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G protein-coupled receptor-receptor interactions give integrative dynamics to intercellular communication

机译:G蛋白偶联受体 - 受体相互作用为细胞间通信提供综合动态

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摘要

The proposal of receptor-receptor interactions (RRIs) in the early 1980s broadened the view on the role of G protein-coupled receptors (GPCR) in the dynamics of the intercellular communication. RRIs, indeed, allow GPCR to operate not only as monomers but also as receptor complexes, in which the integration of the incoming signals depends on the number, spatial arrangement, and order of activation of the protomers forming the complex. The main biochemical mechanisms controlling the functional interplay of GPCR in the receptor complexes are direct allosteric interactions between protomer domains. The formation of these macromolecular assemblies has several physiologic implications in terms of the modulation of the signaling pathways and interaction with other membrane proteins. It also impacts on the emerging field of connectomics, as it contributes to set and tune the synaptic strength. Furthermore, recent evidence suggests that the transfer of GPCR and GPCR complexes between cells via the exosome pathway could enable the target cells to recognize/decode transmitters and/or modulators for which they did not express the pertinent receptors. Thus, this process may also open the possibility of a new type of redeployment of neural circuits. The fundamental aspects of GPCR complex formation and function are the focus of the present review article.
机译:20世纪80年代初期受体受体相互作用(RRI)的提议拓宽了G蛋白偶联受体(GPCR)在细胞间通信的动态中的作用的观点。实际上,RRI允许GPCR不仅作为单体而且作为受体复合物操作,其中输入信号的整合取决于形成复合物的激活的数量,空间排列和激活的顺序。控制受体复合物中GPCR功能相互作用的主要生物化学机制是激素结构域之间的直接变构相互作用。这些大分子组件的形成在调节信号通路和与其他膜蛋白的相互作用方面具有若干生理学意义。它对新兴的ConnectMics领域也会影响,因为它有助于设置和调整突触强度。此外,最近的证据表明,通过外出途径的细胞之间的GPCR和GPCR复合物可以使靶细胞能够识别/解码的发射器和/或它们没有表达相关受体的调节剂。因此,该过程还可以打开神经电路的新型重新部署的可能性。 GPCR复杂的形成和功能的基本方面是本综述文章的重点。

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