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Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task

Learning about positive and negative outcomes of actions is crucial for survival and underpinned by conserved circuits including the striatum. How associations between actions and outcomes are formed is not fully understood, particularly when the outcomes have mixed positive and negative features. W...

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Autores principales: Bloem, Bernard, Huda, Rafiq, Amemori, Ken-ichi, Abate, Alex S., Krishna, Gayathri, Wilson, Anna L., Carter, Cody W., Sur, Mriganka, Graybiel, Ann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941061/
https://www.ncbi.nlm.nih.gov/pubmed/35318343
http://dx.doi.org/10.1038/s41467-022-28983-5
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author Bloem, Bernard
Huda, Rafiq
Amemori, Ken-ichi
Abate, Alex S.
Krishna, Gayathri
Wilson, Anna L.
Carter, Cody W.
Sur, Mriganka
Graybiel, Ann M.
author_facet Bloem, Bernard
Huda, Rafiq
Amemori, Ken-ichi
Abate, Alex S.
Krishna, Gayathri
Wilson, Anna L.
Carter, Cody W.
Sur, Mriganka
Graybiel, Ann M.
author_sort Bloem, Bernard
collection PubMed
description Learning about positive and negative outcomes of actions is crucial for survival and underpinned by conserved circuits including the striatum. How associations between actions and outcomes are formed is not fully understood, particularly when the outcomes have mixed positive and negative features. We developed a novel foraging (‘bandit’) task requiring mice to maximize rewards while minimizing punishments. By 2-photon Ca(++) imaging, we monitored activity of visually identified anterodorsal striatal striosomal and matrix neurons. We found that action-outcome associations for reward and punishment were encoded in parallel in partially overlapping populations. Single neurons could, for one action, encode outcomes of opposing valence. Striosome compartments consistently exhibited stronger representations of reinforcement outcomes than matrix, especially for high reward or punishment prediction errors. These findings demonstrate multiplexing of action-outcome contingencies by single identified striatal neurons and suggest that striosomal neurons are particularly important in action-outcome learning.
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spelling pubmed-89410612022-04-08 Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task Bloem, Bernard Huda, Rafiq Amemori, Ken-ichi Abate, Alex S. Krishna, Gayathri Wilson, Anna L. Carter, Cody W. Sur, Mriganka Graybiel, Ann M. Nat Commun Article Learning about positive and negative outcomes of actions is crucial for survival and underpinned by conserved circuits including the striatum. How associations between actions and outcomes are formed is not fully understood, particularly when the outcomes have mixed positive and negative features. We developed a novel foraging (‘bandit’) task requiring mice to maximize rewards while minimizing punishments. By 2-photon Ca(++) imaging, we monitored activity of visually identified anterodorsal striatal striosomal and matrix neurons. We found that action-outcome associations for reward and punishment were encoded in parallel in partially overlapping populations. Single neurons could, for one action, encode outcomes of opposing valence. Striosome compartments consistently exhibited stronger representations of reinforcement outcomes than matrix, especially for high reward or punishment prediction errors. These findings demonstrate multiplexing of action-outcome contingencies by single identified striatal neurons and suggest that striosomal neurons are particularly important in action-outcome learning. Nature Publishing Group UK 2022-03-22 /pmc/articles/PMC8941061/ /pubmed/35318343 http://dx.doi.org/10.1038/s41467-022-28983-5 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bloem, Bernard
Huda, Rafiq
Amemori, Ken-ichi
Abate, Alex S.
Krishna, Gayathri
Wilson, Anna L.
Carter, Cody W.
Sur, Mriganka
Graybiel, Ann M.
Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
title Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
title_full Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
title_fullStr Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
title_full_unstemmed Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
title_short Multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
title_sort multiplexed action-outcome representation by striatal striosome-matrix compartments detected with a mouse cost-benefit foraging task
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941061/
https://www.ncbi.nlm.nih.gov/pubmed/35318343
http://dx.doi.org/10.1038/s41467-022-28983-5
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