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Recording large-scale, cellular-resolution neuronal activity from freely-moving mice

View ORCID ProfileAniruddha Das, Sarah Holden, Julie Borovicka, Jacob Icardi, Davina Patel, Rushik Patel, View ORCID ProfileJacob Raber, View ORCID ProfileHod Dana
doi: https://doi.org/10.1101/2022.06.01.494442
Aniruddha Das
1Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
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Sarah Holden
2Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon, USA
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Julie Borovicka
1Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
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Jacob Icardi
1Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
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Davina Patel
1Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
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Rushik Patel
1Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
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Jacob Raber
2Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon, USA
3Departments of Neurology, Psychiatry, and Radiation Medicine, Division of Neuroscience, ONPRC, Oregon Health and Science University, Portland, Oregon, USA
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Hod Dana
1Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
4Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine, School of Medicine, Case Western Reserve University, Cleveland, OH, USA
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  • For correspondence: danah@ccf.org
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Abstract

Current methods for recording large-scale neuronal activity from behaving mice with single-cell resolution require either fixing the mouse head under a microscope or attachment of a recording device to the animal’s skull. Both of these options significantly affect the animal behavior and hence also the recorded brain activity patterns. Here, we introduce a new method to acquire snapshots of single-cell cortical activity maps from freely-moving mice using a calcium sensor called CaMPARI. CaMPARI has a unique property of irreversibly changing its color from green to red inside active neurons when illuminated with 400nm light. We capitalize on this property to demonstrate cortex-wide activity recording without any head fixation or attachment of a miniaturized device to the mouse’s head. Multiple cortical regions were recorded while the mouse was performing a battery of behavioral and cognitive tests. We identified task-dependent activity patterns across motor and somatosensory cortices, with significant differences across sub-regions of the motor cortex. This new CaMPARI-based recording method expands the capabilities of recording neuronal activity from freely-moving and behaving mice under minimally-restrictive experimental conditions and provides large-scale volumetric data that are not accessible otherwise.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • More data were added in this version of the manuscript.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted September 18, 2022.
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Recording large-scale, cellular-resolution neuronal activity from freely-moving mice
Aniruddha Das, Sarah Holden, Julie Borovicka, Jacob Icardi, Davina Patel, Rushik Patel, Jacob Raber, Hod Dana
bioRxiv 2022.06.01.494442; doi: https://doi.org/10.1101/2022.06.01.494442
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Recording large-scale, cellular-resolution neuronal activity from freely-moving mice
Aniruddha Das, Sarah Holden, Julie Borovicka, Jacob Icardi, Davina Patel, Rushik Patel, Jacob Raber, Hod Dana
bioRxiv 2022.06.01.494442; doi: https://doi.org/10.1101/2022.06.01.494442

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