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Model organisms at the heart of regeneration

Heart failure is a major cause of death worldwide owing to the inability of the adult human heart to regenerate after a heart attack. However, many vertebrate species are capable of complete cardiac regeneration following injury. In this Review, we discuss the various model organisms of cardiac rege...

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Detalles Bibliográficos
Autores principales: Price, Eleanor L., Vieira, Joaquim M., Riley, Paul R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826025/
https://www.ncbi.nlm.nih.gov/pubmed/31562250
http://dx.doi.org/10.1242/dmm.040691
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author Price, Eleanor L.
Vieira, Joaquim M.
Riley, Paul R.
author_facet Price, Eleanor L.
Vieira, Joaquim M.
Riley, Paul R.
author_sort Price, Eleanor L.
collection PubMed
description Heart failure is a major cause of death worldwide owing to the inability of the adult human heart to regenerate after a heart attack. However, many vertebrate species are capable of complete cardiac regeneration following injury. In this Review, we discuss the various model organisms of cardiac regeneration, and outline what they have taught us thus far about the cellular and molecular responses essential for optimal cardiac repair. We compare across different species, highlighting evolutionarily conserved mechanisms of regeneration and demonstrating the importance of developmental gene expression programmes, plasticity of the heart and the pathophysiological environment for the regenerative response. Additionally, we discuss how the findings from these studies have led to improvements in cardiac repair in preclinical models such as adult mice and pigs, and discuss the potential to translate these findings into therapeutic approaches for human patients following myocardial infarction.
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spelling pubmed-68260252019-11-04 Model organisms at the heart of regeneration Price, Eleanor L. Vieira, Joaquim M. Riley, Paul R. Dis Model Mech Review Heart failure is a major cause of death worldwide owing to the inability of the adult human heart to regenerate after a heart attack. However, many vertebrate species are capable of complete cardiac regeneration following injury. In this Review, we discuss the various model organisms of cardiac regeneration, and outline what they have taught us thus far about the cellular and molecular responses essential for optimal cardiac repair. We compare across different species, highlighting evolutionarily conserved mechanisms of regeneration and demonstrating the importance of developmental gene expression programmes, plasticity of the heart and the pathophysiological environment for the regenerative response. Additionally, we discuss how the findings from these studies have led to improvements in cardiac repair in preclinical models such as adult mice and pigs, and discuss the potential to translate these findings into therapeutic approaches for human patients following myocardial infarction. The Company of Biologists Ltd 2019-10-01 2019-09-27 /pmc/articles/PMC6826025/ /pubmed/31562250 http://dx.doi.org/10.1242/dmm.040691 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Review
Price, Eleanor L.
Vieira, Joaquim M.
Riley, Paul R.
Model organisms at the heart of regeneration
title Model organisms at the heart of regeneration
title_full Model organisms at the heart of regeneration
title_fullStr Model organisms at the heart of regeneration
title_full_unstemmed Model organisms at the heart of regeneration
title_short Model organisms at the heart of regeneration
title_sort model organisms at the heart of regeneration
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826025/
https://www.ncbi.nlm.nih.gov/pubmed/31562250
http://dx.doi.org/10.1242/dmm.040691
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