Kwan C Y
Smooth Muscle Research Program, McMaster University Health Sciences Centre, Hamilton, Ont., Canada.
Can J Physiol Pharmacol. 1992 Apr;70(4):501-8. doi: 10.1139/y92-065.
Many of the contractile regulatory events in smooth muscle reside in various cellular membrane components as functional membrane constituents that interact in a variably complex manner. The physiological handling of ionized calcium (Ca2+), which serves multiple roles as an extracellular signal, a second messenger, and an activator interacting directly with myofilaments to effectuate contractile responses, referred to as Ca2+ signalling processes, represents an integral part of a more complicated membrane transduction mechanism. The subcellular membrane approach toward the understanding of Ca2+ signalling as well as the transduction mechanisms involving membrane receptors, GTP binding proteins, ion channels, membrane-bound enzymes, and the production of intracellular second messengers has made a significant contribution in smooth muscle research for the past decade. This review summarizes the current state of knowledge about the multiplicity of interactions between Ca2+ and various membrane constituents in the surface membranes and sarcoplasmic reticulum, such as Ca2+ binding, Ca2+ ATPase pumps, Ca2+ channels, and Ca2+Na+ or related ion exchangers. A number of recent novel findings from this laboratory have also been discussed. First of all, the technical refinement of membrane separation and characterization, which permits better identification of neuronal membranes in highly innervated smooth muscle tissues, led to the distinction of prejunctional and postjunctional membrane receptors. Secondly, unlike the Ca(2+)-release channels labelled with [3H]inositol 1,4,5-trisphosphate, the other type of internal membrane Ca(2+)-release channels labelled by [3H]ryanodine has been identified only recently in smooth muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
平滑肌中的许多收缩调节事件存在于各种细胞膜成分中,这些成分作为功能性膜成分,以复杂多变的方式相互作用。离子钙(Ca2+)的生理调控具有多种作用,它既是细胞外信号、第二信使,又是直接与肌丝相互作用以引发收缩反应的激活剂,即Ca2+信号传导过程,是更复杂的膜转导机制的一个组成部分。在过去十年中,通过亚细胞膜方法来理解Ca2+信号传导以及涉及膜受体、GTP结合蛋白、离子通道、膜结合酶和细胞内第二信使产生的转导机制,在平滑肌研究中做出了重大贡献。本综述总结了目前关于Ca2+与表面膜和肌浆网中各种膜成分之间多种相互作用的知识状态,如Ca2+结合、Ca2+ATP酶泵、Ca2+通道以及Ca2+ - Na+或相关离子交换体。本文还讨论了本实验室最近的一些新发现。首先,膜分离和表征技术的改进使得在高度神经支配的平滑肌组织中能更好地识别神经元膜,从而区分了接头前和接头后膜受体。其次,与用[3H]肌醇1,4,5 - 三磷酸标记的Ca(2+)释放通道不同,另一种用[3H]ryanodine标记的内膜Ca(2+)释放通道直到最近才在平滑肌中被鉴定出来。(摘要截短于250字)