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平滑肌收缩的机制。

Mechanisms of smooth muscle contraction.

作者信息

Horowitz A, Menice C B, Laporte R, Morgan K G

机构信息

Boston Biomedical Research Institute, Boston, Massachusetts, USA.

出版信息

Physiol Rev. 1996 Oct;76(4):967-1003. doi: 10.1152/physrev.1996.76.4.967.

Abstract

Work performed with differentiated contractile smooth muscle tissue over the last two decades has made clear that covalent modification of myosin by phosphorylation of the 20-kDa myosin light chains is a significant mode of regulation of contractile activity in smooth muscle, particularly in regard to the generation of phasic contractions and the initial development of tonic contractions. This regulatory mechanism appears to be of unique importance in smooth muscle compared with striated muscle. It is equally clear, however, that there is an important role for protein kinase C in the regulation of smooth muscle tone maintenance, particularly in vascular smooth muscle. Several possible signal transduction cascades involving protein kinase C are outlined. Increasing evidence suggests a link between protein kinase C and actin-based regulatory mechanisms. This review places emphasis on relating up-to-date biochemical facts to the physiological realities of the smooth muscle cell.

摘要

在过去二十年中,对分化的收缩性平滑肌组织进行的研究表明,20 kDa肌球蛋白轻链磷酸化对肌球蛋白的共价修饰是平滑肌收缩活动调节的一种重要方式,特别是在产生相性收缩和紧张性收缩的初始发展方面。与横纹肌相比,这种调节机制在平滑肌中似乎具有独特的重要性。然而,同样清楚的是,蛋白激酶C在平滑肌张力维持的调节中起着重要作用,特别是在血管平滑肌中。概述了几种涉及蛋白激酶C的可能信号转导级联反应。越来越多的证据表明蛋白激酶C与基于肌动蛋白的调节机制之间存在联系。本综述着重于将最新的生化事实与平滑肌细胞的生理实际情况联系起来。

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