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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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.
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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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