Kurachi Y
Department of Pharmacology II, Faculty of Medicine, Osaka University, Japan.
Am J Physiol. 1995 Oct;269(4 Pt 1):C821-30. doi: 10.1152/ajpcell.1995.269.4.C821.
Several ion channels can be regulated by G proteins in a "membrane-delimited" manner. The cardiac muscarinic K+ (KACh) channel, which is responsible for the acetylcholine (ACh) or adenosine-induced deceleration of heart beat and atrioventricular conduction, is the prototype of this type of receptor-dependent regulation of ion channels. Because similar transduction mechanisms are utilized by various membrane receptors, such as somatostatin, 5-hydroxytryptamine-1, alpha 2-adrenergic, mu-and delta-opioid, D2-dopamine, and gamma-aminobutyric acid B receptors, in neuronal, hormone-secreting, renal, or smooth muscle cells, the G protein (GK)-KACh channel system illustrates the principles underlying one of the most important cell signaling mechanisms (B. Hille. Neuron 9: 187-195, 1992). It seems that both alpha- and beta gamma-subunits of GK may be involved in the regulation of the KACh channel of mammalian atrial muscle. A general consensus of opinion has emerged, after some years of controversy, to support the notion that physiological activation of the channel by GK is the responsibility of the beta gamma-subunits. Recent evidence suggests that the KACh channel interacts with the alpha-subunit in the terminating process of activation.
几种离子通道可被G蛋白以“膜限定”方式调节。心脏毒蕈碱K⁺(KACh)通道负责乙酰胆碱(ACh)或腺苷诱导的心跳和房室传导减慢,是这种受体依赖性离子通道调节类型的原型。由于各种膜受体,如生长抑素、5-羟色胺-1、α₂-肾上腺素能、μ-和δ-阿片样物质、D₂-多巴胺和γ-氨基丁酸B受体,在神经元、激素分泌、肾或平滑肌细胞中利用相似的转导机制,G蛋白(GK)-KACh通道系统阐明了最重要的细胞信号传导机制之一的潜在原理(B. 希勒。《神经元》9:187 - 195,1992)。哺乳动物心房肌的KACh通道调节似乎可能涉及GK的α亚基和βγ亚基。经过数年的争论,已形成普遍共识,支持GK对通道的生理性激活由βγ亚基负责这一观点。最近的证据表明,KACh通道在激活终止过程中与α亚基相互作用。