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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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