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The mitochondrial calcium uniporter in the heart: energetics and beyond

机译:心脏中的线粒体钙钙蛋白:能量和超越

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摘要

Ca2+ and mitochondria are inextricably linked to cardiac function and dysfunction. Ca2+ is central to cardiac excitation-contraction coupling and stimulates mitochondrial energy production to fuel contraction. Under pathological conditions of dysregulated Ca2+ cycling, mitochondrial Ca2+ overload activates cellular death pathways. Thus, in the cardiomyocyte, the mitochondrial Ca2+ microdomain is where contraction, energy and death collide. A key component of mitochondrial Ca2+ signalling is the mitochondrial Ca2+ uniporter complex (uniplex), an inner membrane Ca2+ transporter and major pathway of mitochondrial Ca2+ entry. Once known only as the unidentified target for ruthenium red and related compounds, in recent years, the uniplex has evolved into a complex multiprotein assembly. The identification of the molecular constituents of the uniplex has made possible the generation of targeted genetic models to interrogate uniplex function in vivo. This review will summarize our current understanding of the molecular structure of the uniplex, its impact on mitochondrial energetics and cardiac physiology, its contribution to cardiomyocyte death, and its expanding roles in cardiac biology.
机译:Ca2 +和线粒体密不可分心脏功能和功能障碍。钙离子是中央心脏兴奋 - 收缩偶联并刺激线粒体能量产生燃料收缩。下失调的Ca2 +循环的病理条件下,线粒体的Ca 2+超载活化细胞死亡途径。因此,在心肌细胞,线粒体钙微区就是收缩,能量和死亡发生碰撞。线粒体钙信号传导的关键部件是线粒体的Ca 2+单向转运体复合物(单重),内细胞膜Ca2 +转运体和线粒体Ca 2+内流的主要途径。一旦人们只知道钌不明目标红色和相关化合物,在最近几年中,单重已演变成一个复杂的多蛋白组装。所述单重的分子组分的鉴定已经成为可能靶向遗传模型的产生来询问单路函数体内。这次审查将总结我们目前对线粒体能量学和心脏生理,其心肌细胞死亡的贡献,及其在心脏生物扩大作用的单路,其影响的分子结构的认识。

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