Cargando…

APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells

Cardiomyocytes can be readily derived from human induced pluripotent stem cell (hiPSC) lines, yet its efficacy varies across different batches of the same and different hiPSC lines. To unravel the inconsistencies of in vitro cardiac differentiation, we utilized single cell transcriptomics on hiPSCs...

Descripción completa

Detalles Bibliográficos
Autores principales: Lam, Yin-Yu, Chan, Chun-Ho, Geng, Lin, Wong, Nicodemus, Keung, Wendy, Cheung, Yiu-Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395470/
https://www.ncbi.nlm.nih.gov/pubmed/37539315
http://dx.doi.org/10.1016/j.heliyon.2023.e18243
_version_ 1785083583823609856
author Lam, Yin-Yu
Chan, Chun-Ho
Geng, Lin
Wong, Nicodemus
Keung, Wendy
Cheung, Yiu-Fai
author_facet Lam, Yin-Yu
Chan, Chun-Ho
Geng, Lin
Wong, Nicodemus
Keung, Wendy
Cheung, Yiu-Fai
author_sort Lam, Yin-Yu
collection PubMed
description Cardiomyocytes can be readily derived from human induced pluripotent stem cell (hiPSC) lines, yet its efficacy varies across different batches of the same and different hiPSC lines. To unravel the inconsistencies of in vitro cardiac differentiation, we utilized single cell transcriptomics on hiPSCs undergoing cardiac differentiation and identified cardiac and extra-cardiac lineages throughout differentiation. We further identified APLNR as a surface marker for in vitro cardiac progenitors and immunomagnetically isolated them. Differentiation of isolated in vitro APLNR(+) cardiac progenitors derived from multiple hiPSC lines resulted in predominantly cardiomyocytes accompanied with cardiac mesenchyme. Transcriptomic analysis of differentiating in vitro APLNR(+) cardiac progenitors revealed transient expression of cardiac progenitor markers before further commitment into cardiomyocyte and cardiac mesenchyme. Analysis of in vivo human and mouse embryo single cell transcriptomic datasets have identified APLNR expression in early cardiac progenitors of multiple lineages. This platform enables generation of in vitro cardiac progenitors from multiple hiPSC lines without genetic manipulation, which has potential applications in studying cardiac development, disease modelling and cardiac regeneration.
format Online
Article
Text
id pubmed-10395470
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-103954702023-08-03 APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells Lam, Yin-Yu Chan, Chun-Ho Geng, Lin Wong, Nicodemus Keung, Wendy Cheung, Yiu-Fai Heliyon Research Article Cardiomyocytes can be readily derived from human induced pluripotent stem cell (hiPSC) lines, yet its efficacy varies across different batches of the same and different hiPSC lines. To unravel the inconsistencies of in vitro cardiac differentiation, we utilized single cell transcriptomics on hiPSCs undergoing cardiac differentiation and identified cardiac and extra-cardiac lineages throughout differentiation. We further identified APLNR as a surface marker for in vitro cardiac progenitors and immunomagnetically isolated them. Differentiation of isolated in vitro APLNR(+) cardiac progenitors derived from multiple hiPSC lines resulted in predominantly cardiomyocytes accompanied with cardiac mesenchyme. Transcriptomic analysis of differentiating in vitro APLNR(+) cardiac progenitors revealed transient expression of cardiac progenitor markers before further commitment into cardiomyocyte and cardiac mesenchyme. Analysis of in vivo human and mouse embryo single cell transcriptomic datasets have identified APLNR expression in early cardiac progenitors of multiple lineages. This platform enables generation of in vitro cardiac progenitors from multiple hiPSC lines without genetic manipulation, which has potential applications in studying cardiac development, disease modelling and cardiac regeneration. Elsevier 2023-07-13 /pmc/articles/PMC10395470/ /pubmed/37539315 http://dx.doi.org/10.1016/j.heliyon.2023.e18243 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Lam, Yin-Yu
Chan, Chun-Ho
Geng, Lin
Wong, Nicodemus
Keung, Wendy
Cheung, Yiu-Fai
APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
title APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
title_full APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
title_fullStr APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
title_full_unstemmed APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
title_short APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
title_sort aplnr marks a cardiac progenitor derived with human induced pluripotent stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395470/
https://www.ncbi.nlm.nih.gov/pubmed/37539315
http://dx.doi.org/10.1016/j.heliyon.2023.e18243
work_keys_str_mv AT lamyinyu aplnrmarksacardiacprogenitorderivedwithhumaninducedpluripotentstemcells
AT chanchunho aplnrmarksacardiacprogenitorderivedwithhumaninducedpluripotentstemcells
AT genglin aplnrmarksacardiacprogenitorderivedwithhumaninducedpluripotentstemcells
AT wongnicodemus aplnrmarksacardiacprogenitorderivedwithhumaninducedpluripotentstemcells
AT keungwendy aplnrmarksacardiacprogenitorderivedwithhumaninducedpluripotentstemcells
AT cheungyiufai aplnrmarksacardiacprogenitorderivedwithhumaninducedpluripotentstemcells