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SALM/Lrfn家族突触粘附分子

SALM/Lrfn Family Synaptic Adhesion Molecules.

作者信息

Lie Eunkyung, Li Yan, Kim Ryunhee, Kim Eunjoon

机构信息

Center for Synaptic Brain Dysfunctions, Institute for Basic Science (IBS), Daejeon, South Korea.

Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, South Korea.

出版信息

Front Mol Neurosci. 2018 Apr 5;11:105. doi: 10.3389/fnmol.2018.00105. eCollection 2018.

Abstract

Synaptic adhesion-like molecules (SALMs) are a family of cell adhesion molecules involved in regulating neuronal and synapse development that have also been implicated in diverse brain dysfunctions, including autism spectrum disorders (ASDs). SALMs, also known as leucine-rich repeat (LRR) and fibronectin III domain-containing (LRFN) proteins, were originally identified as a group of novel adhesion-like molecules that contain LRRs in the extracellular region as well as a PDZ domain-binding tail that couples to PSD-95, an abundant excitatory postsynaptic scaffolding protein. While studies over the last decade have steadily explored the basic properties and synaptic and neuronal functions of SALMs, a number of recent studies have provided novel insights into molecular, structural, functional and clinical aspects of SALMs. Here we summarize these findings and discuss how SALMs act in concert with other synaptic proteins to regulate synapse development and function.

摘要

突触黏附样分子(SALMs)是一类细胞黏附分子,参与调节神经元和突触发育,也与多种脑功能障碍有关,包括自闭症谱系障碍(ASD)。SALMs,也被称为富含亮氨酸重复序列(LRR)和纤连蛋白III结构域的蛋白(LRFN),最初被鉴定为一组新型黏附样分子,其在细胞外区域含有LRR以及与PSD-95(一种丰富的兴奋性突触后支架蛋白)偶联的PDZ结构域结合尾巴。虽然过去十年的研究一直在稳步探索SALMs的基本特性以及突触和神经元功能,但最近的一些研究为SALMs的分子、结构、功能和临床方面提供了新的见解。在这里,我们总结这些发现,并讨论SALMs如何与其他突触蛋白协同作用来调节突触发育和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e9/5895706/23cc4bf678de/fnmol-11-00105-g0001.jpg

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