Neurexins and their ligands at inhibitory synapses.

IF 2.8 4区 医学 Q2 NEUROSCIENCES
Frontiers in Synaptic Neuroscience Pub Date : 2022-12-21 eCollection Date: 2022-01-01 DOI:10.3389/fnsyn.2022.1087238
Emma E Boxer, Jason Aoto
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引用次数: 0

Abstract

Since the discovery of neurexins (Nrxns) as essential and evolutionarily conserved synaptic adhesion molecules, focus has largely centered on their functional contributions to glutamatergic synapses. Recently, significant advances to our understanding of neurexin function at GABAergic synapses have revealed that neurexins can play pleiotropic roles in regulating inhibitory synapse maintenance and function in a brain-region and synapse-specific manner. GABAergic neurons are incredibly diverse, exhibiting distinct synaptic properties, sites of innervation, neuromodulation, and plasticity. Different classes of GABAergic neurons often express distinct repertoires of Nrxn isoforms that exhibit differential alternative exon usage. Further, Nrxn ligands can be differentially expressed and can display synapse-specific localization patterns, which may contribute to the formation of a complex trans-synaptic molecular code that establishes the properties of inhibitory synapse function and properties of local circuitry. In this review, we will discuss how Nrxns and their ligands sculpt synaptic inhibition in a brain-region, cell-type and synapse-specific manner.

Abstract Image

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Abstract Image

抑制性突触中的神经毒素及其配体
自从发现神经肽(Nrxns)是重要的、进化上保守的突触粘附分子以来,人们的注意力主要集中在它们对谷氨酸能突触的功能性贡献上。最近,我们对神经肽在 GABA 能突触中的功能的认识取得了重大进展,发现神经肽可以以脑区和突触特异性的方式在调节抑制性突触的维持和功能方面发挥多向作用。GABA 能神经元种类繁多,具有不同的突触特性、神经支配部位、神经调节和可塑性。不同类别的 GABA 能神经元通常表达不同的 Nrxn 异构体,这些 Nrxn 异构体表现出不同的替代外显子用法。此外,Nrxn 配体可以不同方式表达,并显示出突触特异性定位模式,这可能有助于形成复杂的跨突触分子代码,从而确定抑制性突触功能的特性和局部电路的特性。在这篇综述中,我们将讨论 Nrxns 及其配体如何以脑区、细胞类型和突触特异性的方式形成突触抑制。
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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来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
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