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The spatial and temporal structure of neural activity across the fly brain

What are the spatial and temporal scales of brainwide neuronal activity? We used swept, confocally-aligned planar excitation (SCAPE) microscopy to image all cells in a large volume of the brain of adult Drosophila with high spatiotemporal resolution while flies engaged in a variety of spontaneous be...

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Autores principales: Schaffer, Evan S., Mishra, Neeli, Whiteway, Matthew R., Li, Wenze, Vancura, Michelle B., Freedman, Jason, Patel, Kripa B., Voleti, Venkatakaushik, Paninski, Liam, Hillman, Elizabeth M. C., Abbott, L. F., Axel, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495430/
https://www.ncbi.nlm.nih.gov/pubmed/37696814
http://dx.doi.org/10.1038/s41467-023-41261-2
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author Schaffer, Evan S.
Mishra, Neeli
Whiteway, Matthew R.
Li, Wenze
Vancura, Michelle B.
Freedman, Jason
Patel, Kripa B.
Voleti, Venkatakaushik
Paninski, Liam
Hillman, Elizabeth M. C.
Abbott, L. F.
Axel, Richard
author_facet Schaffer, Evan S.
Mishra, Neeli
Whiteway, Matthew R.
Li, Wenze
Vancura, Michelle B.
Freedman, Jason
Patel, Kripa B.
Voleti, Venkatakaushik
Paninski, Liam
Hillman, Elizabeth M. C.
Abbott, L. F.
Axel, Richard
author_sort Schaffer, Evan S.
collection PubMed
description What are the spatial and temporal scales of brainwide neuronal activity? We used swept, confocally-aligned planar excitation (SCAPE) microscopy to image all cells in a large volume of the brain of adult Drosophila with high spatiotemporal resolution while flies engaged in a variety of spontaneous behaviors. This revealed neural representations of behavior on multiple spatial and temporal scales. The activity of most neurons correlated (or anticorrelated) with running and flailing over timescales that ranged from seconds to a minute. Grooming elicited a weaker global response. Significant residual activity not directly correlated with behavior was high dimensional and reflected the activity of small clusters of spatially organized neurons that may correspond to genetically defined cell types. These clusters participate in the global dynamics, indicating that neural activity reflects a combination of local and broadly distributed components. This suggests that microcircuits with highly specified functions are provided with knowledge of the larger context in which they operate.
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spelling pubmed-104954302023-09-13 The spatial and temporal structure of neural activity across the fly brain Schaffer, Evan S. Mishra, Neeli Whiteway, Matthew R. Li, Wenze Vancura, Michelle B. Freedman, Jason Patel, Kripa B. Voleti, Venkatakaushik Paninski, Liam Hillman, Elizabeth M. C. Abbott, L. F. Axel, Richard Nat Commun Article What are the spatial and temporal scales of brainwide neuronal activity? We used swept, confocally-aligned planar excitation (SCAPE) microscopy to image all cells in a large volume of the brain of adult Drosophila with high spatiotemporal resolution while flies engaged in a variety of spontaneous behaviors. This revealed neural representations of behavior on multiple spatial and temporal scales. The activity of most neurons correlated (or anticorrelated) with running and flailing over timescales that ranged from seconds to a minute. Grooming elicited a weaker global response. Significant residual activity not directly correlated with behavior was high dimensional and reflected the activity of small clusters of spatially organized neurons that may correspond to genetically defined cell types. These clusters participate in the global dynamics, indicating that neural activity reflects a combination of local and broadly distributed components. This suggests that microcircuits with highly specified functions are provided with knowledge of the larger context in which they operate. Nature Publishing Group UK 2023-09-11 /pmc/articles/PMC10495430/ /pubmed/37696814 http://dx.doi.org/10.1038/s41467-023-41261-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Schaffer, Evan S.
Mishra, Neeli
Whiteway, Matthew R.
Li, Wenze
Vancura, Michelle B.
Freedman, Jason
Patel, Kripa B.
Voleti, Venkatakaushik
Paninski, Liam
Hillman, Elizabeth M. C.
Abbott, L. F.
Axel, Richard
The spatial and temporal structure of neural activity across the fly brain
title The spatial and temporal structure of neural activity across the fly brain
title_full The spatial and temporal structure of neural activity across the fly brain
title_fullStr The spatial and temporal structure of neural activity across the fly brain
title_full_unstemmed The spatial and temporal structure of neural activity across the fly brain
title_short The spatial and temporal structure of neural activity across the fly brain
title_sort spatial and temporal structure of neural activity across the fly brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495430/
https://www.ncbi.nlm.nih.gov/pubmed/37696814
http://dx.doi.org/10.1038/s41467-023-41261-2
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