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Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are a powerful platform for biomedical research. However, they are immature, which is a barrier to modeling adult-onset cardiovascular disease. Here, we sought to develop a simple method that could drive cultured hiPSC-CMs toward...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940251/ https://www.ncbi.nlm.nih.gov/pubmed/33636116 http://dx.doi.org/10.1016/j.stemcr.2021.01.018 |
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author | Knight, Walter E. Cao, Yingqiong Lin, Ying-Hsi Chi, Congwu Bai, Betty Sparagna, Genevieve C. Zhao, Yuanbiao Du, Yanmei Londono, Pilar Reisz, Julie A. Brown, Benjamin C. Taylor, Matthew R.G. Ambardekar, Amrut V. Cleveland, Joseph C. McKinsey, Timothy A. Jeong, Mark Y. Walker, Lori A. Woulfe, Kathleen C. D'Alessandro, Angelo Chatfield, Kathryn C. Xu, Hongyan Bristow, Michael R. Buttrick, Peter M. Song, Kunhua |
author_facet | Knight, Walter E. Cao, Yingqiong Lin, Ying-Hsi Chi, Congwu Bai, Betty Sparagna, Genevieve C. Zhao, Yuanbiao Du, Yanmei Londono, Pilar Reisz, Julie A. Brown, Benjamin C. Taylor, Matthew R.G. Ambardekar, Amrut V. Cleveland, Joseph C. McKinsey, Timothy A. Jeong, Mark Y. Walker, Lori A. Woulfe, Kathleen C. D'Alessandro, Angelo Chatfield, Kathryn C. Xu, Hongyan Bristow, Michael R. Buttrick, Peter M. Song, Kunhua |
author_sort | Knight, Walter E. |
collection | PubMed |
description | Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are a powerful platform for biomedical research. However, they are immature, which is a barrier to modeling adult-onset cardiovascular disease. Here, we sought to develop a simple method that could drive cultured hiPSC-CMs toward maturity across a number of phenotypes, with the aim of utilizing mature hiPSC-CMs to model human cardiovascular disease. hiPSC-CMs were cultured in fatty acid-based medium and plated on micropatterned surfaces. These cells display many characteristics of adult human cardiomyocytes, including elongated cell morphology, sarcomeric maturity, and increased myofibril contractile force. In addition, mature hiPSC-CMs develop pathological hypertrophy, with associated myofibril relaxation defects, in response to either a pro-hypertrophic agent or genetic mutations. The more mature hiPSC-CMs produced by these methods could serve as a useful in vitro platform for characterizing cardiovascular disease. |
format | Online Article Text |
id | pubmed-7940251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79402512021-03-16 Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy Knight, Walter E. Cao, Yingqiong Lin, Ying-Hsi Chi, Congwu Bai, Betty Sparagna, Genevieve C. Zhao, Yuanbiao Du, Yanmei Londono, Pilar Reisz, Julie A. Brown, Benjamin C. Taylor, Matthew R.G. Ambardekar, Amrut V. Cleveland, Joseph C. McKinsey, Timothy A. Jeong, Mark Y. Walker, Lori A. Woulfe, Kathleen C. D'Alessandro, Angelo Chatfield, Kathryn C. Xu, Hongyan Bristow, Michael R. Buttrick, Peter M. Song, Kunhua Stem Cell Reports Article Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are a powerful platform for biomedical research. However, they are immature, which is a barrier to modeling adult-onset cardiovascular disease. Here, we sought to develop a simple method that could drive cultured hiPSC-CMs toward maturity across a number of phenotypes, with the aim of utilizing mature hiPSC-CMs to model human cardiovascular disease. hiPSC-CMs were cultured in fatty acid-based medium and plated on micropatterned surfaces. These cells display many characteristics of adult human cardiomyocytes, including elongated cell morphology, sarcomeric maturity, and increased myofibril contractile force. In addition, mature hiPSC-CMs develop pathological hypertrophy, with associated myofibril relaxation defects, in response to either a pro-hypertrophic agent or genetic mutations. The more mature hiPSC-CMs produced by these methods could serve as a useful in vitro platform for characterizing cardiovascular disease. Elsevier 2021-02-25 /pmc/articles/PMC7940251/ /pubmed/33636116 http://dx.doi.org/10.1016/j.stemcr.2021.01.018 Text en © 2021 The Authors http://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 | Article Knight, Walter E. Cao, Yingqiong Lin, Ying-Hsi Chi, Congwu Bai, Betty Sparagna, Genevieve C. Zhao, Yuanbiao Du, Yanmei Londono, Pilar Reisz, Julie A. Brown, Benjamin C. Taylor, Matthew R.G. Ambardekar, Amrut V. Cleveland, Joseph C. McKinsey, Timothy A. Jeong, Mark Y. Walker, Lori A. Woulfe, Kathleen C. D'Alessandro, Angelo Chatfield, Kathryn C. Xu, Hongyan Bristow, Michael R. Buttrick, Peter M. Song, Kunhua Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy |
title | Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy |
title_full | Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy |
title_fullStr | Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy |
title_full_unstemmed | Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy |
title_short | Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy |
title_sort | maturation of pluripotent stem cell-derived cardiomyocytes enables modeling of human hypertrophic cardiomyopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940251/ https://www.ncbi.nlm.nih.gov/pubmed/33636116 http://dx.doi.org/10.1016/j.stemcr.2021.01.018 |
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