Department of Neuroscience, NIS Centre, Università di Torino, Turin, Italy.
Channels (Austin). 2010 Nov-Dec;4(6):440-6. doi: 10.4161/chan.4.6.12866. Epub 2010 Nov 1.
Voltage-gated L-type calcium channels (LTCCs) are expressed in adrenal chromaffin cells. Besides shaping the action potential (AP), LTCCs are involved in the excitation-secretion coupling controlling catecholamine release and in Ca (2+) -dependent vesicle retrieval. Of the two LTCCs expressed in chromaffin cells (CaV1.2 and CaV1.3), CaV1.3 possesses the prerequisites for pacemaking spontaneously firing cells: low-threshold, steep voltage-dependence of activation and slow inactivation. By using CaV1 .3 (-/-) KO mice and the AP-clamp it has been possible to resolve the time course of CaV1.3 pacemaker currents, which is similar to that regulating substantia nigra dopaminergic neurons. In mouse chromaffin cells CaV1.3 is coupled to fast-inactivating BK channels within membrane nanodomains and controls AP repolarization. The ability to carry subthreshold Ca (2+) currents and activate BK channels confers to CaV1.3 the unique feature of driving Ca (2+) loading during long interspike intervals and, possibly, to control the Ca (2+) -dependent exocytosis and endocytosis processes that regulate catecholamine secretion and vesicle recycling.
电压门控 L 型钙通道(LTCCs)在肾上腺嗜铬细胞中表达。除了塑造动作电位(AP)外,LTCCs 还参与兴奋-分泌偶联,控制儿茶酚胺的释放,并参与 Ca(2+)依赖性囊泡回收。在嗜铬细胞中表达的两种 LTCCs(CaV1.2 和 CaV1.3)中,CaV1.3 具有自发发射细胞起搏的先决条件:低阈值、激活的陡峭电压依赖性和缓慢失活。通过使用 CaV1.3(-/-)KO 小鼠和 AP 钳,已经可以解析 CaV1.3 起搏电流的时间过程,其类似于调节黑质多巴胺能神经元的时间过程。在小鼠嗜铬细胞中,CaV1.3 与膜纳米域内快速失活的 BK 通道偶联,并控制 AP 复极化。携带亚阈值 Ca(2+)电流和激活 BK 通道的能力赋予 CaV1.3 独特的功能,即在长的峰间间隔期间驱动 Ca(2+)加载,并可能控制调节儿茶酚胺分泌和囊泡回收的 Ca(2+)依赖性胞吐和胞吞过程。