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Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans

Insulin signalling plays a significant role in both developmental programmes and pathways modulating the neuronal signalling that controls adult behaviour. Here, we have investigated insulin signalling in food-associated behaviour in adult C. elegans by scoring locomotion and feeding on and off bact...

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Autores principales: Dillon, James, Holden-Dye, Lindy, O’Connor, Vincent, Hopper, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875951/
https://www.ncbi.nlm.nih.gov/pubmed/27209024
http://dx.doi.org/10.1007/s10158-016-0187-2
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author Dillon, James
Holden-Dye, Lindy
O’Connor, Vincent
Hopper, Neil A.
author_facet Dillon, James
Holden-Dye, Lindy
O’Connor, Vincent
Hopper, Neil A.
author_sort Dillon, James
collection PubMed
description Insulin signalling plays a significant role in both developmental programmes and pathways modulating the neuronal signalling that controls adult behaviour. Here, we have investigated insulin signalling in food-associated behaviour in adult C. elegans by scoring locomotion and feeding on and off bacteria, the worm’s food. This analysis used mutants (daf-2, daf-18) of the insulin signalling pathway, and we provide evidence for an acute role for insulin signalling in the adult nervous system distinct from its impact on developmental programmes. Insulin receptor daf-2 mutants move slower than wild type both on and off food and showed impaired locomotory responses to food deprivation. This latter behaviour is manifest as a failure to instigate dispersal following prolonged food deprivation and suggests a role for insulin signalling in this adaptive response. Insulin receptor daf-2 mutants are also deficient in pharyngeal pumping on food and off food. Pharmacological analysis showed the pharynx of daf-2 is selectively compromised in its response to 5-HT compared to the excitatory neuropeptide FLP-17. By comparing the adaptive pharyngeal behaviour in intact worms and isolated pharyngeal preparations, we determined that an insulin-dependent signal extrinsic to the pharyngeal system is involved in feeding adaptation. Hence, we suggest that reactive insulin signalling modulates both locomotory foraging and pharyngeal pumping as the animal adapts to the absence of food. We discuss this in the context of insulin signalling directing a shift in the sensitivity of neurotransmitter systems to regulate the worm’s response to changes in food availability in the environment.
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spelling pubmed-48759512016-06-21 Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans Dillon, James Holden-Dye, Lindy O’Connor, Vincent Hopper, Neil A. Invert Neurosci Original Article Insulin signalling plays a significant role in both developmental programmes and pathways modulating the neuronal signalling that controls adult behaviour. Here, we have investigated insulin signalling in food-associated behaviour in adult C. elegans by scoring locomotion and feeding on and off bacteria, the worm’s food. This analysis used mutants (daf-2, daf-18) of the insulin signalling pathway, and we provide evidence for an acute role for insulin signalling in the adult nervous system distinct from its impact on developmental programmes. Insulin receptor daf-2 mutants move slower than wild type both on and off food and showed impaired locomotory responses to food deprivation. This latter behaviour is manifest as a failure to instigate dispersal following prolonged food deprivation and suggests a role for insulin signalling in this adaptive response. Insulin receptor daf-2 mutants are also deficient in pharyngeal pumping on food and off food. Pharmacological analysis showed the pharynx of daf-2 is selectively compromised in its response to 5-HT compared to the excitatory neuropeptide FLP-17. By comparing the adaptive pharyngeal behaviour in intact worms and isolated pharyngeal preparations, we determined that an insulin-dependent signal extrinsic to the pharyngeal system is involved in feeding adaptation. Hence, we suggest that reactive insulin signalling modulates both locomotory foraging and pharyngeal pumping as the animal adapts to the absence of food. We discuss this in the context of insulin signalling directing a shift in the sensitivity of neurotransmitter systems to regulate the worm’s response to changes in food availability in the environment. Springer Berlin Heidelberg 2016-05-21 2016 /pmc/articles/PMC4875951/ /pubmed/27209024 http://dx.doi.org/10.1007/s10158-016-0187-2 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Article
Dillon, James
Holden-Dye, Lindy
O’Connor, Vincent
Hopper, Neil A.
Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans
title Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans
title_full Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans
title_fullStr Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans
title_full_unstemmed Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans
title_short Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans
title_sort context-dependent regulation of feeding behaviour by the insulin receptor, daf-2, in caenorhabditis elegans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875951/
https://www.ncbi.nlm.nih.gov/pubmed/27209024
http://dx.doi.org/10.1007/s10158-016-0187-2
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