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A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties
Recent long-term measurements of neuronal activity have revealed that, despite stability in large-scale topographic maps, the tuning properties of individual cortical neurons can undergo substantial reformatting over days. To shed light on this apparent contradiction, we captured the sound response...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152095/ https://www.ncbi.nlm.nih.gov/pubmed/36418925 http://dx.doi.org/10.1093/cercor/bhac445 |
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author | Chambers, Anna R Aschauer, Dominik F Eppler, Jens-Bastian Kaschube, Matthias Rumpel, Simon |
author_facet | Chambers, Anna R Aschauer, Dominik F Eppler, Jens-Bastian Kaschube, Matthias Rumpel, Simon |
author_sort | Chambers, Anna R |
collection | PubMed |
description | Recent long-term measurements of neuronal activity have revealed that, despite stability in large-scale topographic maps, the tuning properties of individual cortical neurons can undergo substantial reformatting over days. To shed light on this apparent contradiction, we captured the sound response dynamics of auditory cortical neurons using repeated 2-photon calcium imaging in awake mice. We measured sound-evoked responses to a set of pure tone and complex sound stimuli in more than 20,000 auditory cortex neurons over several days. We found that a substantial fraction of neurons dropped in and out of the population response. We modeled these dynamics as a simple discrete-time Markov chain, capturing the continuous changes in responsiveness observed during stable behavioral and environmental conditions. Although only a minority of neurons were driven by the sound stimuli at a given time point, the model predicts that most cells would at least transiently become responsive within 100 days. We observe that, despite single-neuron volatility, the population-level representation of sound frequency was stably maintained, demonstrating the dynamic equilibrium underlying the tonotopic map. Our results show that sensory maps are maintained by shifting subpopulations of neurons “sharing” the job of creating a sensory representation. |
format | Online Article Text |
id | pubmed-10152095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101520952023-05-03 A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties Chambers, Anna R Aschauer, Dominik F Eppler, Jens-Bastian Kaschube, Matthias Rumpel, Simon Cereb Cortex Original Article Recent long-term measurements of neuronal activity have revealed that, despite stability in large-scale topographic maps, the tuning properties of individual cortical neurons can undergo substantial reformatting over days. To shed light on this apparent contradiction, we captured the sound response dynamics of auditory cortical neurons using repeated 2-photon calcium imaging in awake mice. We measured sound-evoked responses to a set of pure tone and complex sound stimuli in more than 20,000 auditory cortex neurons over several days. We found that a substantial fraction of neurons dropped in and out of the population response. We modeled these dynamics as a simple discrete-time Markov chain, capturing the continuous changes in responsiveness observed during stable behavioral and environmental conditions. Although only a minority of neurons were driven by the sound stimuli at a given time point, the model predicts that most cells would at least transiently become responsive within 100 days. We observe that, despite single-neuron volatility, the population-level representation of sound frequency was stably maintained, demonstrating the dynamic equilibrium underlying the tonotopic map. Our results show that sensory maps are maintained by shifting subpopulations of neurons “sharing” the job of creating a sensory representation. Oxford University Press 2022-11-23 /pmc/articles/PMC10152095/ /pubmed/36418925 http://dx.doi.org/10.1093/cercor/bhac445 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com. 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 Chambers, Anna R Aschauer, Dominik F Eppler, Jens-Bastian Kaschube, Matthias Rumpel, Simon A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
title | A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
title_full | A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
title_fullStr | A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
title_full_unstemmed | A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
title_short | A stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
title_sort | stable sensory map emerges from a dynamic equilibrium of neurons with unstable tuning properties |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152095/ https://www.ncbi.nlm.nih.gov/pubmed/36418925 http://dx.doi.org/10.1093/cercor/bhac445 |
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