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RyR2 不应期缩短决定了心律失常基因模型中心肌异常钙释放的同步性。

Decreased RyR2 refractoriness determines myocardial synchronization of aberrant Ca2+ release in a genetic model of arrhythmia.

机构信息

D. Davis Heart and Lung Research Institute, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10312-7. doi: 10.1073/pnas.1300052110. Epub 2013 Jun 3.

Abstract

Dysregulated intracellular Ca(2+) signaling is implicated in a variety of cardiac arrhythmias, including catecholaminergic polymorphic ventricular tachycardia. Spontaneous diastolic Ca(2+) release (DCR) can induce arrhythmogenic plasma membrane depolarizations, although the mechanism responsible for DCR synchronization among adjacent myocytes required for ectopic activity remains unclear. We investigated the synchronization mechanism(s) of DCR underlying untimely action potentials and diastolic contractions (DCs) in a catecholaminergic polymorphic ventricular tachycardia mouse model with a mutation in cardiac calsequestrin. We used a combination of different approaches including single ryanodine receptor channel recording, optical imaging (Ca(2+) and membrane potential), and contractile force measurements in ventricular myocytes and intact cardiac muscles. We demonstrate that DCR occurs in a temporally and spatially uniform manner in both myocytes and intact myocardial tissue isolated from cardiac calsequestrin mutation mice. Such synchronized DCR events give rise to triggered electrical activity that results in synchronous DCs in the myocardium. Importantly, we establish that synchronization of DCR is a result of a combination of abbreviated ryanodine receptor channel refractoriness and the preceding synchronous stimulated Ca(2+) release/reuptake dynamics. Our study reveals how aberrant DCR events can become synchronized in the intact myocardium, leading to triggered activity and the resultant DCs in the settings of a cardiac rhythm disorder.

摘要

细胞内钙离子信号失调与多种心律失常有关,包括儿茶酚胺多形性室性心动过速。自发性舒张期 Ca(2+)释放(DCR)可引起致心律失常的细胞膜去极化,尽管导致异位活动的相邻心肌细胞中 DCR 同步的机制尚不清楚。我们研究了心脏 calsequestrin 突变的儿茶酚胺多形性室性心动过速小鼠模型中,DCR 下不及时动作电位和舒张收缩(DC)的同步机制。我们使用了包括单个ryanodine 受体通道记录、光学成像(Ca(2+)和膜电位)和心室肌细胞和完整心肌组织的收缩力测量在内的不同方法的组合。我们证明 DCR 在心脏 calsequestrin 突变小鼠的心肌细胞和完整心肌组织中以时间和空间均匀的方式发生。这种同步的 DCR 事件产生触发电活动,导致心肌中的同步 DC。重要的是,我们确定 DCR 的同步是缩短ryanodine 受体通道不应期和先前同步刺激 Ca(2+)释放/摄取动力学的组合的结果。我们的研究揭示了异常的 DCR 事件如何在完整的心肌中同步,导致在心脏节律紊乱的情况下触发活动和随后的 DC。

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