反应性氧物种诱导的心肌细胞亡中的信号通路
R von Harsdorf1, P F Li, R Dietz
1Department of Cardiology, Franz Volhard Clinic, Humboldt-University, Berlin, Germany. rharsdo@mdc-berlin.de
Circulation
|June 9, 1999
概括
反应性氧物种 (ROS) 通过不同的途径在心脏细胞中触发细胞亡. 过氧化激活了内在路径,而超氧化利用了涉及Mch2alpha的不同的路径,突出了ROS.
科学领域:
- 心血管生物学 心血管生物学
- 细胞信号传输 细胞信号传输
- 氧化压力研究研究 氧化压力研究
背景情况:
- 自由基平衡,亡和心脏健康之间的相互作用尚未得到充分理解.
- 研究活性氧物种 (ROS) 在心肌细胞亡中的作用对于理解心脏病至关重要.
研究的目的:
- 为了确定ROS是否可以在心肌细胞中诱导亡.
- 阐明涉及ROS介导心肌细胞亡的特定分子途径.
主要方法:
- 利用一个孤立的心脏细胞培养模型.
- 采用了各种ROS产生系统 (H2O2,超氧化离子).
- 分析了蛋白质表达 (p53,Bax,Bcl-2,Bad),蛋白质转位,以及酶激活 (CPP32,Mch2alpha).
主要成果:
- 无论是H2O2和超氧化离子都诱导了心肌细胞亡.
- H2O2诱导的亡包括p53,Bax,Bad转位,cytochrome c释放和CPP32激活.
- 超氧化离子诱导的亡利用Mch2alpha激活和层层A裂变,与H2O2路径不同.
结论:
- ROS在心脏病的病理生理学中发挥着重要作用,其中包括亡细胞死亡.
- 明显的ROS通过单独的信号级联触发心肌细胞亡,提供潜在的治疗点.
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