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

Memory is incorporated into the brain as physicochemical changes to engram cells. These neuronal populations form complex neuroanatomical circuits, are modified by experiences to store information, and allow memory recall. At the molecular level, learning modifies synaptic communication to rewire engram circuits. How macromolecules are organized within engram synapses is unknown. Here, we establish engram labeling technology combined with cryogenic correlated light and electron microscopy (cryoCLEM)-guided cryogenic electron tomography (cryoET) to visualize the in-tissue 3D macromolecular architecture of engram synapses of a contextual fear memory within the mouse hippocampus. Engram synapses exhibited structural diversity of macromolecular constituents and organelles in both pre- and postsynaptic compartments and within the synaptic cleft, including in membrane proteins, synaptic vesicle occupancy, and F-actin copy number. This "engram to tomogram" approach, harnessing in vivo functional neuroscience and structural biology, provides a methodological framework for testing fundamental molecular plasticity mechanisms within engram circuits.

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Publication Details

Journal
Structure
Published
2025-11-14
DOI
https://doi.org/10.1016/j.str.2025.10.014
Citations
1
Primary Topic
Advanced Electron Microscopy Techniques and Applications
Type
article
Field-Weighted Citation Impact
2.55
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article

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

C.J. Lovatt, Tomás J. Ryan, René Frank, Clara Ortega‐de San Luis et al.
1 citations
Structure
Advanced Electron Microscopy Techniques and Applications
2.55
article

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

C.J. Lovatt, Tomás J. Ryan, René Frank, Clara Ortega‐de San Luis, Thomas D. O’Sullivan
article en
1 citations

Abstract

Memory is incorporated into the brain as physicochemical changes to engram cells. These neuronal populations form complex neuroanatomical circuits, are modified by experiences to store information, and allow memory recall. At the molecular level, learning modifies synaptic communication to rewire engram circuits. How macromolecules are organized within engram synapses is unknown. Here, we establish engram labeling technology combined with cryogenic correlated light and electron microscopy (cryoCLEM)-guided cryogenic electron tomography (cryoET) to visualize the in-tissue 3D macromolecular architecture of engram synapses of a contextual fear memory within the mouse hippocampus. Engram synapses exhibited structural diversity of macromolecular constituents and organelles in both pre- and postsynaptic compartments and within the synaptic cleft, including in membrane proteins, synaptic vesicle occupancy, and F-actin copy number. This "engram to tomogram" approach, harnessing in vivo functional neuroscience and structural biology, provides a methodological framework for testing fundamental molecular plasticity mechanisms within engram circuits.

StructureVol. 34(1)
University of Leeds (GB)
Openalex Percentile: Top 8%
Advanced Electron Microscopy Techniques and Applications
2.55
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Memory engram synapse 3D macromolecular architecture visualized by cryoCLEM-guided cryoET — C.J. Lovatt, Tomás J. Ryan, et al. · Structure (2025) | TGRS Research Map | TGRS