Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.

The use of human stem cell-derived cardiomyocytes to study atrial biology and disease has been restricted by the lack of a reliable method for stem cell-derived atrial cell labeling and purification. The goal of this study was to generate an atrial-specific reporter construct to identify and purify...

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Main Authors: Rebecca Josowitz, Jia Lu, Christine Falce, Sunita L D'Souza, Meng Wu, Ninette Cohen, Nicole C Dubois, Yong Zhao, Eric A Sobie, Glenn I Fishman, Bruce D Gelb
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4092021?pdf=render
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spelling doaj-5826540853ae47d1bb19e0620eb13a832020-11-24T22:06:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0197e10131610.1371/journal.pone.0101316Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.Rebecca JosowitzJia LuChristine FalceSunita L D'SouzaMeng WuNinette CohenNicole C DuboisYong ZhaoEric A SobieGlenn I FishmanBruce D GelbThe use of human stem cell-derived cardiomyocytes to study atrial biology and disease has been restricted by the lack of a reliable method for stem cell-derived atrial cell labeling and purification. The goal of this study was to generate an atrial-specific reporter construct to identify and purify human stem cell-derived atrial-like cardiomyocytes. We have created a bacterial artificial chromosome (BAC) reporter construct in which fluorescence is driven by expression of the atrial-specific gene sarcolipin (SLN). When purified using flow cytometry, cells with high fluorescence specifically express atrial genes and display functional calcium handling and electrophysiological properties consistent with atrial cardiomyocytes. Our data indicate that SLN can be used as a marker to successfully monitor and isolate hiPSC-derived atrial-like cardiomyocytes. These purified cells may find many applications, including in the study of atrial-specific pathologies and chamber-specific lineage development.http://europepmc.org/articles/PMC4092021?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rebecca Josowitz
Jia Lu
Christine Falce
Sunita L D'Souza
Meng Wu
Ninette Cohen
Nicole C Dubois
Yong Zhao
Eric A Sobie
Glenn I Fishman
Bruce D Gelb
spellingShingle Rebecca Josowitz
Jia Lu
Christine Falce
Sunita L D'Souza
Meng Wu
Ninette Cohen
Nicole C Dubois
Yong Zhao
Eric A Sobie
Glenn I Fishman
Bruce D Gelb
Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
PLoS ONE
author_facet Rebecca Josowitz
Jia Lu
Christine Falce
Sunita L D'Souza
Meng Wu
Ninette Cohen
Nicole C Dubois
Yong Zhao
Eric A Sobie
Glenn I Fishman
Bruce D Gelb
author_sort Rebecca Josowitz
title Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
title_short Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
title_full Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
title_fullStr Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
title_full_unstemmed Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
title_sort identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description The use of human stem cell-derived cardiomyocytes to study atrial biology and disease has been restricted by the lack of a reliable method for stem cell-derived atrial cell labeling and purification. The goal of this study was to generate an atrial-specific reporter construct to identify and purify human stem cell-derived atrial-like cardiomyocytes. We have created a bacterial artificial chromosome (BAC) reporter construct in which fluorescence is driven by expression of the atrial-specific gene sarcolipin (SLN). When purified using flow cytometry, cells with high fluorescence specifically express atrial genes and display functional calcium handling and electrophysiological properties consistent with atrial cardiomyocytes. Our data indicate that SLN can be used as a marker to successfully monitor and isolate hiPSC-derived atrial-like cardiomyocytes. These purified cells may find many applications, including in the study of atrial-specific pathologies and chamber-specific lineage development.
url http://europepmc.org/articles/PMC4092021?pdf=render
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