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Active Notch signaling is required for arm regeneration in a brittle star

Cell signaling pathways play key roles in coordinating cellular events in development. The Notch signaling pathway is highly conserved across all multicellular animals and is known to coordinate a multitude of diverse cellular events, including proliferation, differentiation, fate specification, and...

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Autores principales: Mashanov, Vladimir, Akiona, Jennifer, Khoury, Maleana, Ferrier, Jacob, Reid, Robert, Machado, Denis Jacob, Zueva, Olga, Janies, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217437/
https://www.ncbi.nlm.nih.gov/pubmed/32396580
http://dx.doi.org/10.1371/journal.pone.0232981
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author Mashanov, Vladimir
Akiona, Jennifer
Khoury, Maleana
Ferrier, Jacob
Reid, Robert
Machado, Denis Jacob
Zueva, Olga
Janies, Daniel
author_facet Mashanov, Vladimir
Akiona, Jennifer
Khoury, Maleana
Ferrier, Jacob
Reid, Robert
Machado, Denis Jacob
Zueva, Olga
Janies, Daniel
author_sort Mashanov, Vladimir
collection PubMed
description Cell signaling pathways play key roles in coordinating cellular events in development. The Notch signaling pathway is highly conserved across all multicellular animals and is known to coordinate a multitude of diverse cellular events, including proliferation, differentiation, fate specification, and cell death. Specific functions of the pathway are, however, highly context-dependent and are not well characterized in post-traumatic regeneration. Here, we use a small-molecule inhibitor of the pathway (DAPT) to demonstrate that Notch signaling is required for proper arm regeneration in the brittle star Ophioderma brevispina, a highly regenerative member of the phylum Echinodermata. We also employ a transcriptome-wide gene expression analysis (RNA-seq) to characterize the downstream genes controlled by the Notch pathway in the brittle star regeneration. We demonstrate that arm regeneration involves an extensive cross-talk between the Notch pathway and other cell signaling pathways. In the regrowing arm, Notch regulates the composition of the extracellular matrix, cell migration, proliferation, and apoptosis, as well as components of the innate immune response. We also show for the first time that Notch signaling regulates the activity of several transposable elements. Our data also suggests that one of the possible mechanisms through which Notch sustains its activity in the regenerating tissues is via suppression of Neuralized1.
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spelling pubmed-72174372020-05-26 Active Notch signaling is required for arm regeneration in a brittle star Mashanov, Vladimir Akiona, Jennifer Khoury, Maleana Ferrier, Jacob Reid, Robert Machado, Denis Jacob Zueva, Olga Janies, Daniel PLoS One Research Article Cell signaling pathways play key roles in coordinating cellular events in development. The Notch signaling pathway is highly conserved across all multicellular animals and is known to coordinate a multitude of diverse cellular events, including proliferation, differentiation, fate specification, and cell death. Specific functions of the pathway are, however, highly context-dependent and are not well characterized in post-traumatic regeneration. Here, we use a small-molecule inhibitor of the pathway (DAPT) to demonstrate that Notch signaling is required for proper arm regeneration in the brittle star Ophioderma brevispina, a highly regenerative member of the phylum Echinodermata. We also employ a transcriptome-wide gene expression analysis (RNA-seq) to characterize the downstream genes controlled by the Notch pathway in the brittle star regeneration. We demonstrate that arm regeneration involves an extensive cross-talk between the Notch pathway and other cell signaling pathways. In the regrowing arm, Notch regulates the composition of the extracellular matrix, cell migration, proliferation, and apoptosis, as well as components of the innate immune response. We also show for the first time that Notch signaling regulates the activity of several transposable elements. Our data also suggests that one of the possible mechanisms through which Notch sustains its activity in the regenerating tissues is via suppression of Neuralized1. Public Library of Science 2020-05-12 /pmc/articles/PMC7217437/ /pubmed/32396580 http://dx.doi.org/10.1371/journal.pone.0232981 Text en © 2020 Mashanov et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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
Mashanov, Vladimir
Akiona, Jennifer
Khoury, Maleana
Ferrier, Jacob
Reid, Robert
Machado, Denis Jacob
Zueva, Olga
Janies, Daniel
Active Notch signaling is required for arm regeneration in a brittle star
title Active Notch signaling is required for arm regeneration in a brittle star
title_full Active Notch signaling is required for arm regeneration in a brittle star
title_fullStr Active Notch signaling is required for arm regeneration in a brittle star
title_full_unstemmed Active Notch signaling is required for arm regeneration in a brittle star
title_short Active Notch signaling is required for arm regeneration in a brittle star
title_sort active notch signaling is required for arm regeneration in a brittle star
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217437/
https://www.ncbi.nlm.nih.gov/pubmed/32396580
http://dx.doi.org/10.1371/journal.pone.0232981
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