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Clonally dominant cardiomyocytes direct heart morphogenesis

As vertebrate embryos develop to adulthood, their organs dramatically increase size and change tissue architecture. Here, we used a multicolor clonal analysis to define contributions of many individual cardiomyocytes as the zebrafish heart undergoes morphogenesis from a primitive embryonic structure...

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Detalles Bibliográficos
Autores principales: Gupta, Vikas, Poss, Kenneth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340018/
https://www.ncbi.nlm.nih.gov/pubmed/22538609
http://dx.doi.org/10.1038/nature11045
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author Gupta, Vikas
Poss, Kenneth D.
author_facet Gupta, Vikas
Poss, Kenneth D.
author_sort Gupta, Vikas
collection PubMed
description As vertebrate embryos develop to adulthood, their organs dramatically increase size and change tissue architecture. Here, we used a multicolor clonal analysis to define contributions of many individual cardiomyocytes as the zebrafish heart undergoes morphogenesis from a primitive embryonic structure into its complex adult form. We find that the single cardiomyocyte-thick wall of the juvenile ventricle forms by lateral expansion of several dozen cardiomyocytes into muscle patches of variable sizes and shapes. As juveniles mature into adults, this structure becomes fully enveloped by a new lineage of cortical muscle. Adult cortical muscle originates from a small number (~8) of cardiomyocytes that display clonal dominance reminiscent of stem cell populations. Cortical cardiomyocytes initially emerge from internal myofibers that in rare events breach the juvenile ventricular wall and expand over the surface. Our study illuminates dynamic proliferative behaviors that generate adult cardiac structure, revealing clonal dominance as a key mechanism that shapes a vertebrate organ.
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spelling pubmed-33400182012-10-26 Clonally dominant cardiomyocytes direct heart morphogenesis Gupta, Vikas Poss, Kenneth D. Nature Article As vertebrate embryos develop to adulthood, their organs dramatically increase size and change tissue architecture. Here, we used a multicolor clonal analysis to define contributions of many individual cardiomyocytes as the zebrafish heart undergoes morphogenesis from a primitive embryonic structure into its complex adult form. We find that the single cardiomyocyte-thick wall of the juvenile ventricle forms by lateral expansion of several dozen cardiomyocytes into muscle patches of variable sizes and shapes. As juveniles mature into adults, this structure becomes fully enveloped by a new lineage of cortical muscle. Adult cortical muscle originates from a small number (~8) of cardiomyocytes that display clonal dominance reminiscent of stem cell populations. Cortical cardiomyocytes initially emerge from internal myofibers that in rare events breach the juvenile ventricular wall and expand over the surface. Our study illuminates dynamic proliferative behaviors that generate adult cardiac structure, revealing clonal dominance as a key mechanism that shapes a vertebrate organ. 2012-04-25 /pmc/articles/PMC3340018/ /pubmed/22538609 http://dx.doi.org/10.1038/nature11045 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Gupta, Vikas
Poss, Kenneth D.
Clonally dominant cardiomyocytes direct heart morphogenesis
title Clonally dominant cardiomyocytes direct heart morphogenesis
title_full Clonally dominant cardiomyocytes direct heart morphogenesis
title_fullStr Clonally dominant cardiomyocytes direct heart morphogenesis
title_full_unstemmed Clonally dominant cardiomyocytes direct heart morphogenesis
title_short Clonally dominant cardiomyocytes direct heart morphogenesis
title_sort clonally dominant cardiomyocytes direct heart morphogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340018/
https://www.ncbi.nlm.nih.gov/pubmed/22538609
http://dx.doi.org/10.1038/nature11045
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