基础医学与临床 ›› 2019, Vol. 39 ›› Issue (4): 536-540.

• 研究论文 • 上一篇    下一篇

Klotho蛋白减轻低氧/复氧诱导的心肌细胞系H9C2损伤

李宁,孙满意,孙国勇   

  1. 山东大学第二医院
  • 收稿日期:2018-08-28 修回日期:2018-12-25 出版日期:2019-04-05 发布日期:2019-03-26
  • 通讯作者: 孙国勇 E-mail:3076310840@qq.com
  • 基金资助:
    七氟醚吸入对发育期大鼠海马区神经元突触可塑性及生长相关蛋白43表达的影响的研究

Klotho protein attenuates hypoxia/reoxygenation-induced injury in myocardial cell line H9C2

  • Received:2018-08-28 Revised:2018-12-25 Online:2019-04-05 Published:2019-03-26

摘要: 目的 研究klotho蛋白对低氧-复氧诱导的心肌H9C2细胞系损伤的保护作用及其机制。方法 将H9C2心肌细胞分为对照组、低氧/复氧组(1% O2低氧6 h, 5% CO2以及95%空气培养箱中复氧2 h)和klotho蛋白(10 μg/mL)干预组。通过酶标仪间接测定细胞内钙离子([Ca2+]i)水平;CCK8法和TUNEL法分别检测细胞活性及细胞凋亡;分光光度法检测细胞中钠ATP酶(Na+/ K+ - ATPase,NKA)和反向模式钠/钙交换体(Na+/Ca2+-exchange,NCX)的活性。结果 体外培养的H9C2细胞低氧/复氧(6 h/2 h)处理后可明显降低H9C2细胞活性(p<0.05);增加细胞内Ca2+水平和凋亡率(p<0.05);降低细胞中Na+/ K+ - ATPase的活性(p<0.05);增加反向模式Na+/Ca2+交换体的活性(p<0.05);10 μg/mL klotho蛋白处理可明显减轻上述损伤。结论 klotho蛋白可减轻低氧/复氧诱导下的H9C2细胞内钙超载,最终减少该细胞株细胞的凋亡。

关键词: klotho蛋白, H9C2细胞, 心肌保护 , 钠钾ATP酶, 钠钙交换体

Abstract: Objective To investigate the protective effect and mechanism of klotho protein on hypoxia/reoxygenation-induced injury in H9C2 cells line. Methods H9C2 cells were cultured and divided into control group, hypoxia/reoxygenation group (cells were treated with 1% O2 for 6 h hypoxia and then reoxygenation in 5% CO2 and 95% air for 2 h) and klotho protein intervention group (10 μg/ml). Intracellular calcium level was determined indirectly by microplate reader; CCK8 and TUNEL assay was used to detect the cell viability and cell apoptosis respectively. Spectrophotometry was used to evaluate the activity of Na+/ K+ - ATPase (NKA) and the reverse mode of Na+/Ca2+-exchange (NCX). Results Hypoxia/reoxygenation (6h/2h) treatment of H9C2 cells in vitro could significantly reduce its cell viability (p <0.01), increase intracellular Ca2+ ([Ca2+]i) and apoptosis rate (p<0.01). Moreover, the activity of Na+/ K+ - ATPase (NKA) was decreased and the the activity of reverse mode of Na+/Ca2+-exchange (NCX) was increased in cultured H9C2 cells treating with hypoxia/reoxygenation. However, the klotho protein administration observably attenuated all these changes (p<0.01). Conclusions klotho protein administration can attenuate hypoxia/reoxygenation induced intracellular calcium overload and high apoptosis rate in cultured H9C2 cells.

Key words: klotho protein, H9C2 cells, myocardial protection, Na+/K+-ATPase, Na+/Ca2+-exchanger