Vandael D H F, Mahapatra S, Calorio C, Marcantoni A, Carbone E
Department of Drug Science, Laboratory of Cellular & Molecular Neuroscience, NIS Center, CNISM, University of Torino, Italy.
Biochim Biophys Acta. 2013 Jul;1828(7):1608-18. doi: 10.1016/j.bbamem.2012.11.013. Epub 2012 Nov 15.
Voltage-gated Ca²⁺ channels (VGCCs) are voltage sensors that convert membrane depolarizations into Ca²⁺ signals. In the chromaffin cells of the adrenal medulla, the Ca²⁺ signals driven by VGCCs regulate catecholamine secretion, vesicle retrievals, action potential shape and firing frequency. Among the VGCC-types expressed in these cells (N-, L-, P/Q-, R- and T-types), the two L-type isoforms, Ca(v)1.2 and Ca(v)1.3, control key activities due to their particular activation-inactivation gating and high-density of expression in rodents and humans. The two isoforms are also effectively modulated by G protein-coupled receptor pathways delimited in membrane micro-domains and by the cAMP/PKA and NO/cGMP/PKG phosphorylation pathways which induce prominent Ca²⁺ current changes if opposingly regulated. The two L-type isoforms shape the action potential and directly participate to vesicle exocytosis and endocytosis. The low-threshold of activation and slow rate of inactivation of Ca(v)1.3 confer to this channel the unique property of carrying sufficient inward current at subthreshold potentials able to activate BK and SK channels which set the resting potential, the action potential shape, the cell firing mode and the degree of spike frequency adaptation during spontaneous firing or sustained depolarizations. These properties help chromaffin cells to optimally adapt when switching from normal to stress-mimicking conditions. Here, we will review past and recent findings on cAMP- and cGMP-mediated modulations of Ca(v)1.2 and Ca(v)1.3 and the role that these channels play in the control of chromaffin cell firing. This article is part of a Special Issue entitled: Calcium channels.
电压门控Ca²⁺通道(VGCCs)是将膜去极化转化为Ca²⁺信号的电压传感器。在肾上腺髓质的嗜铬细胞中,由VGCCs驱动的Ca²⁺信号调节儿茶酚胺分泌、囊泡回收、动作电位形状和发放频率。在这些细胞中表达的VGCC类型(N型、L型、P/Q型、R型和T型)中,两种L型亚型Ca(v)1.2和Ca(v)1.3因其特殊的激活-失活门控以及在啮齿动物和人类中的高密度表达而控制着关键活动。这两种亚型还受到膜微区中限定的G蛋白偶联受体途径以及cAMP/PKA和NO/cGMP/PKG磷酸化途径的有效调节,如果这些途径受到相反调节,则会引起显著的Ca²⁺电流变化。这两种L型亚型塑造动作电位,并直接参与囊泡的胞吐作用和内吞作用。Ca(v)1.3的低激活阈值和缓慢的失活速率赋予该通道独特的特性,即在阈下电位携带足够的内向电流,能够激活设定静息电位、动作电位形状、细胞发放模式以及自发发放或持续去极化期间的动作电位频率适应程度的BK和SK通道。这些特性有助于嗜铬细胞在从正常状态转变为模拟应激状态时进行最佳适应。在此,我们将回顾过去和最近关于cAMP和cGMP介导的对Ca(v)1.2和Ca(v)1.3的调节以及这些通道在控制嗜铬细胞发放中所起作用的研究发现。本文是名为“钙通道”的特刊的一部分。