Department of Neuroscience, University of Padova, via Gabelli 65, I-35121 Padova, Italy.
Department of Pharmacy and Center of Excellence for Biomedical Research, University of Genova, I-16126 Genova, Italy.
Rev Neurosci. 2018 Sep 25;29(7):703-726. doi: 10.1515/revneuro-2017-0087.
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.
受体-受体相互作用(RRIs)的提出拓宽了人们对 G 蛋白偶联受体(GPCR)在细胞间通讯动态中的作用的认识。RRIs 确实允许 GPCR 不仅作为单体,而且作为受体复合物发挥作用,其中传入信号的整合取决于形成复合物的原聚体的数量、空间排列和激活顺序。控制 GPCR 在受体复合物中功能相互作用的主要生化机制是原聚体结构域之间的直接变构相互作用。这些大分子组装的形成在调节信号通路和与其他膜蛋白相互作用方面具有几个生理意义。它还影响着连接组学这一新兴领域,因为它有助于设定和调整突触强度。此外,最近的证据表明,通过外泌体途径在细胞之间转移 GPCR 和 GPCR 复合物,可以使靶细胞识别/解码它们不表达相关受体的递质和/或调节剂。因此,这一过程也可能为神经回路的重新部署开辟新的途径。本文综述了 GPCR 复合物形成和功能的基本方面。