Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, UK.
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Biomolecules. 2020 Jul 1;10(7):989. doi: 10.3390/biom10070989.
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.
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。