Spatial coding dysfunction and network instability in the aging medial entorhinal cortex

Across species, spatial memory declines with age, possibly reflecting altered hippocampal and medial entorhinal cortex (MEC) function. However, the integrity of cellular and network-level spatial coding in aged MEC is unknown. Here, we leveraged in vivo electrophysiology to assess MEC function in young, middle-aged, and aged mice navigating virtual environments. In aged grid cells, we observed impaired stabilization of context-specific spatial firing, correlated with spatial memory deficits. Additionally, aged grid networks shifted firing patterns often, but with poor alignment to context changes. Aged spatial firing was also unstable in an unchanging environment. In these same mice, we identified 458 genes differentially expressed with age in MEC, 61 of which had expression correlated with spatial coding quality. These genes were interneuron-enriched and related to synaptic plasticity, notably including a perineuronal net component. Together, these findings identify coordinated transcriptomic, cellular, and network changes in MEC implicated in impaired spatial memory in aging.

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Journal
Nature Communications
Published
2025-10-03
DOI
https://doi.org/10.1038/s41467-025-63229-0
Primary Topic
Memory and Neural Mechanisms
Type
article
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article

Spatial coding dysfunction and network instability in the aging medial entorhinal cortex

Karishma Pratt, Saul Villeda, Charlotte Herber, Jeremy M. Shea et al.
Nature Communications
Memory and Neural Mechanisms
article

Spatial coding dysfunction and network instability in the aging medial entorhinal cortex

Karishma Pratt, Saul Villeda, Charlotte Herber, Jeremy M. Shea, Lisa M. Giocomo
article en

Abstract

Across species, spatial memory declines with age, possibly reflecting altered hippocampal and medial entorhinal cortex (MEC) function. However, the integrity of cellular and network-level spatial coding in aged MEC is unknown. Here, we leveraged in vivo electrophysiology to assess MEC function in young, middle-aged, and aged mice navigating virtual environments. In aged grid cells, we observed impaired stabilization of context-specific spatial firing, correlated with spatial memory deficits. Additionally, aged grid networks shifted firing patterns often, but with poor alignment to context changes. Aged spatial firing was also unstable in an unchanging environment. In these same mice, we identified 458 genes differentially expressed with age in MEC, 61 of which had expression correlated with spatial coding quality. These genes were interneuron-enriched and related to synaptic plasticity, notably including a perineuronal net component. Together, these findings identify coordinated transcriptomic, cellular, and network changes in MEC implicated in impaired spatial memory in aging.

Nature CommunicationsVol. 16(1)
Howard Hughes Medical Institute (US), University of California, San Francisco (US), Institute on Aging (US), Stanford Medicine (US), Stanford University (US)
Openalex Percentile: Top 73%
Memory and Neural Mechanisms
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Spatial coding dysfunction and network instability in the aging medial entorhinal cortex — Karishma Pratt, Saul Villeda, et al. · Nature Communications (2025) | TGRS Research Map | TGRS