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Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment
Neocortex is classically divided into distinct areas, each specializing in different function, but all could benefit from reinforcement feedback to inform and update local processing. Yet it remains elusive how global signals like reward and punishment are represented in local cortical computations....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683790/ https://www.ncbi.nlm.nih.gov/pubmed/36416886 http://dx.doi.org/10.7554/eLife.78815 |
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author | Szadai, Zoltán Pi, Hyun-Jae Chevy, Quentin Ócsai, Katalin Albeanu, Dinu F Chiovini, Balázs Szalay, Gergely Katona, Gergely Kepecs, Adam Rózsa, Balázs |
author_facet | Szadai, Zoltán Pi, Hyun-Jae Chevy, Quentin Ócsai, Katalin Albeanu, Dinu F Chiovini, Balázs Szalay, Gergely Katona, Gergely Kepecs, Adam Rózsa, Balázs |
author_sort | Szadai, Zoltán |
collection | PubMed |
description | Neocortex is classically divided into distinct areas, each specializing in different function, but all could benefit from reinforcement feedback to inform and update local processing. Yet it remains elusive how global signals like reward and punishment are represented in local cortical computations. Previously, we identified a cortical neuron type, vasoactive intestinal polypeptide (VIP)-expressing interneurons, in auditory cortex that is recruited by behavioral reinforcers and mediates disinhibitory control by inhibiting other inhibitory neurons. As the same disinhibitory cortical circuit is present virtually throughout cortex, we wondered whether VIP neurons are likewise recruited by reinforcers throughout cortex. We monitored VIP neural activity in dozens of cortical regions using three-dimensional random access two-photon microscopy and fiber photometry while mice learned an auditory discrimination task. We found that reward and punishment during initial learning produce rapid, cortex-wide activation of most VIP interneurons. This global recruitment mode showed variations in temporal dynamics in individual neurons and across areas. Neither the weak sensory tuning of VIP interneurons in visual cortex nor their arousal state modulation was fully predictive of reinforcer responses. We suggest that the global response mode of cortical VIP interneurons supports a cell-type-specific circuit mechanism by which organism-level information about reinforcers regulates local circuit processing and plasticity. |
format | Online Article Text |
id | pubmed-9683790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-96837902022-11-24 Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment Szadai, Zoltán Pi, Hyun-Jae Chevy, Quentin Ócsai, Katalin Albeanu, Dinu F Chiovini, Balázs Szalay, Gergely Katona, Gergely Kepecs, Adam Rózsa, Balázs eLife Neuroscience Neocortex is classically divided into distinct areas, each specializing in different function, but all could benefit from reinforcement feedback to inform and update local processing. Yet it remains elusive how global signals like reward and punishment are represented in local cortical computations. Previously, we identified a cortical neuron type, vasoactive intestinal polypeptide (VIP)-expressing interneurons, in auditory cortex that is recruited by behavioral reinforcers and mediates disinhibitory control by inhibiting other inhibitory neurons. As the same disinhibitory cortical circuit is present virtually throughout cortex, we wondered whether VIP neurons are likewise recruited by reinforcers throughout cortex. We monitored VIP neural activity in dozens of cortical regions using three-dimensional random access two-photon microscopy and fiber photometry while mice learned an auditory discrimination task. We found that reward and punishment during initial learning produce rapid, cortex-wide activation of most VIP interneurons. This global recruitment mode showed variations in temporal dynamics in individual neurons and across areas. Neither the weak sensory tuning of VIP interneurons in visual cortex nor their arousal state modulation was fully predictive of reinforcer responses. We suggest that the global response mode of cortical VIP interneurons supports a cell-type-specific circuit mechanism by which organism-level information about reinforcers regulates local circuit processing and plasticity. eLife Sciences Publications, Ltd 2022-11-23 /pmc/articles/PMC9683790/ /pubmed/36416886 http://dx.doi.org/10.7554/eLife.78815 Text en © 2022, Szadai, Pi, Chevy et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Szadai, Zoltán Pi, Hyun-Jae Chevy, Quentin Ócsai, Katalin Albeanu, Dinu F Chiovini, Balázs Szalay, Gergely Katona, Gergely Kepecs, Adam Rózsa, Balázs Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment |
title | Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment |
title_full | Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment |
title_fullStr | Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment |
title_full_unstemmed | Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment |
title_short | Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment |
title_sort | cortex-wide response mode of vip-expressing inhibitory neurons by reward and punishment |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683790/ https://www.ncbi.nlm.nih.gov/pubmed/36416886 http://dx.doi.org/10.7554/eLife.78815 |
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