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Multicore fiber optic imaging reveals that astrocyte calcium activity in the mouse cerebral cortex is modulated by internal motivational state

Author

Listed:
  • Yung-Tian A. Gau

    (Johns Hopkins University)

  • Eric T. Hsu

    (Johns Hopkins University)

  • Richard J. Cha

    (Johns Hopkins University)

  • Rebecca W. Pak

    (Johns Hopkins University)

  • Loren L. Looger

    (University of California San Diego)

  • Jin U. Kang

    (Johns Hopkins University
    Johns Hopkins University)

  • Dwight E. Bergles

    (Johns Hopkins University
    Johns Hopkins University)

Abstract

Astrocytes are a direct target of neuromodulators and can influence neuronal activity on broad spatial and temporal scales in response to a rise in cytosolic calcium. However, our knowledge about how astrocytes are recruited during different animal behaviors remains limited. To measure astrocyte activity calcium in vivo during normative behaviors, we utilize a high-resolution, long working distance multicore fiber optic imaging system that allows visualization of individual astrocyte calcium transients in the cerebral cortex of freely moving mice. We define the spatiotemporal dynamics of astrocyte calcium changes during diverse behaviors, ranging from sleep-wake cycles to the exploration of novel objects, showing that their activity is more variable and less synchronous than apparent in head-immobilized imaging conditions. In accordance with their molecular diversity, individual astrocytes often exhibit distinct thresholds and activity patterns during explorative behaviors, allowing temporal encoding across the astrocyte network. Astrocyte calcium events were induced by noradrenergic and cholinergic systems and modulated by internal state. The distinct activity patterns exhibited by astrocytes provides a means to vary their neuromodulatory influence in different behavioral contexts and internal states.

Suggested Citation

  • Yung-Tian A. Gau & Eric T. Hsu & Richard J. Cha & Rebecca W. Pak & Loren L. Looger & Jin U. Kang & Dwight E. Bergles, 2024. "Multicore fiber optic imaging reveals that astrocyte calcium activity in the mouse cerebral cortex is modulated by internal motivational state," Nature Communications, Nature, vol. 15(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47345-x
    DOI: 10.1038/s41467-024-47345-x
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    References listed on IDEAS

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    1. Nicolas Vecoven & Damien Ernst & Antoine Wehenkel & Guillaume Drion, 2020. "Introducing neuromodulation in deep neural networks to learn adaptive behaviours," PLOS ONE, Public Library of Science, vol. 15(1), pages 1-13, January.
    2. Adi Doron & Alon Rubin & Aviya Benmelech-Chovav & Netai Benaim & Tom Carmi & Ron Refaeli & Nechama Novick & Tirzah Kreisel & Yaniv Ziv & Inbal Goshen, 2022. "Hippocampal astrocytes encode reward location," Nature, Nature, vol. 609(7928), pages 772-778, September.
    3. Colin Lever & Tom Wills & Francesca Cacucci & Neil Burgess & John O'Keefe, 2002. "Long-term plasticity in hippocampal place-cell representation of environmental geometry," Nature, Nature, vol. 416(6876), pages 90-94, March.
    4. Letizia Mariotti & Gabriele Losi & Annamaria Lia & Marcello Melone & Angela Chiavegato & Marta Gómez-Gonzalo & Michele Sessolo & Serena Bovetti & Angelo Forli & Micaela Zonta & Linda Maria Requie & Ia, 2018. "Interneuron-specific signaling evokes distinctive somatostatin-mediated responses in adult cortical astrocytes," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
    5. Laura Bojarskaite & Daniel M. Bjørnstad & Klas H. Pettersen & Céline Cunen & Gudmund Horn Hermansen & Knut Sindre Åbjørsbråten & Anna R. Chambers & Rolf Sprengel & Koen Vervaeke & Wannan Tang & Rune E, 2020. "Astrocytic Ca2+ signaling is reduced during sleep and is involved in the regulation of slow wave sleep," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
    6. Verena Untiet & Felix R. M. Beinlich & Peter Kusk & Ning Kang & Antonio Ladrón-de-Guevara & Wei Song & Celia Kjaerby & Mie Andersen & Natalie Hauglund & Zuzanna Bojarowska & Björn Sigurdsson & Saiyue , 2023. "Astrocytic chloride is brain state dependent and modulates inhibitory neurotransmission in mice," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    7. Lin Xu & Roger Anwyl & Michael J. Rowan, 1998. "Spatial exploration induces a persistent reversal of long-term potentiation in rat hippocampus," Nature, Nature, vol. 394(6696), pages 891-894, August.
    8. Benjamien Moeyaert & Graham Holt & Rajtarun Madangopal & Alberto Perez-Alvarez & Brenna C. Fearey & Nicholas F. Trojanowski & Julia Ledderose & Timothy A. Zolnik & Aniruddha Das & Davina Patel & Timot, 2018. "Improved methods for marking active neuron populations," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
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