,硕士研究生,研究方向:心血管内科,E-mail:fengguiju2020413@163.com
  • 基金资助:
    山东省自然科学基金(ZR2020MH036);济南市科技创新计划(202019078)

HIF-1α in protecting cardiomyocytes from reactive oxygen species-induced cardiomyocyte apoptosis by activating the Notch pathway

Guiju FENG(), Hong ZHANG, Shouyan WANG, Yi GUO, Xin SHEN, Xia ZHONG()

  1. Department of General Practice,Shandong Provincial Hospital Affiliated to Shandong First Medical University,Jinan 250021,China.
  • Received:2022-11-19Online:2023-04-25Published:2023-05-15
  • Contact:Xia ZHONG

摘要:

目的探讨缺氧诱导因子-1α(hypoxia inducible factor-1α, HIF-1α)在心肌细胞氧化损伤中的作用及其机制。方法应用过氧化氢(H2O2)构建体外心肌细胞氧化损伤模型,采用实时荧光定量聚合酶链反应(qRT-PCR)检测HIF-1α及通路相关基因如Notch胞内结构域(notch intracellular domain, NICD)、Hes-1的表达;分别采用细胞计数试剂盒-8(CCK-8)和流式细胞术检测细胞活力和细胞凋亡;采用蛋白印迹法测定蛋白水平。结果在经H2O2处理的人AC16心肌细胞中,HIF-1α表达上调;过氧化氢处理可抑制细胞活力并促进细胞凋亡;敲除HIF-1α抑制了Notch信号通路中关键成分的表达,加重了H2O2诱导的心肌细胞凋亡。结论HIF-1α可通过激活Notch通路减轻活性氧诱导的心肌细胞凋亡。

关键词:缺氧诱导因子-1α,缺血再灌注损伤,活性氧,Notch信号通路,凋亡

Abstract:

ObjectiveTo investigate the role and mechanism of HIF-1α in cardiac myocyte oxidative injury.MethodsThe classic oxidative injury model of cardiomyocytes with H2O2was established. The expression of HIF-1α and pathway-related genes were tested by quantitative real-time polymerase chain reaction. Cell viability and apoptosis were detected by cell counting kit-8 and flow cytometry analysis respectively. The protein levels were estimated by western blot.ResultsHIF-1α was expressed at a high level in human AC16 cardiomyocytes treated with hydrogen peroxide or hypoxia/reoxygenation. Knock down of HIF-1α restrained the Notch signaling pathway and aggravated H2O2-induced cardiomyocyte apoptosis.ConclusionHIF-1α protects cardiomyocytes from reactive oxygen species-induced apoptosis by regulating the Notch pathway.

Key words:hypoxia-inducible factor 1α,ischemia-reperfusion injury,reactive oxygen species,Notch pathway,apoptosis