Mironova Galina Yu, Haghbin Nadia, Welsh Donald G
Robarts Research Institute, Department of Physiology and Pharmacology Schulich School of Medicine, The University of Western Ontario, London, ON, Canada.
Front Physiol. 2022 Nov 15;13:1058744. doi: 10.3389/fphys.2022.1058744. eCollection 2022.
Vascular smooth muscle contraction is intimately tied to membrane potential and the rise in intracellular Ca enabled by the opening of L-type Ca channels. While voltage is often viewed as the single critical factor gating these channels, research is starting to reveal a more intricate scenario whereby their function is markedly tuned. This emerging concept will be the focus of this three-part review, the first part articulating the mechanistic foundation of contractile development in vascular smooth muscle. Part two will extend this foundational knowledge, introducing readers to functional coupling and how neighboring L-type Ca channels work cooperatively through signaling protein complexes, to facilitate their open probability. The final aspect of this review will discuss the impact of L-type Ca channel trafficking, a process tied to cytoskeleton dynamics. Cumulatively, this brief manuscript provides new insight into how voltage, along with channel cooperativity and number, work in concert to tune Ca responses and smooth muscle contraction.
血管平滑肌收缩与膜电位以及L型钙通道开放所引发的细胞内钙离子浓度升高密切相关。虽然电压常被视为这些通道开启的唯一关键因素,但研究开始揭示出一种更为复杂的情况,即它们的功能会受到显著调节。这一新兴概念将成为这篇分三部分的综述的焦点,第一部分阐述血管平滑肌收缩发育的机制基础。第二部分将扩展这一基础知识,向读者介绍功能偶联以及相邻的L型钙通道如何通过信号蛋白复合物协同工作,以提高其开放概率。本综述的最后一部分将讨论L型钙通道运输的影响,这一过程与细胞骨架动力学相关。总体而言,这篇简短的手稿为电压以及通道协同性和数量如何共同作用以调节钙离子反应和平滑肌收缩提供了新的见解。