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An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans
Sensitization is a simple form of behavioral plasticity by which an initial stimulus, often signaling danger, leads to increased responsiveness to subsequent stimuli. Cross-modal sensitization is an important feature of arousal in many organisms, yet its molecular and neural mechanisms are incomplet...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162336/ https://www.ncbi.nlm.nih.gov/pubmed/30146306 http://dx.doi.org/10.1016/j.neuron.2018.08.003 |
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author | Chew, Yee Lian Tanizawa, Yoshinori Cho, Yongmin Zhao, Buyun Yu, Alex J. Ardiel, Evan L. Rabinowitch, Ithai Bai, Jihong Rankin, Catharine H. Lu, Hang Beets, Isabel Schafer, William R. |
author_facet | Chew, Yee Lian Tanizawa, Yoshinori Cho, Yongmin Zhao, Buyun Yu, Alex J. Ardiel, Evan L. Rabinowitch, Ithai Bai, Jihong Rankin, Catharine H. Lu, Hang Beets, Isabel Schafer, William R. |
author_sort | Chew, Yee Lian |
collection | PubMed |
description | Sensitization is a simple form of behavioral plasticity by which an initial stimulus, often signaling danger, leads to increased responsiveness to subsequent stimuli. Cross-modal sensitization is an important feature of arousal in many organisms, yet its molecular and neural mechanisms are incompletely understood. Here we show that in C. elegans, aversive mechanical stimuli lead to both enhanced locomotor activity and sensitization of aversive chemosensory pathways. Both locomotor arousal and cross-modal sensitization depend on the release of FLP-20 neuropeptides from primary mechanosensory neurons and on their receptor FRPR-3. Surprisingly, the critical site of action of FRPR-3 for both sensory and locomotor arousal is RID, a single neuroendocrine cell specialized for the release of neuropeptides that responds to mechanical stimuli in a FLP-20-dependent manner. Thus, FLP-20 peptides function as an afferent arousal signal that conveys mechanosensory information to central neurons that modulate arousal and other behavioral states. VIDEO ABSTRACT: |
format | Online Article Text |
id | pubmed-6162336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61623362018-10-01 An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans Chew, Yee Lian Tanizawa, Yoshinori Cho, Yongmin Zhao, Buyun Yu, Alex J. Ardiel, Evan L. Rabinowitch, Ithai Bai, Jihong Rankin, Catharine H. Lu, Hang Beets, Isabel Schafer, William R. Neuron Article Sensitization is a simple form of behavioral plasticity by which an initial stimulus, often signaling danger, leads to increased responsiveness to subsequent stimuli. Cross-modal sensitization is an important feature of arousal in many organisms, yet its molecular and neural mechanisms are incompletely understood. Here we show that in C. elegans, aversive mechanical stimuli lead to both enhanced locomotor activity and sensitization of aversive chemosensory pathways. Both locomotor arousal and cross-modal sensitization depend on the release of FLP-20 neuropeptides from primary mechanosensory neurons and on their receptor FRPR-3. Surprisingly, the critical site of action of FRPR-3 for both sensory and locomotor arousal is RID, a single neuroendocrine cell specialized for the release of neuropeptides that responds to mechanical stimuli in a FLP-20-dependent manner. Thus, FLP-20 peptides function as an afferent arousal signal that conveys mechanosensory information to central neurons that modulate arousal and other behavioral states. VIDEO ABSTRACT: Cell Press 2018-09-19 /pmc/articles/PMC6162336/ /pubmed/30146306 http://dx.doi.org/10.1016/j.neuron.2018.08.003 Text en © 2018 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chew, Yee Lian Tanizawa, Yoshinori Cho, Yongmin Zhao, Buyun Yu, Alex J. Ardiel, Evan L. Rabinowitch, Ithai Bai, Jihong Rankin, Catharine H. Lu, Hang Beets, Isabel Schafer, William R. An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans |
title | An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans |
title_full | An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans |
title_fullStr | An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans |
title_full_unstemmed | An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans |
title_short | An Afferent Neuropeptide System Transmits Mechanosensory Signals Triggering Sensitization and Arousal in C. elegans |
title_sort | afferent neuropeptide system transmits mechanosensory signals triggering sensitization and arousal in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162336/ https://www.ncbi.nlm.nih.gov/pubmed/30146306 http://dx.doi.org/10.1016/j.neuron.2018.08.003 |
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