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To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility
The stability and flexibility of the functional parcellation of the cerebral cortex is fundamental to how familiar and novel information is both represented and stored. We leveraged new advances in Ca(2+) sensors and microscopy to understand the dynamics of functional segmentation in the dorsal cere...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233288/ https://www.ncbi.nlm.nih.gov/pubmed/36734268 http://dx.doi.org/10.1093/cercor/bhac523 |
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author | Nietz, Angela K Streng, Martha L Popa, Laurentiu S Carter, Russell E Flaherty, Evelyn B Aronson, Justin D Ebner, Timothy J |
author_facet | Nietz, Angela K Streng, Martha L Popa, Laurentiu S Carter, Russell E Flaherty, Evelyn B Aronson, Justin D Ebner, Timothy J |
author_sort | Nietz, Angela K |
collection | PubMed |
description | The stability and flexibility of the functional parcellation of the cerebral cortex is fundamental to how familiar and novel information is both represented and stored. We leveraged new advances in Ca(2+) sensors and microscopy to understand the dynamics of functional segmentation in the dorsal cerebral cortex. We performed wide-field Ca(2+) imaging in head-fixed mice and used spatial independent component analysis (ICA) to identify independent spatial sources of Ca(2+) fluorescence. The imaging data were evaluated over multiple timescales and discrete behaviors including resting, walking, and grooming. When evaluated over the entire dataset, a set of template independent components (ICs) were identified that were common across behaviors. Template ICs were present across a range of timescales, from days to 30 seconds, although with lower occurrence probability at shorter timescales, highlighting the stability of the functional segmentation. Importantly, unique ICs emerged at the shorter duration timescales that could act to transiently refine the cortical network. When data were evaluated by behavior, both common and behavior-specific ICs emerged. Each behavior is composed of unique combinations of common and behavior-specific ICs. These observations suggest that cerebral cortical functional segmentation exhibits considerable spatial stability over time and behaviors while retaining the flexibility for task-dependent reorganization. |
format | Online Article Text |
id | pubmed-10233288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102332882023-06-02 To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility Nietz, Angela K Streng, Martha L Popa, Laurentiu S Carter, Russell E Flaherty, Evelyn B Aronson, Justin D Ebner, Timothy J Cereb Cortex Original Article The stability and flexibility of the functional parcellation of the cerebral cortex is fundamental to how familiar and novel information is both represented and stored. We leveraged new advances in Ca(2+) sensors and microscopy to understand the dynamics of functional segmentation in the dorsal cerebral cortex. We performed wide-field Ca(2+) imaging in head-fixed mice and used spatial independent component analysis (ICA) to identify independent spatial sources of Ca(2+) fluorescence. The imaging data were evaluated over multiple timescales and discrete behaviors including resting, walking, and grooming. When evaluated over the entire dataset, a set of template independent components (ICs) were identified that were common across behaviors. Template ICs were present across a range of timescales, from days to 30 seconds, although with lower occurrence probability at shorter timescales, highlighting the stability of the functional segmentation. Importantly, unique ICs emerged at the shorter duration timescales that could act to transiently refine the cortical network. When data were evaluated by behavior, both common and behavior-specific ICs emerged. Each behavior is composed of unique combinations of common and behavior-specific ICs. These observations suggest that cerebral cortical functional segmentation exhibits considerable spatial stability over time and behaviors while retaining the flexibility for task-dependent reorganization. Oxford University Press 2023-02-02 /pmc/articles/PMC10233288/ /pubmed/36734268 http://dx.doi.org/10.1093/cercor/bhac523 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Nietz, Angela K Streng, Martha L Popa, Laurentiu S Carter, Russell E Flaherty, Evelyn B Aronson, Justin D Ebner, Timothy J To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
title | To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
title_full | To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
title_fullStr | To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
title_full_unstemmed | To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
title_short | To be and not to be: wide-field Ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
title_sort | to be and not to be: wide-field ca(2+) imaging reveals neocortical functional segmentation combines stability and flexibility |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233288/ https://www.ncbi.nlm.nih.gov/pubmed/36734268 http://dx.doi.org/10.1093/cercor/bhac523 |
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