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Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms
Biological homeostasis invokes modulatory responses aimed at stabilizing internal conditions. Using tunable photo- and mechano-stimulation, we identified two distinct categories of homeostatic responses during the sleep-like state of Caenorhabditis elegans (lethargus). In the presence of weak or no...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273442/ https://www.ncbi.nlm.nih.gov/pubmed/25474127 http://dx.doi.org/10.7554/eLife.04380 |
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author | Nagy, Stanislav Tramm, Nora Sanders, Jarred Iwanir, Shachar Shirley, Ian A Levine, Erel Biron, David |
author_facet | Nagy, Stanislav Tramm, Nora Sanders, Jarred Iwanir, Shachar Shirley, Ian A Levine, Erel Biron, David |
author_sort | Nagy, Stanislav |
collection | PubMed |
description | Biological homeostasis invokes modulatory responses aimed at stabilizing internal conditions. Using tunable photo- and mechano-stimulation, we identified two distinct categories of homeostatic responses during the sleep-like state of Caenorhabditis elegans (lethargus). In the presence of weak or no stimuli, extended motion caused a subsequent extension of quiescence. The neuropeptide Y receptor homolog, NPR-1, and an inhibitory neuropeptide known to activate it, FLP-18, were required for this process. In the presence of strong stimuli, the correlations between motion and quiescence were disrupted for several minutes but homeostasis manifested as an overall elevation of the time spent in quiescence. This response to strong stimuli required the function of the DAF-16/FOXO transcription factor in neurons, but not that of NPR-1. Conversely, response to weak stimuli did not require the function of DAF-16/FOXO. These findings suggest that routine homeostatic stabilization of sleep may be distinct from homeostatic compensation following a strong disturbance. DOI: http://dx.doi.org/10.7554/eLife.04380.001 |
format | Online Article Text |
id | pubmed-4273442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42734422015-01-29 Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms Nagy, Stanislav Tramm, Nora Sanders, Jarred Iwanir, Shachar Shirley, Ian A Levine, Erel Biron, David eLife Neuroscience Biological homeostasis invokes modulatory responses aimed at stabilizing internal conditions. Using tunable photo- and mechano-stimulation, we identified two distinct categories of homeostatic responses during the sleep-like state of Caenorhabditis elegans (lethargus). In the presence of weak or no stimuli, extended motion caused a subsequent extension of quiescence. The neuropeptide Y receptor homolog, NPR-1, and an inhibitory neuropeptide known to activate it, FLP-18, were required for this process. In the presence of strong stimuli, the correlations between motion and quiescence were disrupted for several minutes but homeostasis manifested as an overall elevation of the time spent in quiescence. This response to strong stimuli required the function of the DAF-16/FOXO transcription factor in neurons, but not that of NPR-1. Conversely, response to weak stimuli did not require the function of DAF-16/FOXO. These findings suggest that routine homeostatic stabilization of sleep may be distinct from homeostatic compensation following a strong disturbance. DOI: http://dx.doi.org/10.7554/eLife.04380.001 eLife Sciences Publications, Ltd 2014-12-04 /pmc/articles/PMC4273442/ /pubmed/25474127 http://dx.doi.org/10.7554/eLife.04380 Text en © 2014, Nagy et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Nagy, Stanislav Tramm, Nora Sanders, Jarred Iwanir, Shachar Shirley, Ian A Levine, Erel Biron, David Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
title | Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
title_full | Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
title_fullStr | Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
title_full_unstemmed | Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
title_short | Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
title_sort | homeostasis in c. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273442/ https://www.ncbi.nlm.nih.gov/pubmed/25474127 http://dx.doi.org/10.7554/eLife.04380 |
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