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平滑肌中的信号转导与调节

Signal transduction and regulation in smooth muscle.

作者信息

Somlyo A P, Somlyo A V

机构信息

Department of Molecular Physiology and Biological Physics, University of Virginia Health Sciences Center, Charlottesville 22908.

出版信息

Nature. 1994 Nov 17;372(6503):231-6. doi: 10.1038/372231a0.

Abstract

Smooth muscle cells in the walls of many organs are vital for most bodily functions, and their abnormalities contribute to a range of diseases. Although based on a sliding-filament mechanism similar to that of striated muscles, contraction of smooth muscle is regulated by pharmacomechanical as well as by electromechanical coupling mechanisms. Recent studies have revealed previously unrecognized contractile regulatory processes, such as G-protein-coupled inhibition of myosin light-chain phosphatase, regulation of myosin light-chain kinase by other kinases, and the functional effects of smooth muscle myosin isoforms. Abnormalities of these regulatory mechanisms and isoform variations may contribute to diseases of smooth muscle, and the G-protein-coupled inhibition of protein phosphatase is also likely to be important in regulating non-muscle cell functions mediated by cytoplasmic myosin II.

摘要

许多器官壁中的平滑肌细胞对大多数身体功能至关重要,其异常会导致一系列疾病。尽管平滑肌的收缩基于与横纹肌类似的滑行丝机制,但它受药物机械耦合以及机电耦合机制的调节。最近的研究揭示了以前未被认识的收缩调节过程,如G蛋白偶联对肌球蛋白轻链磷酸酶的抑制、其他激酶对肌球蛋白轻链激酶的调节以及平滑肌肌球蛋白同工型的功能效应。这些调节机制的异常和同工型变异可能导致平滑肌疾病,并且G蛋白偶联对蛋白磷酸酶的抑制在调节由细胞质肌球蛋白II介导的非肌肉细胞功能中也可能很重要。

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