O'Rourke Brian, Cortassa Sonia, Aon Miguel A
Institute of Molecular Cardiobiology, Division of Cardiology, The Johns Hopkins University, Baltimore, Maryland, USA.
Physiology (Bethesda). 2005 Oct;20:303-15. doi: 10.1152/physiol.00020.2005.
Continuous generation of ATP by mitochondrial oxidative phosphorylation is essential to maintain function in mechanically active cells such as cardiomyocytes. Emerging evidence indicates that mitochondrial ion channels activated by reactive oxygen species can induce a mitochondrial "critical" state, which can scale to cause electrical and contractile dysfunction of the cardiac cell and, ultimately, the whole heart. Here we focus on how mitochondrial ion channels participate in life-and-death decisions of the cell and discuss the challenges ahead for translating recent findings into novel therapeutic applications.
线粒体氧化磷酸化持续产生三磷酸腺苷(ATP)对于维持诸如心肌细胞等机械活性细胞的功能至关重要。新出现的证据表明,由活性氧激活的线粒体离子通道可诱导线粒体“临界”状态,这种状态可能会扩展,导致心脏细胞以及最终整个心脏的电功能和收缩功能障碍。在这里,我们重点关注线粒体离子通道如何参与细胞的生死抉择,并讨论将近期研究结果转化为新型治疗应用面临的挑战。