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Youth is wasted on the young

Amphibians and zebrafish are able to regenerate lost myocardial tissue without loss of cardiac function; whereas mammals, in response to myocardial injury, develop scar and lose cardiac function. This dichotomy of response has been thought to be due to the fact that adult mammalian cardiac myocytes...

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Detalles Bibliográficos
Autores principales: Penn, Marc S, Mayorga, Martiza E, Dong, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152994/
https://www.ncbi.nlm.nih.gov/pubmed/21596004
http://dx.doi.org/10.1186/scrt65
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author Penn, Marc S
Mayorga, Martiza E
Dong, Feng
author_facet Penn, Marc S
Mayorga, Martiza E
Dong, Feng
author_sort Penn, Marc S
collection PubMed
description Amphibians and zebrafish are able to regenerate lost myocardial tissue without loss of cardiac function; whereas mammals, in response to myocardial injury, develop scar and lose cardiac function. This dichotomy of response has been thought to be due to the fact that adult mammalian cardiac myocytes are multinucleated and have limited proliferative capacity. Neonatal mammalian cardiac myocytes do have a limited capacity to proliferate. What has been unknown is whether this limited proliferative capacity is associated with the ability to regenerate myocardial tissue soon after birth. Recently, it has been demonstrated that 1-day-old neonatal mice do have the ability to regenerate resected cardiac tissue, and that the capacity to regenerate cardiac tissue is lost by 7 days after birth. The present commentary reviews these results and attempts to offer perspective as to how these important findings relate to current and future strategies to prevent and treat cardiac dysfunction in clinical populations.
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spelling pubmed-31529942012-05-18 Youth is wasted on the young Penn, Marc S Mayorga, Martiza E Dong, Feng Stem Cell Res Ther Commentary Amphibians and zebrafish are able to regenerate lost myocardial tissue without loss of cardiac function; whereas mammals, in response to myocardial injury, develop scar and lose cardiac function. This dichotomy of response has been thought to be due to the fact that adult mammalian cardiac myocytes are multinucleated and have limited proliferative capacity. Neonatal mammalian cardiac myocytes do have a limited capacity to proliferate. What has been unknown is whether this limited proliferative capacity is associated with the ability to regenerate myocardial tissue soon after birth. Recently, it has been demonstrated that 1-day-old neonatal mice do have the ability to regenerate resected cardiac tissue, and that the capacity to regenerate cardiac tissue is lost by 7 days after birth. The present commentary reviews these results and attempts to offer perspective as to how these important findings relate to current and future strategies to prevent and treat cardiac dysfunction in clinical populations. BioMed Central 2011-05-18 /pmc/articles/PMC3152994/ /pubmed/21596004 http://dx.doi.org/10.1186/scrt65 Text en Copyright ©2011 BioMed Central Ltd
spellingShingle Commentary
Penn, Marc S
Mayorga, Martiza E
Dong, Feng
Youth is wasted on the young
title Youth is wasted on the young
title_full Youth is wasted on the young
title_fullStr Youth is wasted on the young
title_full_unstemmed Youth is wasted on the young
title_short Youth is wasted on the young
title_sort youth is wasted on the young
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152994/
https://www.ncbi.nlm.nih.gov/pubmed/21596004
http://dx.doi.org/10.1186/scrt65
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