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Video-oculography in Mice
Published on: July 19, 2012
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Interdigitating Modules for Visual Processing During Locomotion and Rest in Mouse V1
A M Meier1, R D D'Souza1, W Ji1
1Department of Neuroscience, Washington University School of Medicine, St. Louis, MO 63110; USA.
Biorxiv : the Preprint Server for Biology
|March 10, 2025
Summary
Locomotion differentially impacts visual cortex (V1) circuits. Strongly modulated cells cluster in M2- interpatches, suggesting distinct processing networks influenced by feedback connections and interneurons.
Area of Science:
- Neuroscience
- Visual System Processing
- Cortical Circuits
Background:
- Layer 1 of the primary visual cortex (V1) receives locomotion-related signals from the dorsal lateral geniculate (dLGN) and lateral posterior (LP) thalamic nuclei.
- These inputs target distinct regions within V1 Layer 1: dLGN to M2+ patches and LP to M2- interpatches, indicating segregated motion processing networks.
Purpose of the Study:
- To investigate differential activation of L2/3 neurons in V1 by locomotion under M2+ and M2- modules.
- To explore the role of feedback connections from higher cortical areas to V1 Layer 1 in modulating these responses.
Main Methods:
- Calcium imaging in head-fixed awake mice to monitor neuronal activity.
- Pathway tracing to identify feedback connections from cortical areas to V1.
- Analysis of neuronal activity modulation by locomotion and correlated variability.
Main Results:
- Locomotion strongly modulated cell clusters aligned with M2- interpatches, while M2+ patches showed weak modulation.
- M2- interpatch cells exhibited increased correlated variability across distant visual field sites, suggesting broader integration.
- Pathway tracing revealed looped, like-to-like networks involving MOs-, PM-, and RSP-projecting neurons and feedback to V1 Layer 1.
Conclusions:
- Distinct V1 Layer 1 networks process locomotion-related signals, with M2- interpatches showing stronger modulation and wider integration.
- Feedback connections from higher cortical areas and somatostatin (SST) interneurons likely shape these locomotion-modulated subnetworks within M2- interpatches.

