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海马神经元突触形成过程中nectin-1和l-afadin的时空定位

Temporal and spatial localization of nectin-1 and l-afadin during synaptogenesis in hippocampal neurons.

作者信息

Lim Seung T, Lim Kuei-Cheng, Giuliano Rita E, Federoff Howard J

机构信息

Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.

出版信息

J Comp Neurol. 2008 Mar 10;507(2):1228-44. doi: 10.1002/cne.21608.

Abstract

Nectins are cell adhesion molecules that, together with the intracellular binding partner afadin, mediate adhesion and signaling at a variety of intercellular junctions. In this work we studied the distribution of nectin-1 and afadin during hippocampal synapse formation using cultured primary hippocampal neurons. Nectin-1 and afadin cluster at developing synapses between hippocampal neurons. These nectin-afadin clusters uniformly colocalize with N-cadherin-catenin pairs, suggesting that formation of developing synapses involves participation of both bimolecular systems. Nectin-1 is initially expressed at excitatory and inhibitory synapses but is progressively lost at inhibitory synapses during their maturation. Treatment of neurons with actin depolymerizing agents disrupts the synaptically localized nectin-1 and afadin cluster at an early stage and elicits nectin-1 ectodomain shedding. These data indicate that the synaptic localization of nectin-1 and l-afadin are F-actin-dependent and that the shedding of nectin-1 is a mechanism contributing to synaptic plasticity.

摘要

NECTIN 是细胞粘附分子,与细胞内结合伴侣 afadin 一起,在多种细胞间连接中介导粘附和信号传导。在这项工作中,我们使用培养的原代海马神经元研究了海马突触形成过程中 nectin-1 和 afadin 的分布。NECTIN-1 和 afadin 在海马神经元之间发育中的突触处聚集。这些 nectin-afadin 簇与 N-钙粘蛋白-连环蛋白对均匀共定位,表明发育中突触的形成涉及这两个双分子系统的参与。NECTIN-1 最初在兴奋性和抑制性突触中表达,但在抑制性突触成熟过程中逐渐消失。用肌动蛋白解聚剂处理神经元会在早期破坏突触定位的 nectin-1 和 afadin 簇,并引发 nectin-1 胞外域脱落。这些数据表明,NECTIN-1 和 l-afadin 的突触定位依赖于 F-肌动蛋白,并且 nectin-1 的脱落是一种有助于突触可塑性的机制。

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