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活动依赖性 AMPA 受体扩散捕获作为早期 LTP 表达的关键步骤。

Activity-dependent diffusion trapping of AMPA receptors as a key step for expression of early LTP.

机构信息

University of Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297 , Bordeaux F-33000, France.

University of Bordeaux, CNRS, INSERM, Bordeaux Imaging Center, BIC, UMS 3420, US 4 , Bordeaux F-33000, France.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2024 Jul 29;379(1906):20230220. doi: 10.1098/rstb.2023.0220. Epub 2024 Jun 10.

DOI:10.1098/rstb.2023.0220
PMID:38853553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11343219/
Abstract

This review focuses on the activity-dependent diffusion trapping of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) as a crucial mechanism for the expression of early long-term potentiation (LTP), a process central to learning and memory. Despite decades of research, the precise mechanisms by which LTP induction leads to an increase in AMPAR responses at synapses have been elusive. We review the different hypotheses that have been put forward to explain the increased AMPAR responsiveness during LTP. We discuss the dynamic nature of AMPAR complexes, including their constant turnover and activity-dependent modifications that affect their synaptic accumulation. We highlight a hypothesis suggesting that AMPARs are diffusively trapped at synapses through activity-dependent interactions with protein-based binding slots in the post-synaptic density (PSD), offering a potential explanation for the increased synaptic strength during LTP. Furthermore, we outline the challenges still to be addressed before we fully understand the functional roles and molecular mechanisms of AMPAR dynamic nanoscale organization in LTP. This article is part of a discussion meeting issue 'Long-term potentiation: 50 years on'.

摘要

这篇综述聚焦于 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体 (AMPAR) 的活动依赖性扩散捕获,作为早期长时程增强 (LTP) 表达的关键机制,而 LTP 是学习和记忆的核心过程。尽管经过几十年的研究,LTP 诱导导致突触处 AMPAR 反应增加的确切机制仍难以捉摸。我们回顾了为解释 LTP 期间 AMPAR 反应性增加而提出的不同假设。我们讨论了 AMPAR 复合物的动态性质,包括其不断的周转和活动依赖性修饰,这些修饰会影响它们在突触中的积累。我们强调了一个假设,即 AMPAR 通过与突触后密度 (PSD) 中基于蛋白质的结合槽的活动依赖性相互作用在突触处被扩散捕获,为 LTP 期间突触强度的增加提供了一个潜在的解释。此外,我们概述了在充分理解 LTP 中 AMPAR 动态纳米级组织的功能作用和分子机制之前仍需要解决的挑战。本文是关于“长时程增强:50 年回顾”的讨论会议的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/f20651d50960/rstb.2023.0220.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/b7c0b3075331/rstb.2023.0220.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/c4d05705567d/rstb.2023.0220.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/f20651d50960/rstb.2023.0220.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/b7c0b3075331/rstb.2023.0220.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/c4d05705567d/rstb.2023.0220.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6b/11343219/f20651d50960/rstb.2023.0220.f003.jpg

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