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A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior

An organism's ability to thrive in changing environmental conditions requires the capacity for making flexible behavioral responses. Here we show that, in the nematode Caenorhabditis elegans, foraging responses to changes in food availability require nlp-12, a homolog of the mammalian neuropept...

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Autores principales: Bhattacharya, Raja, Touroutine, Denis, Barbagallo, Belinda, Climer, Jason, Lambert, Christopher M., Clark, Christopher M., Alkema, Mark J., Francis, Michael M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148232/
https://www.ncbi.nlm.nih.gov/pubmed/25167143
http://dx.doi.org/10.1371/journal.pgen.1004584
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author Bhattacharya, Raja
Touroutine, Denis
Barbagallo, Belinda
Climer, Jason
Lambert, Christopher M.
Clark, Christopher M.
Alkema, Mark J.
Francis, Michael M.
author_facet Bhattacharya, Raja
Touroutine, Denis
Barbagallo, Belinda
Climer, Jason
Lambert, Christopher M.
Clark, Christopher M.
Alkema, Mark J.
Francis, Michael M.
author_sort Bhattacharya, Raja
collection PubMed
description An organism's ability to thrive in changing environmental conditions requires the capacity for making flexible behavioral responses. Here we show that, in the nematode Caenorhabditis elegans, foraging responses to changes in food availability require nlp-12, a homolog of the mammalian neuropeptide cholecystokinin (CCK). nlp-12 expression is limited to a single interneuron (DVA) that is postsynaptic to dopaminergic neurons involved in food-sensing, and presynaptic to locomotory control neurons. NLP-12 release from DVA is regulated through the D1-like dopamine receptor DOP-1, and both nlp-12 and dop-1 are required for normal local food searching responses. nlp-12/CCK overexpression recapitulates characteristics of local food searching, and DVA ablation or mutations disrupting muscle acetylcholine receptor function attenuate these effects. Conversely, nlp-12 deletion reverses behavioral and functional changes associated with genetically enhanced muscle acetylcholine receptor activity. Thus, our data suggest that dopamine-mediated sensory information about food availability shapes foraging in a context-dependent manner through peptide modulation of locomotory output.
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spelling pubmed-41482322014-08-29 A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior Bhattacharya, Raja Touroutine, Denis Barbagallo, Belinda Climer, Jason Lambert, Christopher M. Clark, Christopher M. Alkema, Mark J. Francis, Michael M. PLoS Genet Research Article An organism's ability to thrive in changing environmental conditions requires the capacity for making flexible behavioral responses. Here we show that, in the nematode Caenorhabditis elegans, foraging responses to changes in food availability require nlp-12, a homolog of the mammalian neuropeptide cholecystokinin (CCK). nlp-12 expression is limited to a single interneuron (DVA) that is postsynaptic to dopaminergic neurons involved in food-sensing, and presynaptic to locomotory control neurons. NLP-12 release from DVA is regulated through the D1-like dopamine receptor DOP-1, and both nlp-12 and dop-1 are required for normal local food searching responses. nlp-12/CCK overexpression recapitulates characteristics of local food searching, and DVA ablation or mutations disrupting muscle acetylcholine receptor function attenuate these effects. Conversely, nlp-12 deletion reverses behavioral and functional changes associated with genetically enhanced muscle acetylcholine receptor activity. Thus, our data suggest that dopamine-mediated sensory information about food availability shapes foraging in a context-dependent manner through peptide modulation of locomotory output. Public Library of Science 2014-08-28 /pmc/articles/PMC4148232/ /pubmed/25167143 http://dx.doi.org/10.1371/journal.pgen.1004584 Text en © 2014 Bhattacharya et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bhattacharya, Raja
Touroutine, Denis
Barbagallo, Belinda
Climer, Jason
Lambert, Christopher M.
Clark, Christopher M.
Alkema, Mark J.
Francis, Michael M.
A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior
title A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior
title_full A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior
title_fullStr A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior
title_full_unstemmed A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior
title_short A Conserved Dopamine-Cholecystokinin Signaling Pathway Shapes Context–Dependent Caenorhabditis elegans Behavior
title_sort conserved dopamine-cholecystokinin signaling pathway shapes context–dependent caenorhabditis elegans behavior
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148232/
https://www.ncbi.nlm.nih.gov/pubmed/25167143
http://dx.doi.org/10.1371/journal.pgen.1004584
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