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Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells

AIMS: There is strong evidence supporting the claim that endogenous cardiac progenitor cells (CPCs) are key players in cardiac regeneration, but the anatomic source and phenotype of the master cardiac progenitors remains uncertain. Our aim was to investigate the different cardiac stem cell populatio...

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Autores principales: Leinonen, Jussi V., Emanuelov, Avishag K., Platt, Yardanna, Helman, Yaron, Feinberg, Yael, Lotan, Chaim, Beeri, Ronen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595246/
https://www.ncbi.nlm.nih.gov/pubmed/23555001
http://dx.doi.org/10.1371/journal.pone.0059228
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author Leinonen, Jussi V.
Emanuelov, Avishag K.
Platt, Yardanna
Helman, Yaron
Feinberg, Yael
Lotan, Chaim
Beeri, Ronen
author_facet Leinonen, Jussi V.
Emanuelov, Avishag K.
Platt, Yardanna
Helman, Yaron
Feinberg, Yael
Lotan, Chaim
Beeri, Ronen
author_sort Leinonen, Jussi V.
collection PubMed
description AIMS: There is strong evidence supporting the claim that endogenous cardiac progenitor cells (CPCs) are key players in cardiac regeneration, but the anatomic source and phenotype of the master cardiac progenitors remains uncertain. Our aim was to investigate the different cardiac stem cell populations in the left atrial appendage (LAA) and their fates. METHODS AND RESULTS: We investigated the CPC content and profile of adult murine LAAs using immunohistochemistry and flow cytometry. We demonstrate that the LAA contains a large number of CPCs relative to other areas of the heart, representing over 20% of the total cell number. We grew two distinct CPC populations from the LAA by varying the degree of proteolysis. These differed by their histological location, surface marker profiles and growth dynamics. Specifically, CD45(pos) cells grew with milder proteolysis, while CD45(neg) cells grew mainly with more intense proteolysis. Both cell types could be induced to differentiate into cells with cardiomyocyte markers and organelles, albeit by different protocols. Many CD45(pos) cells expressed CD45 initially and rapidly lost its expression while differentiating. CONCLUSIONS: Our results demonstrate that the left atrial appendage plays a role as a reservoir of multiple types of progenitor cells in murine adult hearts. Two different types of CPCs were isolated, differing in their epicardial-myocardial localization. Considering studies demonstrating layer-specific origins of different cardiac progenitor cells, our findings may shed light on possible pathways to study and utilize the diversity of endogenous progenitor cells in the adult heart.
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spelling pubmed-35952462013-04-02 Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells Leinonen, Jussi V. Emanuelov, Avishag K. Platt, Yardanna Helman, Yaron Feinberg, Yael Lotan, Chaim Beeri, Ronen PLoS One Research Article AIMS: There is strong evidence supporting the claim that endogenous cardiac progenitor cells (CPCs) are key players in cardiac regeneration, but the anatomic source and phenotype of the master cardiac progenitors remains uncertain. Our aim was to investigate the different cardiac stem cell populations in the left atrial appendage (LAA) and their fates. METHODS AND RESULTS: We investigated the CPC content and profile of adult murine LAAs using immunohistochemistry and flow cytometry. We demonstrate that the LAA contains a large number of CPCs relative to other areas of the heart, representing over 20% of the total cell number. We grew two distinct CPC populations from the LAA by varying the degree of proteolysis. These differed by their histological location, surface marker profiles and growth dynamics. Specifically, CD45(pos) cells grew with milder proteolysis, while CD45(neg) cells grew mainly with more intense proteolysis. Both cell types could be induced to differentiate into cells with cardiomyocyte markers and organelles, albeit by different protocols. Many CD45(pos) cells expressed CD45 initially and rapidly lost its expression while differentiating. CONCLUSIONS: Our results demonstrate that the left atrial appendage plays a role as a reservoir of multiple types of progenitor cells in murine adult hearts. Two different types of CPCs were isolated, differing in their epicardial-myocardial localization. Considering studies demonstrating layer-specific origins of different cardiac progenitor cells, our findings may shed light on possible pathways to study and utilize the diversity of endogenous progenitor cells in the adult heart. Public Library of Science 2013-03-12 /pmc/articles/PMC3595246/ /pubmed/23555001 http://dx.doi.org/10.1371/journal.pone.0059228 Text en © 2013 Leinonen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Leinonen, Jussi V.
Emanuelov, Avishag K.
Platt, Yardanna
Helman, Yaron
Feinberg, Yael
Lotan, Chaim
Beeri, Ronen
Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells
title Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells
title_full Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells
title_fullStr Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells
title_full_unstemmed Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells
title_short Left Atrial Appendages from Adult Hearts Contain a Reservoir of Diverse Cardiac Progenitor Cells
title_sort left atrial appendages from adult hearts contain a reservoir of diverse cardiac progenitor cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595246/
https://www.ncbi.nlm.nih.gov/pubmed/23555001
http://dx.doi.org/10.1371/journal.pone.0059228
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