Fate predetermination of cardiac myocytes during zebrafish heart regeneration

Adult zebrafish have the remarkable ability to regenerate their heart upon injury, a process that involves limited dedifferentiation and proliferation of spared cardiomyocytes (CMs), and migration of their progeny. During regeneration, proliferating CMs are detected throughout the myocardium, includ...

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Main Authors: Isil Tekeli, Anna Garcia-Puig, Mario Notari, Cristina García-Pastor, Isabelle Aujard, Ludovic Jullien, Angel Raya
Format: Article
Language:English
Published: The Royal Society 2017-01-01
Series:Open Biology
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.170116
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spelling doaj-6450bd0852a04144b99ca9cf3aed88bc2020-11-25T03:51:59ZengThe Royal SocietyOpen Biology2046-24412017-01-017610.1098/rsob.170116170116Fate predetermination of cardiac myocytes during zebrafish heart regenerationIsil TekeliAnna Garcia-PuigMario NotariCristina García-PastorIsabelle AujardLudovic JullienAngel RayaAdult zebrafish have the remarkable ability to regenerate their heart upon injury, a process that involves limited dedifferentiation and proliferation of spared cardiomyocytes (CMs), and migration of their progeny. During regeneration, proliferating CMs are detected throughout the myocardium, including areas distant to the injury site, but whether all of them are able to contribute to the regenerated tissue remains unknown. Here, we developed a CM-specific, photoinducible genetic labelling system, and show that CMs labelled in embryonic hearts survive and contribute to all three (primordial, trabecular and cortical) layers of the adult zebrafish heart. Next, using this system to investigate the fate of CMs from different parts of the myocardium during regeneration, we show that only CMs immediately adjacent to the injury site contributed to the regenerated tissue. Finally, our results show an extensive predetermination of CM fate during adult heart regeneration, with cells from each myocardial layer giving rise to cells that retain their layer identity in the regenerated myocardium. Overall, our results indicate that adult heart regeneration in the zebrafish is a rather static process governed by short-range signals, in contrast to the highly dynamic plasticity of CM fates that takes place during embryonic heart regeneration.https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.170116cardiomyocyteslineage-tracingcell migrationheart developmentcre/lox recombination
collection DOAJ
language English
format Article
sources DOAJ
author Isil Tekeli
Anna Garcia-Puig
Mario Notari
Cristina García-Pastor
Isabelle Aujard
Ludovic Jullien
Angel Raya
spellingShingle Isil Tekeli
Anna Garcia-Puig
Mario Notari
Cristina García-Pastor
Isabelle Aujard
Ludovic Jullien
Angel Raya
Fate predetermination of cardiac myocytes during zebrafish heart regeneration
Open Biology
cardiomyocytes
lineage-tracing
cell migration
heart development
cre/lox recombination
author_facet Isil Tekeli
Anna Garcia-Puig
Mario Notari
Cristina García-Pastor
Isabelle Aujard
Ludovic Jullien
Angel Raya
author_sort Isil Tekeli
title Fate predetermination of cardiac myocytes during zebrafish heart regeneration
title_short Fate predetermination of cardiac myocytes during zebrafish heart regeneration
title_full Fate predetermination of cardiac myocytes during zebrafish heart regeneration
title_fullStr Fate predetermination of cardiac myocytes during zebrafish heart regeneration
title_full_unstemmed Fate predetermination of cardiac myocytes during zebrafish heart regeneration
title_sort fate predetermination of cardiac myocytes during zebrafish heart regeneration
publisher The Royal Society
series Open Biology
issn 2046-2441
publishDate 2017-01-01
description Adult zebrafish have the remarkable ability to regenerate their heart upon injury, a process that involves limited dedifferentiation and proliferation of spared cardiomyocytes (CMs), and migration of their progeny. During regeneration, proliferating CMs are detected throughout the myocardium, including areas distant to the injury site, but whether all of them are able to contribute to the regenerated tissue remains unknown. Here, we developed a CM-specific, photoinducible genetic labelling system, and show that CMs labelled in embryonic hearts survive and contribute to all three (primordial, trabecular and cortical) layers of the adult zebrafish heart. Next, using this system to investigate the fate of CMs from different parts of the myocardium during regeneration, we show that only CMs immediately adjacent to the injury site contributed to the regenerated tissue. Finally, our results show an extensive predetermination of CM fate during adult heart regeneration, with cells from each myocardial layer giving rise to cells that retain their layer identity in the regenerated myocardium. Overall, our results indicate that adult heart regeneration in the zebrafish is a rather static process governed by short-range signals, in contrast to the highly dynamic plasticity of CM fates that takes place during embryonic heart regeneration.
topic cardiomyocytes
lineage-tracing
cell migration
heart development
cre/lox recombination
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.170116
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