FGF 配体成为突触特性的潜在指定者。

Cellscience Pub Date : 2010-07-27
Kieran Jones, M Albert Basson
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引用次数: 0

摘要

中枢神经系统(CNS)由数万亿个相互连接的神经元组成。神经元之间细胞间接触的专门区域称为突触,信息通常以化学形式在此传递。在过去的十年中,我们对突触的分子性质、形成和维持的了解取得了前所未有的进展。一个仍然存在的主要问题是,如何建立突触特性,以确保在突触两侧协调招募正确的突触成分,从而使突触前侧积累的神经递质与突触后膜上的同源受体相匹配。直到最近,成纤维细胞生长因子(FGFs)一直被认为是突触能力的一般调节剂,因为它们能够增加突触蛋白的表达或促进神经元分支。最近的一项研究表明,兴奋性突触与抑制性突触的形成在很大程度上取决于突触后膜上存在的 FGF 配体的特性。这一观察结果表明,FGF 是参与决定突触特性的关键靶源性线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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FGF ligands emerge as potential specifiers of synaptic identity.

The central nervous system (CNS) consists of trillions of interconnected neurons. The specialised regions of intercellular contact between neurons where information, usually in chemical form, is transmitted are called synapses. The last decade has seen an unprecedented advance in our understanding of the molecular nature, formation and maintenance of synapses. A major question that remains is how synaptic identity is established to ensure the coordinated recruitment of the correct synaptic components on both sides of the synapse so that the neurotransmitter accumulating on the presynaptic side is matched with its cognate receptor on the postsynaptic membrane. Until recently, Fibroblast Growth Factors (FGFs) have been thought of as general regulators of synaptic aptitude through their ability to increase the expression of synaptic proteins or promote neurite branching. A recent study shows that the decision to form an excitatory vs. inhibitory synapse may to a large extent be determined by the identity of the FGF ligand present at the postsynaptic membrane. This observation establishes FGFs as key target-derived cues that are involved in determining synaptic identity.

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