Mechanisms of memory-supporting neuronal dynamics in hippocampal area CA3

Hippocampal CA3 is central to memory formation and retrieval. Although various network mechanisms have been proposed, direct evidence is lacking. Using intracellular V<sub>m</sub> recordings and optogenetic manipulations in behaving mice, we found that CA3 place-field activity is produced by a symmetric form of behavioral timescale synaptic plasticity (BTSP) at recurrent synapses among CA3 pyramidal neurons but not at synapses from the dentate gyrus (DG). Additional manipulations revealed that excitatory input from the entorhinal cortex (EC) but not the DG was required to update place cell activity based on the animal's movement. These data were captured by a computational model that used BTSP and an external updating input to produce attractor dynamics under online learning conditions. Theoretical analyses further highlight the superior memory storage capacity of such networks, especially when dealing with correlated input patterns. This evidence elucidates the cellular and circuit mechanisms of learning and memory formation in the hippocampus.

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Publication Details

Journal
Cell
Published
2024-10-24
DOI
https://doi.org/10.1016/j.cell.2024.09.041
Citations
35
Primary Topic
Memory and Neural Mechanisms
Type
article
Field-Weighted Citation Impact
11.65

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article

Mechanisms of memory-supporting neuronal dynamics in hippocampal area CA3

Sandro Romani, John J. Briguglio, Jeffrey C. Magee, Yiding Li
35 citations
Cell
Memory and Neural Mechanisms
11.65
article

Mechanisms of memory-supporting neuronal dynamics in hippocampal area CA3

Sandro Romani, John J. Briguglio, Jeffrey C. Magee, Yiding Li
article en
35 citations

Abstract

Hippocampal CA3 is central to memory formation and retrieval. Although various network mechanisms have been proposed, direct evidence is lacking. Using intracellular V<sub>m</sub> recordings and optogenetic manipulations in behaving mice, we found that CA3 place-field activity is produced by a symmetric form of behavioral timescale synaptic plasticity (BTSP) at recurrent synapses among CA3 pyramidal neurons but not at synapses from the dentate gyrus (DG). Additional manipulations revealed that excitatory input from the entorhinal cortex (EC) but not the DG was required to update place cell activity based on the animal's movement. These data were captured by a computational model that used BTSP and an external updating input to produce attractor dynamics under online learning conditions. Theoretical analyses further highlight the superior memory storage capacity of such networks, especially when dealing with correlated input patterns. This evidence elucidates the cellular and circuit mechanisms of learning and memory formation in the hippocampus.

CellVol. 187(24)
Howard Hughes Medical Institute (US), Baylor College of Medicine (US), Janelia Research Campus (US)
Howard Hughes Medical Institute, Cullen Foundation
Openalex Percentile: Top 1%
Memory and Neural Mechanisms
11.65
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