Pochynyuk Oleh, Stockand James D, Staruschenko Alexander
Department of Physiology, University of Texas Health Science Center, San Antonio, Texas 78229-3900, USA.
Exp Biol Med (Maywood). 2007 Nov;232(10):1258-65. doi: 10.3181/0703-MR-76.
Regulation of ion channels by heterotrimeric guanosine triphosphatases (GTPases), activated by heptathelical membrane receptors, has been the focus of several recent reviews. In comparison, regulation of ion channels by small monomeric G proteins, activated by cytoplasmic guanine nucleotide exchange factors, has been less well reviewed. Small G proteins, molecular switches that control the activity of cellular and membrane proteins, regulate a wide variety of cell functions. Many upstream regulators and downstream effectors of small G proteins now have been isolated. Their modes of activation and action are understood. Recently, ion channels were recognized as physiologically important effectors of small GTPases. Recent advances in understanding how small G proteins regulate the intracellular trafficking and activity of ion channels are discussed here. We aim to provide critical insight into physiological control of ion channel function and the biological consequences of regulation of these important proteins by small, monomeric G proteins.
由七螺旋膜受体激活的异源三聚体鸟苷三磷酸酶(GTPases)对离子通道的调节,一直是近期几篇综述的焦点。相比之下,由细胞质鸟嘌呤核苷酸交换因子激活的小单体G蛋白对离子通道的调节,受到的综述较少。小G蛋白作为控制细胞和膜蛋白活性的分子开关,调节着多种细胞功能。现在已经分离出许多小G蛋白的上游调节因子和下游效应器。它们的激活方式和作用机制也已为人所知。最近,离子通道被认为是小GTPases在生理上的重要效应器。本文将讨论在理解小G蛋白如何调节离子通道的细胞内运输和活性方面的最新进展。我们旨在深入洞察离子通道功能的生理控制,以及小单体G蛋白对这些重要蛋白质的调节所产生的生物学后果。