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Persistence of Pro-Arrhythmic Spatio-Temporal Calcium Patterns in Atrial Myocytes: A Computational Study of Ping Waves

机译:心律失常时空钙模式在房性心肌细胞中的持久性:坪波的计算研究。

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摘要

Clusters of ryanodine receptors within atrial myocytes are confined to spatially separated layers. In many species, these layers are not juxtaposed by invaginations of the plasma membrane (transverse tubules; ‘T-tubules’), so that calcium-induced-calcium signals rely on centripetal propagation rather than voltage-synchronized channel openings to invade the interior of the cell and trigger contraction. The combination of this specific cellular geometry and dynamics of calcium release can lead to novel autonomous spatio-temporal calcium waves, and in particular ping waves. These are waves of calcium release activity that spread as counter-rotating sectors of elevated calcium within a single layer of ryanodine receptors, and can seed further longitudinal calcium waves. Here we show, using a computational model, that these calcium waves can dominate the response of a cell to electrical pacing and hence are pro-arrhythmic. This highlights the importance of modeling internal cellular structures when investigating mechanisms of cardiac dysfunction such as atrial arrhythmia.
机译:心房肌细胞内的瑞丹碱受体簇仅限于空间分隔的层。在许多物种中,这些层不与质膜的侵入并列(横向小管;“ T型小管”),因此钙诱导的钙信号依赖于向心传播,而不是电压同步的通道开口侵入内膜的内部。细胞并触发收缩。这种特定的细胞几何形状和钙释放动力学的结合可导致新的自主时空钙波,尤其是ping波。这些是钙释放活性的波,它们在单层的ryanodine受体内以升高的钙的反向旋转扇形传播,并且可以播种更多的纵向钙波。在这里,我们使用计算模型表明,这些钙波可以控制细胞对电起搏的反应,因此是促心律失常的。当研究心脏功能障碍(如心律失常)的机制时,这突出了对内部细胞结构建模的重要性。

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