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同种受体在受体 - 受体相互作用中的作用,重点关注多巴胺同种受体复合物。

Role of iso-receptors in receptor-receptor interactions with a focus on dopamine iso-receptor complexes.

作者信息

Agnati Luigi F, Guidolin Diego, Cervetto Chiara, Borroto-Escuela Dasiel O, Fuxe Kjell

出版信息

Rev Neurosci. 2016 Jan;27(1):1-25. doi: 10.1515/revneuro-2015-0024.

Abstract

Intercellular and intracellular communication processes consist of signals and recognition/decoding apparatuses of these signals. In humans, the G protein-coupled receptor (GPCR) family represents the largest family of cell surface receptors. More than 30 years ago, it has been proposed that GPCR could form dimers or higher-order oligomers (receptor mosaics [RMs] at the plasma membrane level and receptor-receptor interactions [RRIs] have been proposed as a new integrative mechanism for chemical signals impinging on cell plasma membranes). The basic phenomena involved in RRIs are allostery and cooperativity of membrane receptors, and the present paper provides basic information concerning their relevance for the integrative functions of RMs. In this context, the possible role of iso-receptor RM is discussed (with a special focus on dopamine receptor subtypes and on some of the RMs they form with other dopamine iso-receptors), and it is proposed that two types of cooperativity, namely, homotropic and heterotropic cooperativity, could allow distinguishing two types of functionally different RMs. From a general point of view, the presence of iso-receptors and their topological organization within RMs allow the use of a reduced number of signals for the intercellular communication processes, since the target cells can recognize and decode the same signal in different ways. This theoretical aspect is further analyzed here by means of an analogy with artificial information systems. Thus, it is suggested that the 'multiplexer' and 'demultiplexer' concepts could, at least in part, model the role of RMs formed by iso-receptors in the information handling by the cell.

摘要

细胞间和细胞内通讯过程由信号以及这些信号的识别/解码装置组成。在人类中,G蛋白偶联受体(GPCR)家族是最大的细胞表面受体家族。30多年前,有人提出GPCR可能形成二聚体或更高阶的寡聚体(在质膜水平上的受体镶嵌体[RMs]以及受体-受体相互作用[RRIs]被认为是作用于细胞质膜的化学信号的一种新的整合机制)。RRIs所涉及的基本现象是膜受体的变构和协同性,本文提供了有关它们与RMs整合功能相关性的基本信息。在此背景下,讨论了同型受体RM的可能作用(特别关注多巴胺受体亚型以及它们与其他多巴胺同型受体形成的一些RMs),并提出两种协同性,即同促协同性和异促协同性,可能有助于区分两种功能不同的RMs。从一般观点来看,同型受体的存在及其在RMs中的拓扑组织允许在细胞间通讯过程中使用数量减少的信号,因为靶细胞可以以不同方式识别和解码相同信号。本文通过与人工信息系统的类比进一步分析了这一理论方面。因此,有人提出“多路复用器”和“多路分解器”概念至少可以部分模拟由同型受体形成的RMs在细胞信息处理中的作用。

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