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A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior
Neuromodulators promote adaptive behaviors that are often complex and involve concerted activity changes across circuits that are often not physically connected. It is not well understood how neuromodulatory systems accomplish these tasks. Here, we show that the Caenorhabditis elegans NLP-12 neurope...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626090/ https://www.ncbi.nlm.nih.gov/pubmed/34766905 http://dx.doi.org/10.7554/eLife.71747 |
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author | Ramachandran, Shankar Banerjee, Navonil Bhattacharya, Raja Lemons, Michele L Florman, Jeremy Lambert, Christopher M Touroutine, Denis Alexander, Kellianne Schoofs, Liliane Alkema, Mark J Beets, Isabel Francis, Michael M |
author_facet | Ramachandran, Shankar Banerjee, Navonil Bhattacharya, Raja Lemons, Michele L Florman, Jeremy Lambert, Christopher M Touroutine, Denis Alexander, Kellianne Schoofs, Liliane Alkema, Mark J Beets, Isabel Francis, Michael M |
author_sort | Ramachandran, Shankar |
collection | PubMed |
description | Neuromodulators promote adaptive behaviors that are often complex and involve concerted activity changes across circuits that are often not physically connected. It is not well understood how neuromodulatory systems accomplish these tasks. Here, we show that the Caenorhabditis elegans NLP-12 neuropeptide system shapes responses to food availability by modulating the activity of head and body wall motor neurons through alternate G-protein coupled receptor (GPCR) targets, CKR-1 and CKR-2. We show ckr-2 deletion reduces body bend depth during movement under basal conditions. We demonstrate CKR-1 is a functional NLP-12 receptor and define its expression in the nervous system. In contrast to basal locomotion, biased CKR-1 GPCR stimulation of head motor neurons promotes turning during local searching. Deletion of ckr-1 reduces head neuron activity and diminishes turning while specific ckr-1 overexpression or head neuron activation promote turning. Thus, our studies suggest locomotor responses to changing food availability are regulated through conditional NLP-12 stimulation of head or body wall motor circuits. |
format | Online Article Text |
id | pubmed-8626090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-86260902021-11-29 A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior Ramachandran, Shankar Banerjee, Navonil Bhattacharya, Raja Lemons, Michele L Florman, Jeremy Lambert, Christopher M Touroutine, Denis Alexander, Kellianne Schoofs, Liliane Alkema, Mark J Beets, Isabel Francis, Michael M eLife Neuroscience Neuromodulators promote adaptive behaviors that are often complex and involve concerted activity changes across circuits that are often not physically connected. It is not well understood how neuromodulatory systems accomplish these tasks. Here, we show that the Caenorhabditis elegans NLP-12 neuropeptide system shapes responses to food availability by modulating the activity of head and body wall motor neurons through alternate G-protein coupled receptor (GPCR) targets, CKR-1 and CKR-2. We show ckr-2 deletion reduces body bend depth during movement under basal conditions. We demonstrate CKR-1 is a functional NLP-12 receptor and define its expression in the nervous system. In contrast to basal locomotion, biased CKR-1 GPCR stimulation of head motor neurons promotes turning during local searching. Deletion of ckr-1 reduces head neuron activity and diminishes turning while specific ckr-1 overexpression or head neuron activation promote turning. Thus, our studies suggest locomotor responses to changing food availability are regulated through conditional NLP-12 stimulation of head or body wall motor circuits. eLife Sciences Publications, Ltd 2021-11-12 /pmc/articles/PMC8626090/ /pubmed/34766905 http://dx.doi.org/10.7554/eLife.71747 Text en © 2021, Ramachandran 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 Ramachandran, Shankar Banerjee, Navonil Bhattacharya, Raja Lemons, Michele L Florman, Jeremy Lambert, Christopher M Touroutine, Denis Alexander, Kellianne Schoofs, Liliane Alkema, Mark J Beets, Isabel Francis, Michael M A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
title | A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
title_full | A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
title_fullStr | A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
title_full_unstemmed | A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
title_short | A conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
title_sort | conserved neuropeptide system links head and body motor circuits to enable adaptive behavior |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626090/ https://www.ncbi.nlm.nih.gov/pubmed/34766905 http://dx.doi.org/10.7554/eLife.71747 |
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