Yang Shao-Nian, Berggren Per-Olof
The Rolf Luft Center for Diabetes Research, Karolinska Diabetes Center, Department of Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Am J Physiol Endocrinol Metab. 2005 Jan;288(1):E16-28. doi: 10.1152/ajpendo.00042.2004.
The beta-cell is equipped with at least six voltage-gated Ca2+ (CaV) channel alpha1-subunits designated CaV1.2, CaV1.3, CaV2.1, CaV2.2, CaV2.3, and CaV3.1. These principal subunits, together with certain auxiliary subunits, assemble into different types of CaV channels conducting L-, P/Q-, N-, R-, and T-type Ca2+ currents, respectively. The beta-cell shares customary mechanisms of CaV channel regulation with other excitable cells, such as protein phosphorylation, Ca2+-dependent inactivation, and G protein modulation. However, the beta-cell displays some characteristic features to bring these mechanisms into play. In islet beta-cells, CaV channels can be highly phosphorylated under basal conditions and thus marginally respond to further phosphorylation. In beta-cell lines, CaV channels can be surrounded by tonically activated protein phosphatases dominating over protein kinases; thus their activity is dramatically enhanced by inhibition of protein phosphatases. During the last 10 years, we have revealed some novel mechanisms of beta-cell CaV channel regulation under physiological and pathophysiological conditions, including the involvement of exocytotic proteins, inositol hexakisphosphate, and type 1 diabetic serum. This minireview highlights characteristic features of customary mechanisms of CaV channel regulation in beta-cells and also reviews our studies on newly identified mechanisms of beta-cell CaV channel regulation.
β细胞至少配备有六种电压门控Ca2+(CaV)通道α1亚基,分别命名为CaV1.2、CaV1.3、CaV2.1、CaV2.2、CaV2.3和CaV3.1。这些主要亚基与某些辅助亚基一起,组装成不同类型的CaV通道,分别传导L型、P/Q型、N型、R型和T型Ca2+电流。β细胞与其他可兴奋细胞具有共同的CaV通道调节机制,如蛋白质磷酸化、Ca2+依赖性失活和G蛋白调节。然而,β细胞表现出一些特征性特点来发挥这些机制的作用。在胰岛β细胞中,CaV通道在基础条件下可被高度磷酸化,因此对进一步的磷酸化反应微弱。在β细胞系中,CaV通道可被持续激活的蛋白磷酸酶所包围,其作用强于蛋白激酶;因此,抑制蛋白磷酸酶可显著增强其活性。在过去10年中,我们揭示了生理和病理生理条件下β细胞CaV通道调节的一些新机制,包括胞吐蛋白、肌醇六磷酸和1型糖尿病血清的参与。这篇小型综述重点介绍了β细胞中CaV通道调节常见机制的特征,并回顾了我们对新发现的β细胞CaV通道调节机制的研究。