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Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail

Environmental oxidative stress threatens cellular integrity and should therefore be avoided by living organisms. Yet, relatively little is known about environmental oxidative stress perception. Here, using microfluidics, we showed that like I2 pharyngeal neurons, the tail phasmid PHA neurons functio...

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Detalles Bibliográficos
Autores principales: Quintin, Sophie, Aspert, Théo, Ye, Tao, Charvin, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521893/
https://www.ncbi.nlm.nih.gov/pubmed/36173997
http://dx.doi.org/10.1371/journal.pone.0274226
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author Quintin, Sophie
Aspert, Théo
Ye, Tao
Charvin, Gilles
author_facet Quintin, Sophie
Aspert, Théo
Ye, Tao
Charvin, Gilles
author_sort Quintin, Sophie
collection PubMed
description Environmental oxidative stress threatens cellular integrity and should therefore be avoided by living organisms. Yet, relatively little is known about environmental oxidative stress perception. Here, using microfluidics, we showed that like I2 pharyngeal neurons, the tail phasmid PHA neurons function as oxidative stress sensing neurons in C. elegans, but display different responses to H(2)O(2) and light. We uncovered that different but related receptors, GUR-3 and LITE-1, mediate H(2)O(2) signaling in I2 and PHA neurons. Still, the peroxiredoxin PRDX-2 is essential for both, and might promote H(2)O(2)-mediated receptor activation. Our work demonstrates that C. elegans can sense a broad range of oxidative stressors using partially distinct H(2)O(2) signaling pathways in head and tail sensillae, and paves the way for further understanding of how the integration of these inputs translates into the appropriate behavior.
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spelling pubmed-95218932022-09-30 Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail Quintin, Sophie Aspert, Théo Ye, Tao Charvin, Gilles PLoS One Research Article Environmental oxidative stress threatens cellular integrity and should therefore be avoided by living organisms. Yet, relatively little is known about environmental oxidative stress perception. Here, using microfluidics, we showed that like I2 pharyngeal neurons, the tail phasmid PHA neurons function as oxidative stress sensing neurons in C. elegans, but display different responses to H(2)O(2) and light. We uncovered that different but related receptors, GUR-3 and LITE-1, mediate H(2)O(2) signaling in I2 and PHA neurons. Still, the peroxiredoxin PRDX-2 is essential for both, and might promote H(2)O(2)-mediated receptor activation. Our work demonstrates that C. elegans can sense a broad range of oxidative stressors using partially distinct H(2)O(2) signaling pathways in head and tail sensillae, and paves the way for further understanding of how the integration of these inputs translates into the appropriate behavior. Public Library of Science 2022-09-29 /pmc/articles/PMC9521893/ /pubmed/36173997 http://dx.doi.org/10.1371/journal.pone.0274226 Text en © 2022 Quintin et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Quintin, Sophie
Aspert, Théo
Ye, Tao
Charvin, Gilles
Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail
title Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail
title_full Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail
title_fullStr Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail
title_full_unstemmed Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail
title_short Distinct mechanisms underlie H(2)O(2) sensing in C. elegans head and tail
title_sort distinct mechanisms underlie h(2)o(2) sensing in c. elegans head and tail
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521893/
https://www.ncbi.nlm.nih.gov/pubmed/36173997
http://dx.doi.org/10.1371/journal.pone.0274226
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