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Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex
Action selection occurs through competition between potential choice options. Neural correlates of choice competition are observed across frontal cortex and downstream superior colliculus (SC) during decision-making, yet how these regions interact to mediate choice competition remains unresolved. He...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168218/ https://www.ncbi.nlm.nih.gov/pubmed/37162880 http://dx.doi.org/10.1101/2023.04.22.537884 |
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author | Thomas, Alyse Yang, Weiguo Wang, Catherine Tipparaju, Sri Laasya Chen, Guang Sullivan, Brennan Swiekatowski, Kylie Tatam, Mahima Gerfen, Charles Li, Nuo |
author_facet | Thomas, Alyse Yang, Weiguo Wang, Catherine Tipparaju, Sri Laasya Chen, Guang Sullivan, Brennan Swiekatowski, Kylie Tatam, Mahima Gerfen, Charles Li, Nuo |
author_sort | Thomas, Alyse |
collection | PubMed |
description | Action selection occurs through competition between potential choice options. Neural correlates of choice competition are observed across frontal cortex and downstream superior colliculus (SC) during decision-making, yet how these regions interact to mediate choice competition remains unresolved. Here we report that cell types within SC can bidirectionally modulate choice competition and drive choice activity in frontal cortex. In the mouse, topographically matched regions of frontal cortex and SC formed a descending motor pathway for directional licking and a re-entrant loop via the thalamus. During decision-making, distinct neuronal populations in both frontal cortex and SC encoded opposing lick directions and exhibited push-pull dynamics. SC GABAergic neurons encoded ipsilateral choice and glutamatergic neurons encoded contralateral choice, and activating or suppressing these cell types could bidirectionally drive push-pull choice activity in frontal cortex. These results thus identify SC as a major locus to modulate choice competition within the broader action selection network. |
format | Online Article Text |
id | pubmed-10168218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101682182023-05-10 Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex Thomas, Alyse Yang, Weiguo Wang, Catherine Tipparaju, Sri Laasya Chen, Guang Sullivan, Brennan Swiekatowski, Kylie Tatam, Mahima Gerfen, Charles Li, Nuo bioRxiv Article Action selection occurs through competition between potential choice options. Neural correlates of choice competition are observed across frontal cortex and downstream superior colliculus (SC) during decision-making, yet how these regions interact to mediate choice competition remains unresolved. Here we report that cell types within SC can bidirectionally modulate choice competition and drive choice activity in frontal cortex. In the mouse, topographically matched regions of frontal cortex and SC formed a descending motor pathway for directional licking and a re-entrant loop via the thalamus. During decision-making, distinct neuronal populations in both frontal cortex and SC encoded opposing lick directions and exhibited push-pull dynamics. SC GABAergic neurons encoded ipsilateral choice and glutamatergic neurons encoded contralateral choice, and activating or suppressing these cell types could bidirectionally drive push-pull choice activity in frontal cortex. These results thus identify SC as a major locus to modulate choice competition within the broader action selection network. Cold Spring Harbor Laboratory 2023-04-24 /pmc/articles/PMC10168218/ /pubmed/37162880 http://dx.doi.org/10.1101/2023.04.22.537884 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Thomas, Alyse Yang, Weiguo Wang, Catherine Tipparaju, Sri Laasya Chen, Guang Sullivan, Brennan Swiekatowski, Kylie Tatam, Mahima Gerfen, Charles Li, Nuo Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
title | Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
title_full | Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
title_fullStr | Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
title_full_unstemmed | Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
title_short | Superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
title_sort | superior colliculus cell types bidirectionally modulate choice activity in frontal cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168218/ https://www.ncbi.nlm.nih.gov/pubmed/37162880 http://dx.doi.org/10.1101/2023.04.22.537884 |
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