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Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells

The aim of this study was to evaluate the efficiency of ascorbic acid (AA) on cell viability, cytotoxicity and the effects on cardiomyogenic differentiation of the human amniotic fluid mesenchymal stem cells (hAF-MSCs). The results of methylthiazole tetrazolium (MTT) assay and cell apoptosis assay i...

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Autores principales: Markmee, Runchana, Aungsuchawan, Sirinda, Pothacharoen, Peraphan, Tancharoen, Waleephan, Narakornsak, Suteera, Laowanitwattana, Tanongsak, Bumroongkit, Kanokkan, Puaninta, Chaniporn, Pangjaidee, Nathaporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639694/
https://www.ncbi.nlm.nih.gov/pubmed/31360783
http://dx.doi.org/10.1016/j.heliyon.2019.e02018
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author Markmee, Runchana
Aungsuchawan, Sirinda
Pothacharoen, Peraphan
Tancharoen, Waleephan
Narakornsak, Suteera
Laowanitwattana, Tanongsak
Bumroongkit, Kanokkan
Puaninta, Chaniporn
Pangjaidee, Nathaporn
author_facet Markmee, Runchana
Aungsuchawan, Sirinda
Pothacharoen, Peraphan
Tancharoen, Waleephan
Narakornsak, Suteera
Laowanitwattana, Tanongsak
Bumroongkit, Kanokkan
Puaninta, Chaniporn
Pangjaidee, Nathaporn
author_sort Markmee, Runchana
collection PubMed
description The aim of this study was to evaluate the efficiency of ascorbic acid (AA) on cell viability, cytotoxicity and the effects on cardiomyogenic differentiation of the human amniotic fluid mesenchymal stem cells (hAF-MSCs). The results of methylthiazole tetrazolium (MTT) assay and cell apoptosis assay indicated that after 24, 48 and 72 h of treatment, AA had no effect on cells viability and cytotoxicity. After treating the hAF-MSCs with 5-azacytidine (5-aza) and a combination of AA and 5-aza, the alamar blue cells proliferation assay showed the normal growth characteristic similar to control group. Especially, the morphological changes were observed between day 0 and day 21, and it was revealed that the hAF-MSCs exhibited myotube-like morphology after 7 days of cell culturing. Moreover, the treatment with a combination of AA and 5-aza was able to up-regulate the cardiomyogenic specific gene levels, which are known to play an important role in cardiomyogenesis. This was specifically notable with the results of immunofluorescence and immunoenzymatic staining in the AA combined with 5-aza treatment group, the highest expression of cardiomyogenic specific proteins was revealed including for GATA4, cTnT, Cx43 and Nkx2.5. It could be concluded that AA may be a good alternative cardiomyogenic inducing factor for hAF-MSCs and may open new insights into future biomedical applications for a clinically treatment.
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spelling pubmed-66396942019-07-29 Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells Markmee, Runchana Aungsuchawan, Sirinda Pothacharoen, Peraphan Tancharoen, Waleephan Narakornsak, Suteera Laowanitwattana, Tanongsak Bumroongkit, Kanokkan Puaninta, Chaniporn Pangjaidee, Nathaporn Heliyon Article The aim of this study was to evaluate the efficiency of ascorbic acid (AA) on cell viability, cytotoxicity and the effects on cardiomyogenic differentiation of the human amniotic fluid mesenchymal stem cells (hAF-MSCs). The results of methylthiazole tetrazolium (MTT) assay and cell apoptosis assay indicated that after 24, 48 and 72 h of treatment, AA had no effect on cells viability and cytotoxicity. After treating the hAF-MSCs with 5-azacytidine (5-aza) and a combination of AA and 5-aza, the alamar blue cells proliferation assay showed the normal growth characteristic similar to control group. Especially, the morphological changes were observed between day 0 and day 21, and it was revealed that the hAF-MSCs exhibited myotube-like morphology after 7 days of cell culturing. Moreover, the treatment with a combination of AA and 5-aza was able to up-regulate the cardiomyogenic specific gene levels, which are known to play an important role in cardiomyogenesis. This was specifically notable with the results of immunofluorescence and immunoenzymatic staining in the AA combined with 5-aza treatment group, the highest expression of cardiomyogenic specific proteins was revealed including for GATA4, cTnT, Cx43 and Nkx2.5. It could be concluded that AA may be a good alternative cardiomyogenic inducing factor for hAF-MSCs and may open new insights into future biomedical applications for a clinically treatment. Elsevier 2019-07-17 /pmc/articles/PMC6639694/ /pubmed/31360783 http://dx.doi.org/10.1016/j.heliyon.2019.e02018 Text en © 2019 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
Markmee, Runchana
Aungsuchawan, Sirinda
Pothacharoen, Peraphan
Tancharoen, Waleephan
Narakornsak, Suteera
Laowanitwattana, Tanongsak
Bumroongkit, Kanokkan
Puaninta, Chaniporn
Pangjaidee, Nathaporn
Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
title Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
title_full Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
title_fullStr Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
title_full_unstemmed Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
title_short Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
title_sort effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639694/
https://www.ncbi.nlm.nih.gov/pubmed/31360783
http://dx.doi.org/10.1016/j.heliyon.2019.e02018
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