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Ischemic tolerance and cardiac repair in the spiny mouse (Acomys)
Ischemic heart disease and by extension myocardial infarction is the primary cause of death worldwide, warranting regenerative therapies to restore heart function. Current models of natural heart regeneration are restricted in that they are not of adult mammalian origin, precluding the study of clas...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599451/ https://www.ncbi.nlm.nih.gov/pubmed/34789755 http://dx.doi.org/10.1038/s41536-021-00188-2 |
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author | Koopmans, Tim van Beijnum, Henriette Roovers, Elke F. Tomasso, Antonio Malhotra, Divyanshu Boeter, Jochem Psathaki, Olympia E. Versteeg, Danielle van Rooij, Eva Bartscherer, Kerstin |
author_facet | Koopmans, Tim van Beijnum, Henriette Roovers, Elke F. Tomasso, Antonio Malhotra, Divyanshu Boeter, Jochem Psathaki, Olympia E. Versteeg, Danielle van Rooij, Eva Bartscherer, Kerstin |
author_sort | Koopmans, Tim |
collection | PubMed |
description | Ischemic heart disease and by extension myocardial infarction is the primary cause of death worldwide, warranting regenerative therapies to restore heart function. Current models of natural heart regeneration are restricted in that they are not of adult mammalian origin, precluding the study of class-specific traits that have emerged throughout evolution, and reducing translatability of research findings to humans. Here, we present the spiny mouse (Acomys spp.), a murid rodent that exhibits bona fide regeneration of the back skin and ear pinna, as a model to study heart repair. By comparing them to ordinary mice (Mus musculus), we show that the acute injury response in spiny mice is similar, but with an associated tolerance to infarction through superior survivability, improved ventricular conduction, and near-absence of pathological remodeling. Critically, spiny mice display increased vascularization, altered scar organization, and a more immature phenotype of cardiomyocytes, with a corresponding improvement in heart function. These findings present new avenues for mammalian heart research by leveraging unique tissue properties of the spiny mouse. |
format | Online Article Text |
id | pubmed-8599451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85994512021-11-19 Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) Koopmans, Tim van Beijnum, Henriette Roovers, Elke F. Tomasso, Antonio Malhotra, Divyanshu Boeter, Jochem Psathaki, Olympia E. Versteeg, Danielle van Rooij, Eva Bartscherer, Kerstin NPJ Regen Med Article Ischemic heart disease and by extension myocardial infarction is the primary cause of death worldwide, warranting regenerative therapies to restore heart function. Current models of natural heart regeneration are restricted in that they are not of adult mammalian origin, precluding the study of class-specific traits that have emerged throughout evolution, and reducing translatability of research findings to humans. Here, we present the spiny mouse (Acomys spp.), a murid rodent that exhibits bona fide regeneration of the back skin and ear pinna, as a model to study heart repair. By comparing them to ordinary mice (Mus musculus), we show that the acute injury response in spiny mice is similar, but with an associated tolerance to infarction through superior survivability, improved ventricular conduction, and near-absence of pathological remodeling. Critically, spiny mice display increased vascularization, altered scar organization, and a more immature phenotype of cardiomyocytes, with a corresponding improvement in heart function. These findings present new avenues for mammalian heart research by leveraging unique tissue properties of the spiny mouse. Nature Publishing Group UK 2021-11-17 /pmc/articles/PMC8599451/ /pubmed/34789755 http://dx.doi.org/10.1038/s41536-021-00188-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Koopmans, Tim van Beijnum, Henriette Roovers, Elke F. Tomasso, Antonio Malhotra, Divyanshu Boeter, Jochem Psathaki, Olympia E. Versteeg, Danielle van Rooij, Eva Bartscherer, Kerstin Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) |
title | Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) |
title_full | Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) |
title_fullStr | Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) |
title_full_unstemmed | Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) |
title_short | Ischemic tolerance and cardiac repair in the spiny mouse (Acomys) |
title_sort | ischemic tolerance and cardiac repair in the spiny mouse (acomys) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599451/ https://www.ncbi.nlm.nih.gov/pubmed/34789755 http://dx.doi.org/10.1038/s41536-021-00188-2 |
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