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Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish

Severely damaged adult zebrafish extraocular muscles (EOMs) regenerate through dedifferentiation of residual myocytes involving a muscle-to-mesenchyme transition. Members of the Twist family of basic helix-loop-helix transcription factors (TFs) are key regulators of the epithelial-mesenchymal transi...

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Autores principales: Zhao, Yi, Louie, Ke’ale W., Tingle, Christina F., Sha, Cuilee, Heisel, Curtis J., Unsworth, Shelby P., Kish, Phillip E., Kahana, Alon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176127/
https://www.ncbi.nlm.nih.gov/pubmed/32320444
http://dx.doi.org/10.1371/journal.pone.0231963
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author Zhao, Yi
Louie, Ke’ale W.
Tingle, Christina F.
Sha, Cuilee
Heisel, Curtis J.
Unsworth, Shelby P.
Kish, Phillip E.
Kahana, Alon
author_facet Zhao, Yi
Louie, Ke’ale W.
Tingle, Christina F.
Sha, Cuilee
Heisel, Curtis J.
Unsworth, Shelby P.
Kish, Phillip E.
Kahana, Alon
author_sort Zhao, Yi
collection PubMed
description Severely damaged adult zebrafish extraocular muscles (EOMs) regenerate through dedifferentiation of residual myocytes involving a muscle-to-mesenchyme transition. Members of the Twist family of basic helix-loop-helix transcription factors (TFs) are key regulators of the epithelial-mesenchymal transition (EMT) and are also involved in craniofacial development in humans and animal models. During zebrafish embryogenesis, twist family members (twist1a, twist1b, twist2, and twist3) function to regulate craniofacial skeletal development. Because of their roles as master regulators of stem cell biology, we hypothesized that twist TFs regulate adult EOM repair and regeneration. In this study, utilizing an adult zebrafish EOM regeneration model, we demonstrate that inhibiting twist3 function using translation-blocking morpholino oligonucleotides (MOs) impairs muscle regeneration by reducing myocyte dedifferentiation and proliferation in the regenerating muscle. This supports our hypothesis that twist TFs are involved in the early steps of dedifferentiation and highlights the importance of twist3 during EOM regeneration.
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spelling pubmed-71761272020-05-12 Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish Zhao, Yi Louie, Ke’ale W. Tingle, Christina F. Sha, Cuilee Heisel, Curtis J. Unsworth, Shelby P. Kish, Phillip E. Kahana, Alon PLoS One Research Article Severely damaged adult zebrafish extraocular muscles (EOMs) regenerate through dedifferentiation of residual myocytes involving a muscle-to-mesenchyme transition. Members of the Twist family of basic helix-loop-helix transcription factors (TFs) are key regulators of the epithelial-mesenchymal transition (EMT) and are also involved in craniofacial development in humans and animal models. During zebrafish embryogenesis, twist family members (twist1a, twist1b, twist2, and twist3) function to regulate craniofacial skeletal development. Because of their roles as master regulators of stem cell biology, we hypothesized that twist TFs regulate adult EOM repair and regeneration. In this study, utilizing an adult zebrafish EOM regeneration model, we demonstrate that inhibiting twist3 function using translation-blocking morpholino oligonucleotides (MOs) impairs muscle regeneration by reducing myocyte dedifferentiation and proliferation in the regenerating muscle. This supports our hypothesis that twist TFs are involved in the early steps of dedifferentiation and highlights the importance of twist3 during EOM regeneration. Public Library of Science 2020-04-22 /pmc/articles/PMC7176127/ /pubmed/32320444 http://dx.doi.org/10.1371/journal.pone.0231963 Text en © 2020 Zhao 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
Zhao, Yi
Louie, Ke’ale W.
Tingle, Christina F.
Sha, Cuilee
Heisel, Curtis J.
Unsworth, Shelby P.
Kish, Phillip E.
Kahana, Alon
Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
title Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
title_full Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
title_fullStr Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
title_full_unstemmed Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
title_short Twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
title_sort twist3 is required for dedifferentiation during extraocular muscle regeneration in adult zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176127/
https://www.ncbi.nlm.nih.gov/pubmed/32320444
http://dx.doi.org/10.1371/journal.pone.0231963
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