• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

受体在突触膜和突触外膜之间的表面转运:然而它们确实在移动!

Surface trafficking of receptors between synaptic and extrasynaptic membranes: and yet they do move!

作者信息

Triller Antoine, Choquet Daniel

机构信息

INSERM UR497, Ecole Normale Supérieure, 46 Rue d'Ulm, Paris F75005, France.

出版信息

Trends Neurosci. 2005 Mar;28(3):133-9. doi: 10.1016/j.tins.2005.01.001.

DOI:10.1016/j.tins.2005.01.001
PMID:15749166
Abstract

Concentration of neurotransmitter receptors at synapses is thought to result from stable binding to subsynaptic scaffold proteins. Recent data on synaptic plasticity have shown that changes in synaptic strength derive partly from modification of postsynaptic receptor numbers. This has led to the notion of receptor trafficking into and out of synapses. The proposed underlying mechanisms have under-evaluated the role of extrasynaptic receptors. Recent technological advances have allowed imaging of receptor movements at the single-molecule level, and these experiments demonstrate that receptors switch at unexpected rates between extrasynaptic and synaptic localizations by lateral diffusion. Variation in receptor numbers at postsynaptic sites is therefore likely to depend on regulation of diffusion by modification of the structure of the membrane and/or by transient interactions with scaffolding proteins. This review is part of the TINS Synaptic Connectivity series.

摘要

人们认为,神经递质受体在突触处的聚集是由于与突触下支架蛋白的稳定结合所致。最近关于突触可塑性的数据表明,突触强度的变化部分源于突触后受体数量的改变。这引发了受体进出突触的运输这一概念。所提出的潜在机制对突触外受体的作用评估不足。最近的技术进步使得能够在单分子水平上对受体运动进行成像,这些实验表明,受体通过横向扩散以意想不到的速率在突触外和突触定位之间转换。因此,突触后位点受体数量的变化可能取决于通过改变膜结构和/或与支架蛋白的瞬时相互作用对扩散的调节。这篇综述是《神经科学趋势》突触连接系列的一部分。

相似文献

1
Surface trafficking of receptors between synaptic and extrasynaptic membranes: and yet they do move!受体在突触膜和突触外膜之间的表面转运:然而它们确实在移动!
Trends Neurosci. 2005 Mar;28(3):133-9. doi: 10.1016/j.tins.2005.01.001.
2
Molecular dynamics of postsynaptic receptors and scaffold proteins.突触后受体和支架蛋白的分子动力学
Curr Opin Neurobiol. 2008 Oct;18(5):532-40. doi: 10.1016/j.conb.2008.09.009. Epub 2008 Oct 23.
3
Dynamics of postsynaptic glutamate receptor targeting.突触后谷氨酸受体靶向的动力学
Curr Opin Neurobiol. 2007 Feb;17(1):53-8. doi: 10.1016/j.conb.2006.11.001. Epub 2006 Dec 11.
4
Modeling synaptic dynamics driven by receptor lateral diffusion.模拟由受体侧向扩散驱动的突触动力学。
Biophys J. 2006 Oct 1;91(7):2405-15. doi: 10.1529/biophysj.106.081935. Epub 2006 Jul 14.
5
Endosomal trafficking of AMPA-type glutamate receptors.AMPA 型谷氨酸受体的内体运输
Neuroscience. 2009 Jan 12;158(1):36-44. doi: 10.1016/j.neuroscience.2008.02.057. Epub 2008 Mar 6.
6
AMPA and NMDA glutamate receptor trafficking: multiple roads for reaching and leaving the synapse.α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和N-甲基-D-天冬氨酸(NMDA)谷氨酸受体转运:通往和离开突触的多条途径
Cell Tissue Res. 2006 Nov;326(2):423-38. doi: 10.1007/s00441-006-0254-9. Epub 2006 Jul 18.
7
Fast AMPAR trafficking for a high-frequency synaptic transmission.快速 AMPAR 转运实现高频突触传递。
Eur J Neurosci. 2010 Jul;32(2):250-60. doi: 10.1111/j.1460-9568.2010.07350.x. Epub 2010 Jul 14.
8
Regulation of AMPA receptors and synaptic plasticity.AMPA 受体的调节与突触可塑性
Neuroscience. 2009 Jan 12;158(1):105-25. doi: 10.1016/j.neuroscience.2008.02.037. Epub 2008 Feb 29.
9
Synaptic stability and plasticity in a floating world.漂浮世界中的突触稳定性和可塑性。
Curr Opin Neurobiol. 2010 Oct;20(5):631-9. doi: 10.1016/j.conb.2010.06.010. Epub 2010 Jul 23.
10
Measurement and characteristics of neurotransmitter receptor surface trafficking (Review).神经递质受体表面转运的测量与特性(综述)
Mol Membr Biol. 2008 May;25(4):344-52. doi: 10.1080/09687680801958364.

引用本文的文献

1
Amyloid-β-Driven Synaptic Deficits Are Mediated by Synaptic Removal of GluA3-Containing AMPA Receptors.淀粉样β蛋白引发的突触缺陷是由含GluA3的AMPA受体的突触清除介导的。
J Neurosci. 2025 Feb 26;45(9):e0393242024. doi: 10.1523/JNEUROSCI.0393-24.2024.
2
Information Load from Neuromediator Diffusion to Extrasynaptic Space: The Interplay between the Injection Frequency and Clearance.从神经递质扩散到突触外间隙的信息负载:注入频率与清除之间的相互作用。
Biology (Basel). 2024 Jul 26;13(8):566. doi: 10.3390/biology13080566.
3
Dysregulation of AMPA Receptor Trafficking and Intracellular Vesicular Sorting in the Prefrontal Cortex of Dopamine Transporter Knock-Out Rats.
多巴胺转运体敲除大鼠前额叶皮层 AMPA 受体运输和细胞内囊泡分拣失调。
Biomolecules. 2023 Mar 11;13(3):516. doi: 10.3390/biom13030516.
4
Trafficking proteins show limited differences in mobility across different postsynaptic spines.转运蛋白在不同突触后棘中的移动性差异有限。
iScience. 2023 Jan 13;26(2):105971. doi: 10.1016/j.isci.2023.105971. eCollection 2023 Feb 17.
5
mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function.代谢型谷氨酸受体 5(mGluR5)暂时局限在突触周纳米区室中,以形成突触功能。
Nat Commun. 2023 Jan 16;14(1):244. doi: 10.1038/s41467-022-35680-w.
6
Fluorescence microscopy imaging of a neurotransmitter receptor and its cell membrane lipid milieu.神经递质受体及其细胞膜脂质环境的荧光显微镜成像。
Front Mol Biosci. 2022 Nov 28;9:1014659. doi: 10.3389/fmolb.2022.1014659. eCollection 2022.
7
Specific motifs mediate post-synaptic and surface transport of G protein-coupled receptors.特定基序介导G蛋白偶联受体的突触后转运和表面转运。
iScience. 2021 Dec 18;25(1):103643. doi: 10.1016/j.isci.2021.103643. eCollection 2022 Jan 21.
8
Nanoscale Sub-Compartmentalization of the Dendritic Spine Compartment.树突棘亚区室的纳米级细分。
Biomolecules. 2021 Nov 15;11(11):1697. doi: 10.3390/biom11111697.
9
Lack of support for surface diffusion of postsynaptic AMPARs in tuning synaptic transmission.缺乏对突触后 AMPAR 表面扩散的支持,以调整突触传递。
Biophys J. 2021 Aug 17;120(16):3409-3417. doi: 10.1016/j.bpj.2021.06.026. Epub 2021 Jun 30.
10
Anti-NMDA receptor encephalitis: a review of mechanistic studies.抗N-甲基-D-天冬氨酸受体脑炎:机制研究综述
Int J Physiol Pathophysiol Pharmacol. 2021 Feb 15;13(1):1-11. eCollection 2021.