Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chambers, Anna R, Aschauer, Dominik F, Eppler, Jens-Bastian, Kaschube, Matthias, Rumpel, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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
_version_ 1785035682449719296
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
work_keys_str_mv AT chambersannar astablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT aschauerdominikf astablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT epplerjensbastian astablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT kaschubematthias astablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT rumpelsimon astablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT chambersannar stablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT aschauerdominikf stablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT epplerjensbastian stablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT kaschubematthias stablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties
AT rumpelsimon stablesensorymapemergesfromadynamicequilibriumofneuronswithunstabletuningproperties