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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...
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/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. |
format | Online Article Text |
id | pubmed-7176127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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