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Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale
Serotonin controls many aspects of animal behavior and cognition. But how serotonin acts on its diverse receptor types in neurons across the brain to modulate global activity and behavior is unknown. Here, we examine how serotonin release from a feeding-responsive neuron in C. elegans alters brain-w...
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/PMC9882198/ https://www.ncbi.nlm.nih.gov/pubmed/36711891 http://dx.doi.org/10.1101/2023.01.15.524132 |
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author | Dag, Ugur Nwabudike, Ijeoma Kang, Di Gomes, Matthew A. Kim, Jungsoo Atanas, Adam A. Bueno, Eric Estrem, Cassi Pugliese, Sarah Wang, Ziyu Towlson, Emma Flavell, Steven W. |
author_facet | Dag, Ugur Nwabudike, Ijeoma Kang, Di Gomes, Matthew A. Kim, Jungsoo Atanas, Adam A. Bueno, Eric Estrem, Cassi Pugliese, Sarah Wang, Ziyu Towlson, Emma Flavell, Steven W. |
author_sort | Dag, Ugur |
collection | PubMed |
description | Serotonin controls many aspects of animal behavior and cognition. But how serotonin acts on its diverse receptor types in neurons across the brain to modulate global activity and behavior is unknown. Here, we examine how serotonin release from a feeding-responsive neuron in C. elegans alters brain-wide activity to induce foraging behaviors, like slow locomotion and increased feeding. A comprehensive genetic analysis identifies three core serotonin receptors that collectively induce slow locomotion upon serotonin release and three others that interact with them to further modulate this behavior. The core receptors have different functional roles: some induce behavioral responses to sudden increases in serotonin release, whereas others induce responses to persistent release. Whole-brain calcium imaging reveals widespread serotonin-associated brain dynamics, impacting different behavioral networks in different ways. We map out all sites of serotonin receptor expression in the connectome, which, together with synaptic connectivity, helps predict serotonin-associated brain-wide activity changes. These results provide a global view of how serotonin acts at defined sites across a connectome to modulate brain-wide activity and behavior. |
format | Online Article Text |
id | pubmed-9882198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-98821982023-01-28 Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale Dag, Ugur Nwabudike, Ijeoma Kang, Di Gomes, Matthew A. Kim, Jungsoo Atanas, Adam A. Bueno, Eric Estrem, Cassi Pugliese, Sarah Wang, Ziyu Towlson, Emma Flavell, Steven W. bioRxiv Article Serotonin controls many aspects of animal behavior and cognition. But how serotonin acts on its diverse receptor types in neurons across the brain to modulate global activity and behavior is unknown. Here, we examine how serotonin release from a feeding-responsive neuron in C. elegans alters brain-wide activity to induce foraging behaviors, like slow locomotion and increased feeding. A comprehensive genetic analysis identifies three core serotonin receptors that collectively induce slow locomotion upon serotonin release and three others that interact with them to further modulate this behavior. The core receptors have different functional roles: some induce behavioral responses to sudden increases in serotonin release, whereas others induce responses to persistent release. Whole-brain calcium imaging reveals widespread serotonin-associated brain dynamics, impacting different behavioral networks in different ways. We map out all sites of serotonin receptor expression in the connectome, which, together with synaptic connectivity, helps predict serotonin-associated brain-wide activity changes. These results provide a global view of how serotonin acts at defined sites across a connectome to modulate brain-wide activity and behavior. Cold Spring Harbor Laboratory 2023-01-18 /pmc/articles/PMC9882198/ /pubmed/36711891 http://dx.doi.org/10.1101/2023.01.15.524132 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Dag, Ugur Nwabudike, Ijeoma Kang, Di Gomes, Matthew A. Kim, Jungsoo Atanas, Adam A. Bueno, Eric Estrem, Cassi Pugliese, Sarah Wang, Ziyu Towlson, Emma Flavell, Steven W. Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale |
title | Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale |
title_full | Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale |
title_fullStr | Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale |
title_full_unstemmed | Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale |
title_short | Dissecting the Functional Organization of the C. elegans Serotonergic System at Whole-Brain Scale |
title_sort | dissecting the functional organization of the c. elegans serotonergic system at whole-brain scale |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882198/ https://www.ncbi.nlm.nih.gov/pubmed/36711891 http://dx.doi.org/10.1101/2023.01.15.524132 |
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