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High-throughput automated home-cage mesoscopic functional imaging of mouse cortex

Author

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  • Timothy H. Murphy

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

  • Jamie D. Boyd

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

  • Federico Bolaños

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

  • Matthieu P. Vanni

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

  • Gergely Silasi

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

  • Dirk Haupt

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

  • Jeff M. LeDue

    (Kinsmen Laboratory of Neurological Research, University of British Columbia
    Djavad Mowafaghian Centre for Brain Health, University of British Columbia)

Abstract

Mouse head-fixed behaviour coupled with functional imaging has become a powerful technique in rodent systems neuroscience. However, training mice can be time consuming and is potentially stressful for animals. Here we report a fully automated, open source, self-initiated head-fixation system for mesoscopic functional imaging in mice. The system supports five mice at a time and requires minimal investigator intervention. Using genetically encoded calcium indicator transgenic mice, we longitudinally monitor cortical functional connectivity up to 24 h per day in >7,000 self-initiated and unsupervised imaging sessions up to 90 days. The procedure provides robust assessment of functional cortical maps on the basis of both spontaneous activity and brief sensory stimuli such as light flashes. The approach is scalable to a number of remotely controlled cages that can be assessed within the controlled conditions of dedicated animal facilities. We anticipate that home-cage brain imaging will permit flexible and chronic assessment of mesoscale cortical function.

Suggested Citation

  • Timothy H. Murphy & Jamie D. Boyd & Federico Bolaños & Matthieu P. Vanni & Gergely Silasi & Dirk Haupt & Jeff M. LeDue, 2016. "High-throughput automated home-cage mesoscopic functional imaging of mouse cortex," Nature Communications, Nature, vol. 7(1), pages 1-12, September.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11611
    DOI: 10.1038/ncomms11611
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    Cited by:

    1. Dongsheng Xiao & Brandon J. Forys & Matthieu P. Vanni & Timothy H. Murphy, 2021. "MesoNet allows automated scaling and segmentation of mouse mesoscale cortical maps using machine learning," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
    2. Liang Shi & Xiaoxi Fu & Shen Gui & Tong Wan & Junjie Zhuo & Jinling Lu & Pengcheng Li, 2024. "Global spatiotemporal synchronizing structures of spontaneous neural activities in different cell types," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    3. P. Dylan Rich & Stephan Yves Thiberge & Benjamin B. Scott & Caiying Guo & D. Gowanlock R. Tervo & Carlos D. Brody & Alla Y. Karpova & Nathaniel D. Daw & David W. Tank, 2024. "Magnetic voluntary head-fixation in transgenic rats enables lifespan imaging of hippocampal neurons," Nature Communications, Nature, vol. 15(1), pages 1-13, December.

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