Functional Nano-segregation of Distinct Forms of Neurotransmission.

Q3 Neuroscience
Natalie J Guzikowski, Camille S Wang, Ege T Kavalali
{"title":"Functional Nano-segregation of Distinct Forms of Neurotransmission.","authors":"Natalie J Guzikowski, Camille S Wang, Ege T Kavalali","doi":"10.1007/978-3-032-12594-1_8","DOIUrl":null,"url":null,"abstract":"<p><p>Within the single micron of the synapse, three distinct modes of neurotransmission, driven by synchronous, asynchronous, and spontaneous neurotransmitter release, occur concurrently. In this chapter, we discuss the synaptic nano-organization comprised of neurotransmitter release machinery, molecular platforms, scaffolding proteins, and liquid complexes that support the discrete signaling of these three modes of neurotransmission. This robust nano-organization supports unique functional roles for each discrete mode at both excitatory glutamatergic and inhibitory GABAergic synapses. Modular nanocolumn organization of excitatory synapses and largely single-domain organization of inhibitory synapses maintain homeostatic plasticity within neural circuits. These recent findings support a basic design principle where the single synapse is a highly ordered and compartmentalized unit that by the functional nano-segregation of distinct forms of neurotransmission shapes synaptic efficacy, determines neurotransmission reliability, and tunes plasticity. The development of novel tools will be instrumental in further elucidating the nano-environment of the synapse, essential to both uncovering mechanisms underlying neurological disorders as well as their treatment.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"48 ","pages":"217-257"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in neurobiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-032-12594-1_8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 0

Abstract

Within the single micron of the synapse, three distinct modes of neurotransmission, driven by synchronous, asynchronous, and spontaneous neurotransmitter release, occur concurrently. In this chapter, we discuss the synaptic nano-organization comprised of neurotransmitter release machinery, molecular platforms, scaffolding proteins, and liquid complexes that support the discrete signaling of these three modes of neurotransmission. This robust nano-organization supports unique functional roles for each discrete mode at both excitatory glutamatergic and inhibitory GABAergic synapses. Modular nanocolumn organization of excitatory synapses and largely single-domain organization of inhibitory synapses maintain homeostatic plasticity within neural circuits. These recent findings support a basic design principle where the single synapse is a highly ordered and compartmentalized unit that by the functional nano-segregation of distinct forms of neurotransmission shapes synaptic efficacy, determines neurotransmission reliability, and tunes plasticity. The development of novel tools will be instrumental in further elucidating the nano-environment of the synapse, essential to both uncovering mechanisms underlying neurological disorders as well as their treatment.

不同形式神经传递的功能纳米分离。
在突触的一微米内,三种不同的神经传递模式同时发生,分别由同步、异步和自发的神经递质释放驱动。在本章中,我们讨论了由神经递质释放机制、分子平台、支架蛋白和支持这三种神经传递模式的离散信号的液体复合物组成的突触纳米组织。这种强大的纳米组织在兴奋性谷氨酸能和抑制性gaba能突触中支持每种离散模式的独特功能角色。兴奋性突触的模块化纳米柱组织和抑制性突触的单域组织维持了神经回路内的稳态可塑性。这些最近的发现支持了一个基本的设计原则,即单个突触是一个高度有序和划分的单位,通过不同形式的神经传递的功能纳米分离,形成突触的功效,决定神经传递的可靠性,并调节可塑性。新工具的开发将有助于进一步阐明突触的纳米环境,这对揭示神经系统疾病的潜在机制及其治疗都至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书