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跨膜信号转导 G 蛋白偶联受体与其他信号转导途径的相互作用。

Integration of transmembrane signaling Cross-talk among G-protein-linked receptors and other signal transduction pathways.

机构信息

Departments of Medicine and Pharmacology, Division of Cardiology, University of Colorado Health Sciences Center, School of Medicine, Denver, CO 80262 USA.

出版信息

Trends Cardiovasc Med. 1993 May-Jun;3(3):85-92. doi: 10.1016/1050-1738(93)90029-6.

Abstract

The heart is a point of convergence for many transmembrane signal transduction pathways and, as such, exemplifies the complexities of sorting out their interactions. In the heart and cardiovascular system, hormone and neurotransmitter signals are propagated via G-protein-and non-G-protein-linked receptors. The receptors, in turn, are coupled to many effectors, including adenylylcyclases, phospholipases, and ion channels, as well as protein kinases and phosphatases. Integrating the information from numerous signaling pathways requires "cross-talk" among the different pathways. This article provides a perspective and attempts to describe in some detail what is known about a few of these interactions. Cross-talk from stimulatory to inhibitory adenylylcyclase pathways, from inhibitory to stimulatory adenylylcyclase pathways, from the adenylylcyclase to the phospholipase-C pathway, and from tyrosine kinase to G-protein-coupled receptors is described. Because of its central importance in the regulation of the cardiovascular system, and due to the availability of good model systems, the powerful responses mediated by the β-adrenergic receptor pathway serve as an excellent model to approach this subject.

摘要

心脏是许多跨膜信号转导途径的汇聚点,因此是阐明其相互作用复杂性的典范。在心脏和心血管系统中,激素和神经递质信号通过 G 蛋白和非 G 蛋白偶联受体传递。受体反过来又与许多效应器偶联,包括腺苷酸环化酶、磷脂酶和离子通道,以及蛋白激酶和磷酸酶。整合来自众多信号通路的信息需要不同通路之间的“串扰”。本文提供了一个视角,并试图详细描述其中一些相互作用的情况。描述了从刺激型到抑制型腺苷酸环化酶途径、从抑制型到刺激型腺苷酸环化酶途径、从腺苷酸环化酶到磷脂酶-C 途径以及从酪氨酸激酶到 G 蛋白偶联受体的串扰。由于其在心血管系统调节中的核心重要性,并且由于存在良好的模型系统,β-肾上腺素能受体途径介导的强大反应可作为研究该主题的理想模型。

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