Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, New York, NY, USA.
J Mol Cell Cardiol. 2012 Feb;52(2):304-11. doi: 10.1016/j.yjmcc.2011.06.024. Epub 2011 Jul 13.
Evidence obtained in recent years indicates that, in cardiac myocytes, release of Ca(2+) from the sarcoplasmic reticulum (SR) is regulated by changes in the concentration of Ca(2+) within the SR. In this review, we summarize recent advances in our understanding of this regulatory role, with a particular emphasis on dynamic and local changes in SR [Ca(2+)]. We focus on five important questions that are to some extent unresolved and controversial. These questions concern: (1) the importance of SR [Ca(2+)] depletion in the termination of Ca(2+) release; (2) the quantitative extent of depletion during local release events such as Ca(2+) sparks; (3) the influence of SR [Ca(2+)] refilling on release refractoriness and the propensity for pathological Ca(2+) release; (4) dynamic changes in SR [Ca(2+)] during propagating Ca(2+) waves; and (5) the speed of Ca(2+) diffusion within the SR. With each issue, we discuss data supporting alternative viewpoints, and we identify fundamental questions that are being actively investigated. We conclude with a discussion of experimental and computational advances that will help to resolve controversies. This article is part of a special issue entitled "Local Signaling in Myocytes."
近年来的证据表明,在心肌细胞中,肌浆网 (SR) 中 Ca(2+) 的释放受 SR 内 Ca(2+) 浓度变化的调节。在这篇综述中,我们总结了对这种调节作用的最新理解进展,特别强调了 SR [Ca(2+)] 的动态和局部变化。我们重点关注了五个在某种程度上尚未解决且存在争议的重要问题。这些问题涉及:(1) SR [Ca(2+)] 耗竭在终止 Ca(2+) 释放中的重要性;(2) 局部释放事件(如 Ca(2+) 火花)期间的耗竭程度;(3) SR [Ca(2+)] 再填充对释放不应期和病理性 Ca(2+) 释放倾向的影响;(4) 传播 Ca(2+) 波期间 SR [Ca(2+)] 的动态变化;以及 (5) SR 内 Ca(2+) 的扩散速度。对于每个问题,我们讨论了支持替代观点的数据,并确定了正在积极研究的基本问题。最后,我们讨论了有助于解决争议的实验和计算进展。本文是题为“心肌细胞中的局部信号转导”的特刊的一部分。