Increased excitatory synapse size in hippocampal place cells compared to silent cells
Open Access
- 5 June 2025
- journal article
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 122 (23)
Abstract
Neuronal activity in the hippocampus creates a cognitive map of space that is essential for navigation. In any given environment, a fraction of hippocampal pyramidal cells (PCs) is active at specific locations (place cells), others are sparsely active without spatial tuning, and a significant proportion of the PCs is entirely silent. The mechanisms underlying the vastly different activities of PCs in the rodent hippocampal CA1 area are unknown. Here, we measured the in vivo activity of CA1 PCs using two-photon [Ca 2+ ] imaging in head-restrained mice during navigation in a virtual corridor and then performed in vitro patch-clamp recording to probe their intrinsic electrical properties and anatomical investigation to characterize their input synapses. The active and passive electrical properties of PCs were similar between PCs with different prior in vivo activities. Perisomatic inhibitory synapse density was also comparable among PCs. The average dendritic spine density and spine head area did not correlate with the mean in vivo activity of PCs, but the size of the spines of place cells was significantly larger compared to that of silent cells. Our results are consistent with excitatory synaptic plasticity as a major mechanism underlying spatially tuned activity of place cells in hippocampal networks.Keywords
Funding Information
- EC | European Research Council (ERC-AG 787157)
- European Reseach Council (ERC-CoG 771849)
- Hungarian Academy of Sciences (NAP2022-I-1/2022)
- Hungarian Academy of Sciences (NAP2022-I-1/2022)
- HHMI (55008740)
This publication has 44 references indexed in Scilit:
- Excitability mediates allocation of pre-configured ensembles to a hippocampal engram supporting contextual conditioned threat in miceNeuron, 2024
- All-optical physiology resolves a synaptic basis for behavioral timescale plasticityCell, 2023
- Local feedback inhibition tightly controls rapid formation of hippocampal place fieldsNeuron, 2022
- The Statistical Structure of the Hippocampal Code for Space as a Function of Time, Context, and ValueCell, 2020
- A High-Resolution Method for Quantitative Molecular Analysis of Functionally Characterized Individual SynapsesCell Reports, 2020
- Manipulating Hippocampal Place Cell Activity by Single-Cell Stimulation in Freely Moving MiceCell Reports, 2018
- Intracellular Determinants of Hippocampal CA1 Place and Silent Cell Activity in a Novel EnvironmentNeuron, 2011
- Understanding memory through hippocampal remappingTrends in Neurosciences, 2008
- Sparse coding of sensory inputsCurrent Opinion in Neurobiology, 2004
- The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving ratBrain Research, 1971