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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6639694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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