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Differentiation of human adipose-derived stem cells into beating cardiomyocytes
Human adipose-derived stem cells (ASCs) may differentiate into cardiomyocytes and this provides a source of donor cells for tissue engineering. In this study, we evaluated cardiomyogenic differentiation protocols using a DNA demethylating agent 5-azacytidine (5-aza), a modified cardiomyogenic medium...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823119/ https://www.ncbi.nlm.nih.gov/pubmed/20070436 http://dx.doi.org/10.1111/j.1582-4934.2010.01009.x |
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author | Choi, Yu Suk Dusting, Gregory J Stubbs, Samantha Arunothayaraj, Sandeep Han, Xiao Lian Collas, Philippe Morrison, Wayne A Dilley, Rodney J |
author_facet | Choi, Yu Suk Dusting, Gregory J Stubbs, Samantha Arunothayaraj, Sandeep Han, Xiao Lian Collas, Philippe Morrison, Wayne A Dilley, Rodney J |
author_sort | Choi, Yu Suk |
collection | PubMed |
description | Human adipose-derived stem cells (ASCs) may differentiate into cardiomyocytes and this provides a source of donor cells for tissue engineering. In this study, we evaluated cardiomyogenic differentiation protocols using a DNA demethylating agent 5-azacytidine (5-aza), a modified cardiomyogenic medium (MCM), a histone deacetylase inhibitor trichostatin A (TSA) and co-culture with neonatal rat cardiomyocytes. 5-aza treatment reduced both cardiac actin and TropT mRNA expression. Incubation in MCM only slightly increased gene expression (1.5- to 1.9-fold) and the number of cells co-expressing nkx2.5/sarcomeric α-actin (27.2%versus 0.2% in control). TSA treatment increased cardiac actin mRNA expression 11-fold after 1 week, which could be sustained for 2 weeks by culturing cells in cardiomyocyte culture medium. TSA-treated cells also stained positively for cardiac myosin heavy chain, α-actin, TropI and connexin43; however, none of these treatments produced beating cells. ASCs in non-contact co-culture showed no cardiac differentiation; however, ASCs co-cultured in direct contact co-culture exhibited a time-dependent increase in cardiac actin mRNA expression (up to 33-fold) between days 3 and 14. Immunocytochemistry revealed co-expression of GATA4 and Nkx2.5, α-actin, TropI and cardiac myosin heavy chain in CM-DiI labelled ASCs. Most importantly, many of these cells showed spontaneous contractions accompanied by calcium transients in culture. Human ASC (hASC) showed synchronous Ca(2+) transient and contraction synchronous with surrounding rat cardiomyocytes (106 beats/min.). Gap junctions also formed between them as observed by dye transfer. In conclusion, cell-to-cell interaction was identified as a key inducer for cardiomyogenic differentiation of hASCs. This method was optimized by co-culture with contracting cardiomyocytes and provides a potential cardiac differentiation system to progress applications for cardiac cell therapy or tissue engineering. |
format | Online Article Text |
id | pubmed-3823119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38231192015-04-20 Differentiation of human adipose-derived stem cells into beating cardiomyocytes Choi, Yu Suk Dusting, Gregory J Stubbs, Samantha Arunothayaraj, Sandeep Han, Xiao Lian Collas, Philippe Morrison, Wayne A Dilley, Rodney J J Cell Mol Med Jcmm Express Human adipose-derived stem cells (ASCs) may differentiate into cardiomyocytes and this provides a source of donor cells for tissue engineering. In this study, we evaluated cardiomyogenic differentiation protocols using a DNA demethylating agent 5-azacytidine (5-aza), a modified cardiomyogenic medium (MCM), a histone deacetylase inhibitor trichostatin A (TSA) and co-culture with neonatal rat cardiomyocytes. 5-aza treatment reduced both cardiac actin and TropT mRNA expression. Incubation in MCM only slightly increased gene expression (1.5- to 1.9-fold) and the number of cells co-expressing nkx2.5/sarcomeric α-actin (27.2%versus 0.2% in control). TSA treatment increased cardiac actin mRNA expression 11-fold after 1 week, which could be sustained for 2 weeks by culturing cells in cardiomyocyte culture medium. TSA-treated cells also stained positively for cardiac myosin heavy chain, α-actin, TropI and connexin43; however, none of these treatments produced beating cells. ASCs in non-contact co-culture showed no cardiac differentiation; however, ASCs co-cultured in direct contact co-culture exhibited a time-dependent increase in cardiac actin mRNA expression (up to 33-fold) between days 3 and 14. Immunocytochemistry revealed co-expression of GATA4 and Nkx2.5, α-actin, TropI and cardiac myosin heavy chain in CM-DiI labelled ASCs. Most importantly, many of these cells showed spontaneous contractions accompanied by calcium transients in culture. Human ASC (hASC) showed synchronous Ca(2+) transient and contraction synchronous with surrounding rat cardiomyocytes (106 beats/min.). Gap junctions also formed between them as observed by dye transfer. In conclusion, cell-to-cell interaction was identified as a key inducer for cardiomyogenic differentiation of hASCs. This method was optimized by co-culture with contracting cardiomyocytes and provides a potential cardiac differentiation system to progress applications for cardiac cell therapy or tissue engineering. Blackwell Publishing Ltd 2010-04 2010-01-11 /pmc/articles/PMC3823119/ /pubmed/20070436 http://dx.doi.org/10.1111/j.1582-4934.2010.01009.x Text en © 2010 The Authors Journal compilation © 2010 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd |
spellingShingle | Jcmm Express Choi, Yu Suk Dusting, Gregory J Stubbs, Samantha Arunothayaraj, Sandeep Han, Xiao Lian Collas, Philippe Morrison, Wayne A Dilley, Rodney J Differentiation of human adipose-derived stem cells into beating cardiomyocytes |
title | Differentiation of human adipose-derived stem cells into beating cardiomyocytes |
title_full | Differentiation of human adipose-derived stem cells into beating cardiomyocytes |
title_fullStr | Differentiation of human adipose-derived stem cells into beating cardiomyocytes |
title_full_unstemmed | Differentiation of human adipose-derived stem cells into beating cardiomyocytes |
title_short | Differentiation of human adipose-derived stem cells into beating cardiomyocytes |
title_sort | differentiation of human adipose-derived stem cells into beating cardiomyocytes |
topic | Jcmm Express |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823119/ https://www.ncbi.nlm.nih.gov/pubmed/20070436 http://dx.doi.org/10.1111/j.1582-4934.2010.01009.x |
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