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Microdomain–specific localization of functional ion channels in cardiomyocytes: an emerging concept of local regulation and remodelling

机译:心肌细胞中功能性离子通道的微区特异性定位:局部调节和重塑的新兴概念

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摘要

Cardiac excitation involves the generation of action potential by individual cells and the subsequent conduction of the action potential from cell to cell through intercellular gap junctions. Excitation of the cellular membrane results in opening of the voltage-gated L-type calcium ion (Ca2+) channels, thereby allowing a small amount of Ca2+ to enter the cell, which in turn triggers the release of a much greater amount of Ca2+ from the sarcoplasmic reticulum, the intracellular Ca2+ store, and gives rise to the systolic Ca2+ transient and contraction. These processes are highly regulated by the autonomic nervous system, which ensures the acute and reliable contractile function of the heart and the short-term modulation of this function upon changes in heart rate or workload. It has recently become evident that discrete clusters of different ion channels and regulatory receptors are present in the sarcolemma, where they form an interacting network and work together as a part of a macro-molecular signalling complex which in turn allows the specificity, reliability and accuracy of the autonomic modulation of the excitation–contraction processes by a variety of neurohormonal pathways. Disruption in subcellular targeting of ion channels and associated signalling proteins may contribute to the pathophysiology of a variety of cardiac diseases, including heart failure and certain arrhythmias. Recent methodological advances have made it possible to routinely image the topography of live cardiomyocytes, allowing the study of clustering functional ion channels and receptors as well as their coupling within a specific microdomain. In this review we highlight the emerging understanding of the functionality of distinct subcellular microdomains in cardiac myocytes (e.g. T-tubules, lipid rafts/caveolae, costameres and intercalated discs) and their functional role in the accumulation and regulation of different subcellular populations of sodium, Ca2+ and potassium ion channels and their contributions to cellular signalling and cardiac pathology.
机译:心脏兴奋涉及单个细胞产生动作电位,以及随后动作电位通过细胞间间隙连接在细胞之间传导。激发细胞膜会导致电压门控L型钙离子(Ca 2 + )通道打开,从而使少量Ca 2 + 进入细胞,进而触发肌浆网,细胞内Ca 2 + 存储区释放出大量的Ca 2 + ,并引起收缩压Ca 2 + 瞬变和收缩。这些过程受到植物神经系统的高度调节,从而确保了心脏的急性和可靠收缩功能,并在心率或工作量发生变化时对其进行短期调节。最近发现,在肌膜中存在不同离子通道和调节受体的离散簇,它们形成相互作用的网络并作为大分子信号复合体的一部分协同工作,从而又可以实现特异性,可靠性和准确性各种神经激素途径对兴奋-收缩过程的自主调节作用离子通道和相关信号蛋白在亚细胞靶向中的破坏可能有助于多种心脏疾病的病理生理,包括心脏衰竭和某些心律不齐。最近的方法学进展使得常规地对活心肌细胞的地形成像成为可能,从而允许研究功能性离子通道和受体的聚集以及它们在特定微域内的偶联。在这篇综述中,我们重点介绍了对心肌细胞中不同亚细胞微结构域(例如T管,脂质筏/小窝,肋骨和插入椎间盘)的功能的认识,以及它们在不同亚细胞钠的积累和调节中的功能作用, Ca 2 + 和钾离子通道及其对细胞信号传导和心脏病理的贡献。

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