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脑中突触结合蛋白表达的区域及发育调控:突触功能分化的候选分子元件

Regional and developmental regulation of syntaphilin expression in the brain: a candidate molecular element of synaptic functional differentiation.

作者信息

Das Sunit, Boczan Judit, Gerwin Claudia, Zald Philip B, Sheng Zu-Hang

机构信息

Synaptic Function Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 36, Room 5A-23, 36 Convent Drive, Bethesda, MD 20892-4154, USA.

出版信息

Brain Res Mol Brain Res. 2003 Aug 19;116(1-2):38-49. doi: 10.1016/s0169-328x(03)00212-2.

Abstract

The conserved nature of the basic machinery underlying synaptic function makes it necessary to search for other factors--structural and molecular--that could account for the tremendous diversity found among synapses even within a single neuron. Syntaphilin is a presynaptic membrane protein previously described as a molecular clamp that controls free syntaxin-1A and dynamin-1 availability, and thereby regulates synaptic vesicle exocytosis and endocytosis at the nerve terminal. In this study, we report our finding that syntaphilin expression is developmentally regulated, and show that syntaphilin is expressed most prominently in the mature rat brain, in areas that have been previously characterized to undergo synaptic plastic change. We also find that syntaphilin undergoes divergent subcellular targeting to the mitochondrial outer membrane and the synaptic plasma membrane, giving rise to two neuronal subpopulations of the protein that are modified in their relative enrichment with synaptic maturation and with the formation of cell contacts. Finally, we demonstrate that syntaphilin expression is initiated with induction of neuronal differentiation in PC12 cells. Given its biochemical and functional properties, the spatially and temporally limited nature of syntaphilin expression provides evidence that syntaphilin could be a molecular element of synaptic functional differentiation.

摘要

突触功能基础基本机制的保守性使得有必要寻找其他因素——结构和分子方面的——来解释即使在单个神经元内突触之间也存在的巨大差异。突触素是一种突触前膜蛋白,先前被描述为一种分子钳,可控制游离的 syntaxin-1A 和发动蛋白-1 的可用性,从而调节神经末梢处的突触小泡胞吐作用和内吞作用。在本研究中,我们报告了我们的发现,即突触素的表达受发育调控,并表明突触素在成熟大鼠脑中表达最为显著,在先前已被表征为经历突触可塑性变化的区域。我们还发现突触素在亚细胞水平上靶向线粒体外膜和突触质膜,产生了该蛋白的两个神经元亚群,它们在相对丰度上随着突触成熟和细胞接触的形成而发生改变。最后,我们证明突触素的表达始于 PC12 细胞中神经元分化的诱导。鉴于其生化和功能特性,突触素表达在空间和时间上的有限性提供了证据,表明突触素可能是突触功能分化的分子元件。

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