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Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals
Why mammals have poor regenerative ability has remained a long-standing question in biology. In regenerating vertebrates, injury can induce a process known as epimorphic regeneration to replace damaged structures. Using a 4-mm ear punch assay across multiple mammalian species, here we show that seve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848467/ https://www.ncbi.nlm.nih.gov/pubmed/27109826 http://dx.doi.org/10.1038/ncomms11164 |
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author | Gawriluk, Thomas R. Simkin, Jennifer Thompson, Katherine L. Biswas, Shishir K. Clare-Salzler, Zak Kimani, John M. Kiama, Stephen G. Smith, Jeramiah J. Ezenwa, Vanessa O. Seifert, Ashley W. |
author_facet | Gawriluk, Thomas R. Simkin, Jennifer Thompson, Katherine L. Biswas, Shishir K. Clare-Salzler, Zak Kimani, John M. Kiama, Stephen G. Smith, Jeramiah J. Ezenwa, Vanessa O. Seifert, Ashley W. |
author_sort | Gawriluk, Thomas R. |
collection | PubMed |
description | Why mammals have poor regenerative ability has remained a long-standing question in biology. In regenerating vertebrates, injury can induce a process known as epimorphic regeneration to replace damaged structures. Using a 4-mm ear punch assay across multiple mammalian species, here we show that several Acomys spp. (spiny mice) and Oryctolagus cuniculus completely regenerate tissue, whereas other rodents including MRL/MpJ ‘healer' mice heal similar injuries by scarring. We demonstrate ear-hole closure is independent of ear size, and closure rate can be modelled with a cubic function. Cellular and genetic analyses reveal that injury induces blastema formation in Acomys cahirinus. Despite cell cycle re-entry in Mus musculus and A. cahirinus, efficient cell cycle progression and proliferation only occurs in spiny mice. Together, our data unite blastema-mediated regeneration in spiny mice with regeneration in other vertebrates such as salamanders, newts and zebrafish, where all healthy adults regenerate in response to injury. |
format | Online Article Text |
id | pubmed-4848467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48484672016-05-05 Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals Gawriluk, Thomas R. Simkin, Jennifer Thompson, Katherine L. Biswas, Shishir K. Clare-Salzler, Zak Kimani, John M. Kiama, Stephen G. Smith, Jeramiah J. Ezenwa, Vanessa O. Seifert, Ashley W. Nat Commun Article Why mammals have poor regenerative ability has remained a long-standing question in biology. In regenerating vertebrates, injury can induce a process known as epimorphic regeneration to replace damaged structures. Using a 4-mm ear punch assay across multiple mammalian species, here we show that several Acomys spp. (spiny mice) and Oryctolagus cuniculus completely regenerate tissue, whereas other rodents including MRL/MpJ ‘healer' mice heal similar injuries by scarring. We demonstrate ear-hole closure is independent of ear size, and closure rate can be modelled with a cubic function. Cellular and genetic analyses reveal that injury induces blastema formation in Acomys cahirinus. Despite cell cycle re-entry in Mus musculus and A. cahirinus, efficient cell cycle progression and proliferation only occurs in spiny mice. Together, our data unite blastema-mediated regeneration in spiny mice with regeneration in other vertebrates such as salamanders, newts and zebrafish, where all healthy adults regenerate in response to injury. Nature Publishing Group 2016-04-25 /pmc/articles/PMC4848467/ /pubmed/27109826 http://dx.doi.org/10.1038/ncomms11164 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gawriluk, Thomas R. Simkin, Jennifer Thompson, Katherine L. Biswas, Shishir K. Clare-Salzler, Zak Kimani, John M. Kiama, Stephen G. Smith, Jeramiah J. Ezenwa, Vanessa O. Seifert, Ashley W. Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
title | Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
title_full | Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
title_fullStr | Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
title_full_unstemmed | Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
title_short | Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
title_sort | comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848467/ https://www.ncbi.nlm.nih.gov/pubmed/27109826 http://dx.doi.org/10.1038/ncomms11164 |
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