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A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress
An animal’s behavioral and physiological response to stressors includes changes to its responses to stimuli. How such changes occur is not well understood. Here we describe a Caenorhabditis elegans quiescent behavior, post-response quiescence (PRQ), which is modulated by the C. elegans response to c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057961/ https://www.ncbi.nlm.nih.gov/pubmed/32139752 http://dx.doi.org/10.1038/s41598-020-60994-4 |
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author | McClanahan, Patrick D. Dubuque, Jessica M. Kontogiorgos-Heintz, Daphne Habermeyer, Ben F. Xu, Joyce H. Ma, Anthony M. Raizen, David M. Fang-Yen, Christopher |
author_facet | McClanahan, Patrick D. Dubuque, Jessica M. Kontogiorgos-Heintz, Daphne Habermeyer, Ben F. Xu, Joyce H. Ma, Anthony M. Raizen, David M. Fang-Yen, Christopher |
author_sort | McClanahan, Patrick D. |
collection | PubMed |
description | An animal’s behavioral and physiological response to stressors includes changes to its responses to stimuli. How such changes occur is not well understood. Here we describe a Caenorhabditis elegans quiescent behavior, post-response quiescence (PRQ), which is modulated by the C. elegans response to cellular stressors. Following an aversive mechanical or blue light stimulus, worms respond first by briefly moving, and then become more quiescent for a period lasting tens of seconds. PRQ occurs at low frequency in unstressed animals, but is more frequent in animals that have experienced cellular stress due to ultraviolet light exposure as well as in animals following overexpression of epidermal growth factor (EGF). PRQ requires the function of the carboxypeptidase EGL-21 and the calcium-activated protein for secretion (CAPS) UNC-31, suggesting it has a neuropeptidergic mechanism. Although PRQ requires the sleep-promoting neurons RIS and ALA, it is not accompanied by decreased arousability, and does not appear to be homeostatically regulated, suggesting that it is not a sleep state. PRQ represents a simple, tractable model for studying how neuromodulatory states like stress alter behavioral responses to stimuli. |
format | Online Article Text |
id | pubmed-7057961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70579612020-03-12 A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress McClanahan, Patrick D. Dubuque, Jessica M. Kontogiorgos-Heintz, Daphne Habermeyer, Ben F. Xu, Joyce H. Ma, Anthony M. Raizen, David M. Fang-Yen, Christopher Sci Rep Article An animal’s behavioral and physiological response to stressors includes changes to its responses to stimuli. How such changes occur is not well understood. Here we describe a Caenorhabditis elegans quiescent behavior, post-response quiescence (PRQ), which is modulated by the C. elegans response to cellular stressors. Following an aversive mechanical or blue light stimulus, worms respond first by briefly moving, and then become more quiescent for a period lasting tens of seconds. PRQ occurs at low frequency in unstressed animals, but is more frequent in animals that have experienced cellular stress due to ultraviolet light exposure as well as in animals following overexpression of epidermal growth factor (EGF). PRQ requires the function of the carboxypeptidase EGL-21 and the calcium-activated protein for secretion (CAPS) UNC-31, suggesting it has a neuropeptidergic mechanism. Although PRQ requires the sleep-promoting neurons RIS and ALA, it is not accompanied by decreased arousability, and does not appear to be homeostatically regulated, suggesting that it is not a sleep state. PRQ represents a simple, tractable model for studying how neuromodulatory states like stress alter behavioral responses to stimuli. Nature Publishing Group UK 2020-03-05 /pmc/articles/PMC7057961/ /pubmed/32139752 http://dx.doi.org/10.1038/s41598-020-60994-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article McClanahan, Patrick D. Dubuque, Jessica M. Kontogiorgos-Heintz, Daphne Habermeyer, Ben F. Xu, Joyce H. Ma, Anthony M. Raizen, David M. Fang-Yen, Christopher A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
title | A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
title_full | A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
title_fullStr | A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
title_full_unstemmed | A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
title_short | A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
title_sort | quiescent state following mild sensory arousal in caenorhabditis elegans is potentiated by stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057961/ https://www.ncbi.nlm.nih.gov/pubmed/32139752 http://dx.doi.org/10.1038/s41598-020-60994-4 |
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