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Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae
BACKGROUND: Mammals are not able to restore lost appendages, while many amphibians are. One important question about epimorphic regeneration is related to the origin of the new tissues and whether they come from mature cells via dedifferentiation and/or from stem cells. Several studies in urodele am...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313851/ https://www.ncbi.nlm.nih.gov/pubmed/22369050 http://dx.doi.org/10.1186/1471-213X-12-9 |
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author | Rodrigues, Alexandre Miguel Cavaco Christen, Bea Martí, Mercé Izpisúa Belmonte, Juan Carlos |
author_facet | Rodrigues, Alexandre Miguel Cavaco Christen, Bea Martí, Mercé Izpisúa Belmonte, Juan Carlos |
author_sort | Rodrigues, Alexandre Miguel Cavaco |
collection | PubMed |
description | BACKGROUND: Mammals are not able to restore lost appendages, while many amphibians are. One important question about epimorphic regeneration is related to the origin of the new tissues and whether they come from mature cells via dedifferentiation and/or from stem cells. Several studies in urodele amphibians (salamanders) indicate that, after limb or tail amputation, the multinucleated muscle fibres do dedifferentiate by fragmentation and proliferation, thereby contributing to the regenerate. In Xenopus laevis tadpoles, however, it was shown that muscle fibres do not contribute directly to the tail regenerate. We set out to study whether dedifferentiation was present during muscle regeneration of the tadpole limb and zebrafish larval tail, mainly by cell tracing and histological observations. RESULTS: Cell tracing and histological observations indicate that zebrafish tail muscle do not dedifferentiate during regeneration. Technical limitations did not allow us to trace tadpole limb cells, nevertheless we observed no signs of dedifferentiation histologically. However, ultrastructural and gene expression analysis of regenerating muscle in tadpole tail revealed an unexpected dedifferentiation phenotype. Further histological studies showed that dedifferentiating tail fibres did not enter the cell cycle and in vivo cell tracing revealed no evidences of muscle fibre fragmentation. In addition, our results indicate that this incomplete dedifferentiation was initiated by the retraction of muscle fibres. CONCLUSIONS: Our results show that complete skeletal muscle dedifferentiation is less common than expected in lower vertebrates. In addition, the discovery of incomplete dedifferentiation in muscle fibres of the tadpole tail stresses the importance of coupling histological studies with in vivo cell tracing experiments to better understand the regenerative mechanisms. |
format | Online Article Text |
id | pubmed-3313851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33138512012-03-28 Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae Rodrigues, Alexandre Miguel Cavaco Christen, Bea Martí, Mercé Izpisúa Belmonte, Juan Carlos BMC Dev Biol Research Article BACKGROUND: Mammals are not able to restore lost appendages, while many amphibians are. One important question about epimorphic regeneration is related to the origin of the new tissues and whether they come from mature cells via dedifferentiation and/or from stem cells. Several studies in urodele amphibians (salamanders) indicate that, after limb or tail amputation, the multinucleated muscle fibres do dedifferentiate by fragmentation and proliferation, thereby contributing to the regenerate. In Xenopus laevis tadpoles, however, it was shown that muscle fibres do not contribute directly to the tail regenerate. We set out to study whether dedifferentiation was present during muscle regeneration of the tadpole limb and zebrafish larval tail, mainly by cell tracing and histological observations. RESULTS: Cell tracing and histological observations indicate that zebrafish tail muscle do not dedifferentiate during regeneration. Technical limitations did not allow us to trace tadpole limb cells, nevertheless we observed no signs of dedifferentiation histologically. However, ultrastructural and gene expression analysis of regenerating muscle in tadpole tail revealed an unexpected dedifferentiation phenotype. Further histological studies showed that dedifferentiating tail fibres did not enter the cell cycle and in vivo cell tracing revealed no evidences of muscle fibre fragmentation. In addition, our results indicate that this incomplete dedifferentiation was initiated by the retraction of muscle fibres. CONCLUSIONS: Our results show that complete skeletal muscle dedifferentiation is less common than expected in lower vertebrates. In addition, the discovery of incomplete dedifferentiation in muscle fibres of the tadpole tail stresses the importance of coupling histological studies with in vivo cell tracing experiments to better understand the regenerative mechanisms. BioMed Central 2012-02-27 /pmc/articles/PMC3313851/ /pubmed/22369050 http://dx.doi.org/10.1186/1471-213X-12-9 Text en Copyright ©2012 Cavaco Rodrigues et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rodrigues, Alexandre Miguel Cavaco Christen, Bea Martí, Mercé Izpisúa Belmonte, Juan Carlos Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae |
title | Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae |
title_full | Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae |
title_fullStr | Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae |
title_full_unstemmed | Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae |
title_short | Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae |
title_sort | skeletal muscle regeneration in xenopus tadpoles and zebrafish larvae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313851/ https://www.ncbi.nlm.nih.gov/pubmed/22369050 http://dx.doi.org/10.1186/1471-213X-12-9 |
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