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通过冷冻CLEM引导的冷冻电镜断层扫描可视化的记忆印迹突触三维分子结构。

Memory engram synapse 3D molecular architecture visualized by cryoCLEM-guided cryoET.

作者信息

Lovatt Charlie, O'Sullivan Thomas J, Luis Clara Ortega-de San, Ryan Tomás J, Frank René A W

机构信息

Astbury Centre for Structural Biology, School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom.

School of Biochemistry and Immunology, Trinity College Dublin, Dublin, Ireland.

出版信息

bioRxiv. 2025 Jan 12:2025.01.09.632151. doi: 10.1101/2025.01.09.632151.

DOI:10.1101/2025.01.09.632151
PMID:39829918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11741270/
Abstract

Memory is incorporated into the brain as physicochemical changes to engram cells. These are neuronal populations that form complex neuroanatomical circuits, are modified by experiences to store information, and allow for memory recall. At the molecular level, learning modifies synaptic communication to rewire engram circuits, a mechanism known as synaptic plasticity. However, despite its functional role on memory formation, the 3D molecular architecture of synapses within engram circuits is unknown. Here, we demonstrate the use of engram labelling technology and cryogenic correlated light and electron microscopy (cryoCLEM)-guided cryogenic electron tomography (cryoET) to visualize the in-tissue 3D molecular architecture of engram synapses of a contextual fear memory within the CA1 region of the mouse hippocampus. Engram cells exhibited structural diversity of macromolecular constituents and organelles in both pre- and postsynaptic compartments and within the synaptic cleft, including in clusters of membrane proteins, synaptic vesicle occupancy, and F-actin copy number. This 'engram to tomogram' approach, harnessing functional neuroscience and structural biology, provides a methodological framework for testing fundamental molecular plasticity mechanisms within engram circuits during memory encoding, storage and recall.

摘要

记忆作为对记忆细胞的物理化学变化被整合到大脑中。这些是形成复杂神经解剖回路的神经元群体,通过经验进行修饰以存储信息,并允许记忆回忆。在分子水平上,学习会改变突触通讯以重新连接记忆回路,这一机制被称为突触可塑性。然而,尽管其在记忆形成中具有功能作用,但记忆回路中突触的三维分子结构尚不清楚。在这里,我们展示了使用记忆标记技术以及低温相关光电子显微镜(cryoCLEM)引导的低温电子断层扫描(cryoET)来可视化小鼠海马体CA1区域内情境恐惧记忆的记忆突触在组织内的三维分子结构。记忆细胞在突触前和突触后隔室以及突触间隙中均表现出大分子成分和细胞器的结构多样性,包括膜蛋白簇、突触小泡占有率和F-肌动蛋白拷贝数。这种“从记忆到断层扫描”的方法,利用功能神经科学和结构生物学,为测试记忆编码、存储和回忆过程中记忆回路内的基本分子可塑性机制提供了一个方法框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/5b90f203498b/nihpp-2025.01.09.632151v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/a795afbe6b1e/nihpp-2025.01.09.632151v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/59f5a3899efe/nihpp-2025.01.09.632151v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/90e5f4bb50d3/nihpp-2025.01.09.632151v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/5b90f203498b/nihpp-2025.01.09.632151v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/a795afbe6b1e/nihpp-2025.01.09.632151v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/59f5a3899efe/nihpp-2025.01.09.632151v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/90e5f4bb50d3/nihpp-2025.01.09.632151v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c51/11741270/5b90f203498b/nihpp-2025.01.09.632151v1-f0004.jpg

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