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Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration
Zebrafish can regenerate their damaged hearts throughout their lifespan. It is, however, unknown, whether regeneration remains effective when challenged with successive cycles of cardiac damage in the same animals. Here, we assessed ventricular restoration after two, three and six cryoinjuries inter...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360767/ https://www.ncbi.nlm.nih.gov/pubmed/32665622 http://dx.doi.org/10.1038/s41598-020-68200-1 |
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author | Bise, Thomas Sallin, Pauline Pfefferli, Catherine Jaźwińska, Anna |
author_facet | Bise, Thomas Sallin, Pauline Pfefferli, Catherine Jaźwińska, Anna |
author_sort | Bise, Thomas |
collection | PubMed |
description | Zebrafish can regenerate their damaged hearts throughout their lifespan. It is, however, unknown, whether regeneration remains effective when challenged with successive cycles of cardiac damage in the same animals. Here, we assessed ventricular restoration after two, three and six cryoinjuries interspaced by recovery periods. Using transgenic cell-lineage tracing analysis, we demonstrated that the second cryoinjury damages the regenerated area from the preceding injury, validating the experimental approach. We identified that after multiple cryoinjuries, all hearts regrow a thickened myocardium, similarly to hearts after one cryoinjury. However, the efficiency of scar resorption decreased with the number of repeated cryoinjuries. After six cryoinjuries, all examined hearts failed to completely resolve the fibrotic tissue, demonstrating reduced myocardial restoration. This phenotype was associated with enhanced recruitment of neutrophils and decreased cardiomyocyte proliferation and dedifferentiation at the early regenerative phase. Furthermore, we found that each repeated cryoinjury increased the accumulation of collagen at the injury site. Our analysis demonstrates that the cardiac regenerative program can be successfully activated many times, despite a persisting scar in the wounded area. This finding provides a new perspective for regenerative therapies, aiming in stimulation of organ regeneration in the presence of fibrotic tissue in mammalian models and humans. |
format | Online Article Text |
id | pubmed-7360767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73607672020-07-16 Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration Bise, Thomas Sallin, Pauline Pfefferli, Catherine Jaźwińska, Anna Sci Rep Article Zebrafish can regenerate their damaged hearts throughout their lifespan. It is, however, unknown, whether regeneration remains effective when challenged with successive cycles of cardiac damage in the same animals. Here, we assessed ventricular restoration after two, three and six cryoinjuries interspaced by recovery periods. Using transgenic cell-lineage tracing analysis, we demonstrated that the second cryoinjury damages the regenerated area from the preceding injury, validating the experimental approach. We identified that after multiple cryoinjuries, all hearts regrow a thickened myocardium, similarly to hearts after one cryoinjury. However, the efficiency of scar resorption decreased with the number of repeated cryoinjuries. After six cryoinjuries, all examined hearts failed to completely resolve the fibrotic tissue, demonstrating reduced myocardial restoration. This phenotype was associated with enhanced recruitment of neutrophils and decreased cardiomyocyte proliferation and dedifferentiation at the early regenerative phase. Furthermore, we found that each repeated cryoinjury increased the accumulation of collagen at the injury site. Our analysis demonstrates that the cardiac regenerative program can be successfully activated many times, despite a persisting scar in the wounded area. This finding provides a new perspective for regenerative therapies, aiming in stimulation of organ regeneration in the presence of fibrotic tissue in mammalian models and humans. Nature Publishing Group UK 2020-07-14 /pmc/articles/PMC7360767/ /pubmed/32665622 http://dx.doi.org/10.1038/s41598-020-68200-1 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Bise, Thomas Sallin, Pauline Pfefferli, Catherine Jaźwińska, Anna Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
title | Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
title_full | Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
title_fullStr | Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
title_full_unstemmed | Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
title_short | Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
title_sort | multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360767/ https://www.ncbi.nlm.nih.gov/pubmed/32665622 http://dx.doi.org/10.1038/s41598-020-68200-1 |
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