线粒体通透性转换孔
心肌保护
效应器
化学
线粒体
细胞生物学
磁导率
生物物理学
缺血
生物
膜
医学
生物化学
心脏病学
程序性细胞死亡
细胞凋亡
作者
Paolo Bernardi,Fabio Di Lisa
标识
DOI:10.1016/j.yjmcc.2014.09.023
摘要
The mitochondrial permeability transition (PT) - an abrupt increase permeability of the inner membrane to solutes - is a causative event in ischemia-reperfusion injury of the heart, and the focus of intense research in cardioprotection. The PT is due to opening of the PT pore (PTP), a high conductance channel that is critically regulated by a variety of pathophysiological effectors. Very recent work indicates that the PTP forms from the F-ATP synthase, which would switch from an energy-conserving to an energy-dissipating device. This review provides an update on the current debate on how this transition is achieved, and on the PTP as a target for therapeutic intervention. This article is part of a Special Issue entitled "Mitochondria: from basic mitochondrial biology to cardiovascular disease".
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