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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7292404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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