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The developmental profile of visual cortex astrocytes

We investigated how astrocytes in layer 5 mouse visual cortex mature over postnatal days (P) 3–50. Across this age range, resting membrane potential increased, input resistance decreased, and membrane responses became more passive with age. Two-photon (2p) and confocal imaging of dye-loaded cells re...

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Detalles Bibliográficos
Autores principales: Watanabe, Airi, Guo, Connie, Sjöström, Per Jesper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212985/
https://www.ncbi.nlm.nih.gov/pubmed/37250801
http://dx.doi.org/10.1016/j.isci.2023.106828
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author Watanabe, Airi
Guo, Connie
Sjöström, Per Jesper
author_facet Watanabe, Airi
Guo, Connie
Sjöström, Per Jesper
author_sort Watanabe, Airi
collection PubMed
description We investigated how astrocytes in layer 5 mouse visual cortex mature over postnatal days (P) 3–50. Across this age range, resting membrane potential increased, input resistance decreased, and membrane responses became more passive with age. Two-photon (2p) and confocal imaging of dye-loaded cells revealed that gap-junction coupling increased starting ∼P7. Morphological reconstructions revealed increased branch density but shorter branches after P20, suggesting that astrocyte branches may get pruned as tiling is established. Finally, we visualized spontaneous Ca(2+) transients with 2p microscopy and found that Ca(2+) events decorrelated, became more frequent and briefer with age. As astrocytes mature, spontaneous Ca(2+) activity thus changes from relatively cell-wide, synchronous waves to local transients. Several astrocyte properties were stably mature from ∼P15, coinciding with eye opening, although morphology continued to develop. Our findings provide a descriptive foundation of astrocyte maturation, useful for the study of astrocytic impact on visual cortex critical period plasticity.
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spelling pubmed-102129852023-05-27 The developmental profile of visual cortex astrocytes Watanabe, Airi Guo, Connie Sjöström, Per Jesper iScience Article We investigated how astrocytes in layer 5 mouse visual cortex mature over postnatal days (P) 3–50. Across this age range, resting membrane potential increased, input resistance decreased, and membrane responses became more passive with age. Two-photon (2p) and confocal imaging of dye-loaded cells revealed that gap-junction coupling increased starting ∼P7. Morphological reconstructions revealed increased branch density but shorter branches after P20, suggesting that astrocyte branches may get pruned as tiling is established. Finally, we visualized spontaneous Ca(2+) transients with 2p microscopy and found that Ca(2+) events decorrelated, became more frequent and briefer with age. As astrocytes mature, spontaneous Ca(2+) activity thus changes from relatively cell-wide, synchronous waves to local transients. Several astrocyte properties were stably mature from ∼P15, coinciding with eye opening, although morphology continued to develop. Our findings provide a descriptive foundation of astrocyte maturation, useful for the study of astrocytic impact on visual cortex critical period plasticity. Elsevier 2023-05-06 /pmc/articles/PMC10212985/ /pubmed/37250801 http://dx.doi.org/10.1016/j.isci.2023.106828 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Watanabe, Airi
Guo, Connie
Sjöström, Per Jesper
The developmental profile of visual cortex astrocytes
title The developmental profile of visual cortex astrocytes
title_full The developmental profile of visual cortex astrocytes
title_fullStr The developmental profile of visual cortex astrocytes
title_full_unstemmed The developmental profile of visual cortex astrocytes
title_short The developmental profile of visual cortex astrocytes
title_sort developmental profile of visual cortex astrocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212985/
https://www.ncbi.nlm.nih.gov/pubmed/37250801
http://dx.doi.org/10.1016/j.isci.2023.106828
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