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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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 |
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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 |
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