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Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish

Zebrafish have the ability to regenerate damaged cells and tissues by activating quiescent stem and progenitor cells or reprogramming differentiated cells into regeneration-competent precursors. Proliferation among the cells that will functionally restore injured tissues is a fundamental biological...

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Autores principales: Ang, Nicholas B., Saera-Vila, Alfonso, Walsh, Caroline, Hitchcock, Peter F., Kahana, Alon, Thummel, Ryan, Nagashima, Mikiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292404/
https://www.ncbi.nlm.nih.gov/pubmed/32530962
http://dx.doi.org/10.1371/journal.pone.0232308
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author Ang, Nicholas B.
Saera-Vila, Alfonso
Walsh, Caroline
Hitchcock, Peter F.
Kahana, Alon
Thummel, Ryan
Nagashima, Mikiko
author_facet Ang, Nicholas B.
Saera-Vila, Alfonso
Walsh, Caroline
Hitchcock, Peter F.
Kahana, Alon
Thummel, Ryan
Nagashima, Mikiko
author_sort Ang, Nicholas B.
collection PubMed
description Zebrafish have the ability to regenerate damaged cells and tissues by activating quiescent stem and progenitor cells or reprogramming differentiated cells into regeneration-competent precursors. Proliferation among the cells that will functionally restore injured tissues is a fundamental biological process underlying regeneration. Midkine-a is a cytokine growth factor, whose expression is strongly induced by injury in a variety of tissues across a range of vertebrate classes. Using a zebrafish Midkine-a loss of function mutant, we evaluated regeneration of caudal fin, extraocular muscle and retinal neurons to investigate the function of Midkine-a during epimorphic regeneration. In wildtype zebrafish, injury among these tissues induces robust proliferation and rapid regeneration. In Midkine-a mutants, the initial proliferation in each of these tissues is significantly diminished or absent. Regeneration of the caudal fin and extraocular muscle is delayed; regeneration of the retina is nearly completely absent. These data demonstrate that Midkine-a is universally required in the signaling pathways that convert tissue injury into the initial burst of cell proliferation. Further, these data highlight differences in the molecular mechanisms that regulate epimorphic regeneration in zebrafish.
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spelling pubmed-72924042020-06-18 Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish Ang, Nicholas B. Saera-Vila, Alfonso Walsh, Caroline Hitchcock, Peter F. Kahana, Alon Thummel, Ryan Nagashima, Mikiko PLoS One Research Article Zebrafish have the ability to regenerate damaged cells and tissues by activating quiescent stem and progenitor cells or reprogramming differentiated cells into regeneration-competent precursors. Proliferation among the cells that will functionally restore injured tissues is a fundamental biological process underlying regeneration. Midkine-a is a cytokine growth factor, whose expression is strongly induced by injury in a variety of tissues across a range of vertebrate classes. Using a zebrafish Midkine-a loss of function mutant, we evaluated regeneration of caudal fin, extraocular muscle and retinal neurons to investigate the function of Midkine-a during epimorphic regeneration. In wildtype zebrafish, injury among these tissues induces robust proliferation and rapid regeneration. In Midkine-a mutants, the initial proliferation in each of these tissues is significantly diminished or absent. Regeneration of the caudal fin and extraocular muscle is delayed; regeneration of the retina is nearly completely absent. These data demonstrate that Midkine-a is universally required in the signaling pathways that convert tissue injury into the initial burst of cell proliferation. Further, these data highlight differences in the molecular mechanisms that regulate epimorphic regeneration in zebrafish. Public Library of Science 2020-06-12 /pmc/articles/PMC7292404/ /pubmed/32530962 http://dx.doi.org/10.1371/journal.pone.0232308 Text en © 2020 Ang 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
Ang, Nicholas B.
Saera-Vila, Alfonso
Walsh, Caroline
Hitchcock, Peter F.
Kahana, Alon
Thummel, Ryan
Nagashima, Mikiko
Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
title Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
title_full Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
title_fullStr Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
title_full_unstemmed Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
title_short Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
title_sort midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292404/
https://www.ncbi.nlm.nih.gov/pubmed/32530962
http://dx.doi.org/10.1371/journal.pone.0232308
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