钙
线粒体
Uniporter公司
细胞生物学
线粒体基质
生物
钙信号传导
钙代谢
胞浆
生物化学
化学
信号转导
酶
有机化学
作者
Toren Finkel,Sara Menazza,Kira M. Holmström,Randi J. Parks,Julia Liu,Junhui Sun,Jie Liu,Xin Pan,Elizabeth Murphy
出处
期刊:Circulation Research
[Ovid Technologies (Wolters Kluwer)]
日期:2015-05-22
卷期号:116 (11): 1810-1819
被引量:194
标识
DOI:10.1161/circresaha.116.305484
摘要
Calcium is thought to play an important role in regulating mitochondrial function. Evidence suggests that an increase in mitochondrial calcium can augment ATP production by altering the activity of calcium-sensitive mitochondrial matrix enzymes. In contrast, the entry of large amounts of mitochondrial calcium in the setting of ischemia-reperfusion injury is thought to be a critical event in triggering cellular necrosis. For many decades, the details of how calcium entered the mitochondria remained a biological mystery. In the past few years, significant progress has been made in identifying the molecular components of the mitochondrial calcium uniporter complex. Here, we review how calcium enters and leaves the mitochondria, the growing insight into the topology, stoichiometry and function of the uniporter complex, and the early lessons learned from some initial mouse models that genetically perturb mitochondrial calcium homeostasis.
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