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β 亚基在调控心肌细胞钠通道中的细胞黏附特性。

Cell-Adhesion Properties of β-Subunits in the Regulation of Cardiomyocyte Sodium Channels.

机构信息

Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, UK.

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.

出版信息

Biomolecules. 2020 Jul 1;10(7):989. doi: 10.3390/biom10070989.

Abstract

Voltage-gated sodium (Nav) channels drive the rising phase of the action potential, essential for electrical signalling in nerves and muscles. The Nav channel α-subunit contains the ion-selective pore. In the cardiomyocyte, Nav1.5 is the main Nav channel α-subunit isoform, with a smaller expression of neuronal Nav channels. Four distinct regulatory β-subunits (β1-4) bind to the Nav channel α-subunits. Previous work has emphasised the β-subunits as direct Nav channel gating modulators. However, there is now increasing appreciation of additional roles played by these subunits. In this review, we focus on β-subunits as homophilic and heterophilic cell-adhesion molecules and the implications for cardiomyocyte function. Based on recent cryogenic electron microscopy (cryo-EM) data, we suggest that the β-subunits interact with Nav1.5 in a different way from their binding to other Nav channel isoforms. We believe this feature may facilitate -cell-adhesion between β1-associated Nav1.5 subunits on the intercalated disc and promote ephaptic conduction between cardiomyocytes.

摘要

电压门控钠离子 (Nav) 通道驱动动作电位的上升相,这对于神经和肌肉中的电信号传导至关重要。Nav 通道 α 亚基包含离子选择性孔。在心肌细胞中,Nav1.5 是主要的 Nav 通道 α 亚基同工型,神经元 Nav 通道的表达较少。四个不同的调节 β 亚基(β1-4)与 Nav 通道 α 亚基结合。以前的工作强调了 β 亚基作为直接的 Nav 通道门控调节剂。然而,现在越来越认识到这些亚基还具有其他作用。在这篇综述中,我们专注于 β 亚基作为同亲性和异亲性细胞黏附分子,以及对心肌细胞功能的影响。基于最近的低温电子显微镜 (cryo-EM) 数据,我们提出 β 亚基与 Nav1.5 的相互作用方式与它们与其他 Nav 通道同工型的结合方式不同。我们认为这一特征可能促进连接蛋白上 Nav1.5 亚基之间的细胞黏附,并促进心肌细胞之间的电突触传导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14e8/7407995/e85d2a86c70a/biomolecules-10-00989-g001.jpg

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