Realistic coupling enables flexible macroscopic traveling waves in the mouse cortex

Traveling waves are ubiquitous in neuronal systems across different spatial scales. While microscopic and mesoscopic waves are relatively well studied, the emergence of macroscopic traveling waves remains less understood. Here, by modeling the mouse cortex using spatial transcriptomic and connectivity data, we show that realistic cortical connectivity can generate a significantly higher level of macroscopic traveling waves than artificial local and uniform connectivity across multiple oscillation frequency bands, with the strongest advantage appearing in the theta, alpha, and beta frequency bands. By probing the model in different dynamic regimes, we find that macroscopic wave activity depends on both network connectivity and excitatory coupling strength, with a non-monotonic dependence on coupling. Together, our work shows how flexible macroscopic traveling waves can emerge in the mouse cortex and offers a computational framework to further study traveling waves in the mouse brain at the single-cell level.

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Publication Details

Journal
eLife
Published
2026-09-04
DOI
https://doi.org/10.7554/elife.108208.3
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
0.00

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article

Realistic coupling enables flexible macroscopic traveling waves in the mouse cortex

Guanhua Sun, Ruby Kim, Daniel B. Forger, James Hazelden
eLife
Neural dynamics and brain function
article

Realistic coupling enables flexible macroscopic traveling waves in the mouse cortex

Guanhua Sun, Ruby Kim, Daniel B. Forger, James Hazelden
article en

Abstract

Traveling waves are ubiquitous in neuronal systems across different spatial scales. While microscopic and mesoscopic waves are relatively well studied, the emergence of macroscopic traveling waves remains less understood. Here, by modeling the mouse cortex using spatial transcriptomic and connectivity data, we show that realistic cortical connectivity can generate a significantly higher level of macroscopic traveling waves than artificial local and uniform connectivity across multiple oscillation frequency bands, with the strongest advantage appearing in the theta, alpha, and beta frequency bands. By probing the model in different dynamic regimes, we find that macroscopic wave activity depends on both network connectivity and excitatory coupling strength, with a non-monotonic dependence on coupling. Together, our work shows how flexible macroscopic traveling waves can emerge in the mouse cortex and offers a computational framework to further study traveling waves in the mouse brain at the single-cell level.

eLifeVol. 14
University of Michigan (US)
Army Research Office
Openalex Percentile: Top 9%
Neural dynamics and brain function
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