郭伟楠, 殷 玥, 综述, 马 恒, 审校. 缺血/再灌注后心肌细胞死亡方式的选择及其机制探讨[J]. 心脏杂志, 2015, 27(4): 470-473.
    引用本文: 郭伟楠, 殷 玥, 综述, 马 恒, 审校. 缺血/再灌注后心肌细胞死亡方式的选择及其机制探讨[J]. 心脏杂志, 2015, 27(4): 470-473.
    Indicators and mechanism of myocardial cell death after ischemia/reperfusion[J]. Chinese Heart Journal, 2015, 27(4): 470-473.
    Citation: Indicators and mechanism of myocardial cell death after ischemia/reperfusion[J]. Chinese Heart Journal, 2015, 27(4): 470-473.

    缺血/再灌注后心肌细胞死亡方式的选择及其机制探讨

    Indicators and mechanism of myocardial cell death after ischemia/reperfusion

    • 摘要: 心肌缺血/再灌注(MI/R)损伤是临床治疗中亟待解决的问题。心肌细胞为终末细胞,MI/R损伤导致的心肌细胞死亡会不可逆地损伤心脏的结构和功能,导致心肌纤维化、心衰等后果。坏死和凋亡是心肌细胞死亡的两种主要方式。以往认为,坏死是非程序性的细胞死亡。近期研究发现,心肌细胞的坏死并非不可控,坏死也受细胞内信号机制调控,称为程序性坏死(necroptosis)。MI/R后,通过心肌细胞膜上的死亡受体介导,心肌细胞可以经一系列可调节的分子信号通路,在凋亡和程序性坏死中做出选择。本文就MI/R后心肌细胞死亡方式的选择及其调控机制作一综述。

       

      Abstract: Myocardial ischemia/reperfusion (MI/R) injury is a problem urgently needed to be solved in clinical treatment. Myocardial cells are end cells. The death of myocardial cells caused by MI/R injury can lead to irreversible damage of the heart structure and functions and result in myocardial fibrosis and heart failure. Necrosis and apoptosis are the two main indicators of myocardial cell death. Necrosis was regarded as non-programmed cell death. However, recent studies revealed that myocyte necrosis is not uncontrollable and can be regulated by signaling pathways, referred to as necroptosis. After MI/R, myocardial cells, with the mediation of the death receptors on myocardial cell membranes, may make a choice between apoptosis and necroptosis through a series of regulated molecular signaling pathways. In this review,indicators of myocardial cell death after ischemia/reperfusion and its mechanisms are discussed.

       

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