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Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity
While most tetrapods are unable to regenerate severed body parts, amphibians display a remarkable ability to regenerate an array of structures. Frogs can regenerate appendages as larva, but they lose this ability around metamorphosis. In contrast, salamanders regenerate appendages as larva, juvenile...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895291/ https://www.ncbi.nlm.nih.gov/pubmed/27499857 http://dx.doi.org/10.1002/reg2.8 |
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author | Monaghan, James R. Stier, Adrian C. Michonneau, François Smith, Matthew D. Pasch, Bret Maden, Malcolm Seifert, Ashley W. |
author_facet | Monaghan, James R. Stier, Adrian C. Michonneau, François Smith, Matthew D. Pasch, Bret Maden, Malcolm Seifert, Ashley W. |
author_sort | Monaghan, James R. |
collection | PubMed |
description | While most tetrapods are unable to regenerate severed body parts, amphibians display a remarkable ability to regenerate an array of structures. Frogs can regenerate appendages as larva, but they lose this ability around metamorphosis. In contrast, salamanders regenerate appendages as larva, juveniles, and adults. However, the extent to which fundamental traits (e.g., metamorphosis, body size, aging, etc.) restrict regenerative ability remains contentious. Here we utilize the ability of normally paedomorphic adult axolotls (Ambystoma mexicanum) to undergo induced metamorphosis by thyroxine exposure to test how metamorphosis and body size affects regeneration in age‐matched paedomorphic and metamorphic individuals. We show that body size does not affect regeneration in adult axolotls, but metamorphosis causes a twofold reduction in regeneration rate, and lead to carpal and digit malformations. Furthermore, we find evidence that metamorphic blastemal cells may take longer to traverse the cell cycle and display a lower proliferative rate. This study identifies the axolotl as a powerful system to study how metamorphosis restricts regeneration independently of developmental stage, body size, and age; and more broadly how metamorphosis affects tissue‐specific changes. |
format | Online Article Text |
id | pubmed-4895291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48952912016-08-05 Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity Monaghan, James R. Stier, Adrian C. Michonneau, François Smith, Matthew D. Pasch, Bret Maden, Malcolm Seifert, Ashley W. Regeneration (Oxf) Research Articles While most tetrapods are unable to regenerate severed body parts, amphibians display a remarkable ability to regenerate an array of structures. Frogs can regenerate appendages as larva, but they lose this ability around metamorphosis. In contrast, salamanders regenerate appendages as larva, juveniles, and adults. However, the extent to which fundamental traits (e.g., metamorphosis, body size, aging, etc.) restrict regenerative ability remains contentious. Here we utilize the ability of normally paedomorphic adult axolotls (Ambystoma mexicanum) to undergo induced metamorphosis by thyroxine exposure to test how metamorphosis and body size affects regeneration in age‐matched paedomorphic and metamorphic individuals. We show that body size does not affect regeneration in adult axolotls, but metamorphosis causes a twofold reduction in regeneration rate, and lead to carpal and digit malformations. Furthermore, we find evidence that metamorphic blastemal cells may take longer to traverse the cell cycle and display a lower proliferative rate. This study identifies the axolotl as a powerful system to study how metamorphosis restricts regeneration independently of developmental stage, body size, and age; and more broadly how metamorphosis affects tissue‐specific changes. John Wiley and Sons Inc. 2014-02-20 /pmc/articles/PMC4895291/ /pubmed/27499857 http://dx.doi.org/10.1002/reg2.8 Text en © 2014 The Authors. Regeneration published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Monaghan, James R. Stier, Adrian C. Michonneau, François Smith, Matthew D. Pasch, Bret Maden, Malcolm Seifert, Ashley W. Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
title | Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
title_full | Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
title_fullStr | Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
title_full_unstemmed | Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
title_short | Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
title_sort | experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895291/ https://www.ncbi.nlm.nih.gov/pubmed/27499857 http://dx.doi.org/10.1002/reg2.8 |
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