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Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids
Human amniotic fluid (hAF) cells share characteristics of both embryonic and adult stem cells. They proliferate rapidly and can differentiate into cells of all embryonic germ layers but do not form teratomas. Embryoid-bodies obtained from hAF have cardiac differentiation potential, but terminal diff...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089907/ https://www.ncbi.nlm.nih.gov/pubmed/30104705 http://dx.doi.org/10.1038/s41598-018-30537-z |
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author | Di Baldassarre, Angela D’Amico, Maria A Izzicupo, Pascal Gaggi, Giulia Guarnieri, Simone Mariggiò, Maria A Antonucci, Ivana Corneo, Barbara Sirabella, Dario Stuppia, Liborio Ghinassi, Barbara |
author_facet | Di Baldassarre, Angela D’Amico, Maria A Izzicupo, Pascal Gaggi, Giulia Guarnieri, Simone Mariggiò, Maria A Antonucci, Ivana Corneo, Barbara Sirabella, Dario Stuppia, Liborio Ghinassi, Barbara |
author_sort | Di Baldassarre, Angela |
collection | PubMed |
description | Human amniotic fluid (hAF) cells share characteristics of both embryonic and adult stem cells. They proliferate rapidly and can differentiate into cells of all embryonic germ layers but do not form teratomas. Embryoid-bodies obtained from hAF have cardiac differentiation potential, but terminal differentiation to cardiomyocytes (CMs) has not yet been described. Our purpose was to promote cardiac differentiation in hAFcells. Cells were exposed to inducing factors for up to 15 days. Only the subset of hAF cells expressing the multipotency markers SSEA4, OCT4 and CD90 ((Cardiopoietic)AF cells) responded to the differentiation process by increasing the expression of the cardiac transcription factors Nkx2.5 and GATA4, sarcomeric proteins (cTnT, α-MHC, α-SA), Connexin43 and atrial and ventricular markers. Furthermore, differentiated cells were positive for the calcium pumps CACNA1C and SERCA2a, with approximately 30% of (Cardiopoietic)AF-derived CM-like cells responding to caffeine or adrenergic stimulation. Some spontaneous rare beating foci were also observed. In conclusion, we demonstrated that (Cardiopoietic)AF cells might differentiate toward the cardiac lineage giving rise to CM-like cells characterized by several cardiac-specific molecular, structural, and functional properties. |
format | Online Article Text |
id | pubmed-6089907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60899072018-08-17 Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids Di Baldassarre, Angela D’Amico, Maria A Izzicupo, Pascal Gaggi, Giulia Guarnieri, Simone Mariggiò, Maria A Antonucci, Ivana Corneo, Barbara Sirabella, Dario Stuppia, Liborio Ghinassi, Barbara Sci Rep Article Human amniotic fluid (hAF) cells share characteristics of both embryonic and adult stem cells. They proliferate rapidly and can differentiate into cells of all embryonic germ layers but do not form teratomas. Embryoid-bodies obtained from hAF have cardiac differentiation potential, but terminal differentiation to cardiomyocytes (CMs) has not yet been described. Our purpose was to promote cardiac differentiation in hAFcells. Cells were exposed to inducing factors for up to 15 days. Only the subset of hAF cells expressing the multipotency markers SSEA4, OCT4 and CD90 ((Cardiopoietic)AF cells) responded to the differentiation process by increasing the expression of the cardiac transcription factors Nkx2.5 and GATA4, sarcomeric proteins (cTnT, α-MHC, α-SA), Connexin43 and atrial and ventricular markers. Furthermore, differentiated cells were positive for the calcium pumps CACNA1C and SERCA2a, with approximately 30% of (Cardiopoietic)AF-derived CM-like cells responding to caffeine or adrenergic stimulation. Some spontaneous rare beating foci were also observed. In conclusion, we demonstrated that (Cardiopoietic)AF cells might differentiate toward the cardiac lineage giving rise to CM-like cells characterized by several cardiac-specific molecular, structural, and functional properties. Nature Publishing Group UK 2018-08-13 /pmc/articles/PMC6089907/ /pubmed/30104705 http://dx.doi.org/10.1038/s41598-018-30537-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Di Baldassarre, Angela D’Amico, Maria A Izzicupo, Pascal Gaggi, Giulia Guarnieri, Simone Mariggiò, Maria A Antonucci, Ivana Corneo, Barbara Sirabella, Dario Stuppia, Liborio Ghinassi, Barbara Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids |
title | Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids |
title_full | Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids |
title_fullStr | Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids |
title_full_unstemmed | Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids |
title_short | Cardiomyocytes Derived from Human (Cardiopoietic)Amniotic Fluids |
title_sort | cardiomyocytes derived from human (cardiopoietic)amniotic fluids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089907/ https://www.ncbi.nlm.nih.gov/pubmed/30104705 http://dx.doi.org/10.1038/s41598-018-30537-z |
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