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Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells

Background. Human induced pluripotent stem cells (iPSCs) are an attractive source of cardiomyocytes for cardiac repair and regeneration. In this study, we aim to determine whether acute electrical stimulation of human iPSCs can promote their differentiation to cardiomyocytes. Methods. Human iPSCs we...

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Autores principales: Hernández, Damián, Millard, Rodney, Sivakumaran, Priyadharshini, Wong, Raymond C. B., Crombie, Duncan E., Hewitt, Alex W., Liang, Helena, Hung, Sandy S. C., Pébay, Alice, Shepherd, Robert K., Dusting, Gregory J., Lim, Shiang Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691644/
https://www.ncbi.nlm.nih.gov/pubmed/26788064
http://dx.doi.org/10.1155/2016/1718041
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author Hernández, Damián
Millard, Rodney
Sivakumaran, Priyadharshini
Wong, Raymond C. B.
Crombie, Duncan E.
Hewitt, Alex W.
Liang, Helena
Hung, Sandy S. C.
Pébay, Alice
Shepherd, Robert K.
Dusting, Gregory J.
Lim, Shiang Y.
author_facet Hernández, Damián
Millard, Rodney
Sivakumaran, Priyadharshini
Wong, Raymond C. B.
Crombie, Duncan E.
Hewitt, Alex W.
Liang, Helena
Hung, Sandy S. C.
Pébay, Alice
Shepherd, Robert K.
Dusting, Gregory J.
Lim, Shiang Y.
author_sort Hernández, Damián
collection PubMed
description Background. Human induced pluripotent stem cells (iPSCs) are an attractive source of cardiomyocytes for cardiac repair and regeneration. In this study, we aim to determine whether acute electrical stimulation of human iPSCs can promote their differentiation to cardiomyocytes. Methods. Human iPSCs were differentiated to cardiac cells by forming embryoid bodies (EBs) for 5 days. EBs were then subjected to brief electrical stimulation and plated down for 14 days. Results. In iPS(Foreskin)-2 cell line, brief electrical stimulation at 65 mV/mm or 200 mV/mm for 5 min significantly increased the percentage of beating EBs present by day 14 after plating. Acute electrical stimulation also significantly increased the cardiac gene expression of ACTC1, TNNT2, MYH7, and MYL7. However, the cardiogenic effect of electrical stimulation was not reproducible in another iPS cell line, CERA007c6. Beating EBs from control and electrically stimulated groups expressed various cardiac-specific transcription factors and contractile muscle markers. Beating EBs were also shown to cycle calcium and were responsive to the chronotropic agents, isoproterenol and carbamylcholine, in a concentration-dependent manner. Conclusions. Our results demonstrate that brief electrical stimulation can promote cardiac differentiation of human iPS cells. The cardiogenic effect of brief electrical stimulation is dependent on the cell line used.
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spelling pubmed-46916442016-01-19 Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells Hernández, Damián Millard, Rodney Sivakumaran, Priyadharshini Wong, Raymond C. B. Crombie, Duncan E. Hewitt, Alex W. Liang, Helena Hung, Sandy S. C. Pébay, Alice Shepherd, Robert K. Dusting, Gregory J. Lim, Shiang Y. Stem Cells Int Research Article Background. Human induced pluripotent stem cells (iPSCs) are an attractive source of cardiomyocytes for cardiac repair and regeneration. In this study, we aim to determine whether acute electrical stimulation of human iPSCs can promote their differentiation to cardiomyocytes. Methods. Human iPSCs were differentiated to cardiac cells by forming embryoid bodies (EBs) for 5 days. EBs were then subjected to brief electrical stimulation and plated down for 14 days. Results. In iPS(Foreskin)-2 cell line, brief electrical stimulation at 65 mV/mm or 200 mV/mm for 5 min significantly increased the percentage of beating EBs present by day 14 after plating. Acute electrical stimulation also significantly increased the cardiac gene expression of ACTC1, TNNT2, MYH7, and MYL7. However, the cardiogenic effect of electrical stimulation was not reproducible in another iPS cell line, CERA007c6. Beating EBs from control and electrically stimulated groups expressed various cardiac-specific transcription factors and contractile muscle markers. Beating EBs were also shown to cycle calcium and were responsive to the chronotropic agents, isoproterenol and carbamylcholine, in a concentration-dependent manner. Conclusions. Our results demonstrate that brief electrical stimulation can promote cardiac differentiation of human iPS cells. The cardiogenic effect of brief electrical stimulation is dependent on the cell line used. Hindawi Publishing Corporation 2016 2015-12-14 /pmc/articles/PMC4691644/ /pubmed/26788064 http://dx.doi.org/10.1155/2016/1718041 Text en Copyright © 2016 Damián Hernández et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hernández, Damián
Millard, Rodney
Sivakumaran, Priyadharshini
Wong, Raymond C. B.
Crombie, Duncan E.
Hewitt, Alex W.
Liang, Helena
Hung, Sandy S. C.
Pébay, Alice
Shepherd, Robert K.
Dusting, Gregory J.
Lim, Shiang Y.
Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells
title Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells
title_full Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells
title_fullStr Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells
title_full_unstemmed Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells
title_short Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells
title_sort electrical stimulation promotes cardiac differentiation of human induced pluripotent stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691644/
https://www.ncbi.nlm.nih.gov/pubmed/26788064
http://dx.doi.org/10.1155/2016/1718041
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