Burbach J Peter H, Meijer Dimphna H
Department of Translational Neuroscience, UMCU Brain Center, University Medical Center Utrecht, Utrecht, Netherlands.
Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Delft, Netherlands.
Front Neurosci. 2019 Jun 26;13:643. doi: 10.3389/fnins.2019.00643. eCollection 2019.
Latrophilins (LPHNs) are adhesion GPCRs that are originally discovered as spider's toxin receptors, but are now known to be involved in brain development and linked to several neuronal and non-neuronal disorders. Latrophilins act in conjunction with other cell adhesion molecules and may play a leading role in its network organization. Here, we focus on the main protein partners of latrophilins, namely teneurins, FLRTs and contactins and summarize their respective temporal and spatial expression patterns, links to neurodevelopmental disorders as well as their structural characteristics. We discuss how more recent insights into the separate cell biological functions of these proteins shed light on the central role of latrophilins in this network. We postulate that latrophilins control the refinement of synaptic properties of specific subtypes of neurons, requiring discrete combinations of proteins.
促胃液素释放肽受体(LPHNs)是粘附性G蛋白偶联受体,最初作为蜘蛛毒素受体被发现,但现在已知其参与大脑发育,并与多种神经和非神经疾病相关。促胃液素释放肽受体与其他细胞粘附分子协同作用,可能在其网络组织中起主导作用。在这里,我们重点关注促胃液素释放肽受体的主要蛋白质伴侣,即腱生蛋白、F3/contactin相关分子(FLRTs)和接触蛋白,并总结它们各自的时空表达模式、与神经发育障碍的联系以及它们的结构特征。我们讨论了对这些蛋白质各自细胞生物学功能的最新见解如何揭示促胃液素释放肽受体在这个网络中的核心作用。我们推测促胃液素释放肽受体控制特定亚型神经元突触特性的精细化,这需要蛋白质的离散组合。