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海马神经元突触形成过程中N-钙黏蛋白的重新分布。

N-cadherin redistribution during synaptogenesis in hippocampal neurons.

作者信息

Benson D L, Tanaka H

机构信息

Fishberg Research Center for Neurobiology, Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

J Neurosci. 1998 Sep 1;18(17):6892-904. doi: 10.1523/JNEUROSCI.18-17-06892.1998.

Abstract

Cadherins are homophilic adhesion molecules that, together with their intracellular binding partners the catenins, mediate adhesion and signaling at a variety of intercellular junctions. This study shows that neural (N)-cadherin and beta-catenin, an intracellular binding partner for the classic cadherins, are present in axons and dendrites before synapse formation and then cluster at developing synapses between hippocampal neurons. N-cadherin is expressed initially at all synaptic sites but rapidly becomes restricted to a subpopulation of excitatory synaptic sites. Sites of GABAergic, inhibitory synapses in mature cultures therefore lack N-cadherin but are associated with clusters of beta-catenin, implying that they contain a different classic cadherin. These findings indicate that N-cadherin adhesion may stabilize early synapses that can then be remodeled to express a different cadherin and that cadherins systematically differentiate between functionally (excitatory and inhibitory) and spatially distinct synaptic sites on single neurons. These results suggest that differential cadherin expression may orchestrate the point-to-point specificity displayed by developing synapses.

摘要

钙黏着蛋白是同嗜性黏附分子,它们与其细胞内结合伴侣连环蛋白一起,在多种细胞间连接中介导黏附与信号传导。本研究表明,神经(N)-钙黏着蛋白和β-连环蛋白(经典钙黏着蛋白的细胞内结合伴侣)在突触形成之前就存在于轴突和树突中,然后聚集在海马神经元之间发育中的突触处。N-钙黏着蛋白最初在所有突触位点表达,但很快就局限于兴奋性突触位点的一个亚群。因此,成熟培养物中GABA能抑制性突触位点缺乏N-钙黏着蛋白,但与β-连环蛋白簇相关,这意味着它们含有不同的经典钙黏着蛋白。这些发现表明,N-钙黏着蛋白黏附可能会稳定早期突触,然后这些突触可以被重塑以表达不同的钙黏着蛋白,并且钙黏着蛋白在单个神经元上功能(兴奋性和抑制性)和空间上不同的突触位点之间进行系统性区分。这些结果表明,不同的钙黏着蛋白表达可能协调发育中突触所显示的点对点特异性。

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