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Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine

Recently, the development and the application of 3D scaffold able to promote stem cell differentiation represented an essential field of interest in regenerative medicine. In particular, functionalized scaffolds improve bone tissue formation and promote bone defects repair. This research aims to eva...

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Autores principales: Pizzicannella, Jacopo, Marconi, Guya D., Pierdomenico, Sante D., Cavalcanti, Marcos F.X.B., Diomede, Francesca, Trubiani, Oriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767323/
https://www.ncbi.nlm.nih.gov/pubmed/31696691
http://dx.doi.org/10.4081/ejh.2019.3064
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author Pizzicannella, Jacopo
Marconi, Guya D.
Pierdomenico, Sante D.
Cavalcanti, Marcos F.X.B.
Diomede, Francesca
Trubiani, Oriana
author_facet Pizzicannella, Jacopo
Marconi, Guya D.
Pierdomenico, Sante D.
Cavalcanti, Marcos F.X.B.
Diomede, Francesca
Trubiani, Oriana
author_sort Pizzicannella, Jacopo
collection PubMed
description Recently, the development and the application of 3D scaffold able to promote stem cell differentiation represented an essential field of interest in regenerative medicine. In particular, functionalized scaffolds improve bone tissue formation and promote bone defects repair. This research aims to evaluate the role of ascorbic acid (AS) supplementation in an in vitro model, in which a novel 3D-scaffold, bovine pericardium collagen membrane called BioRipar (BioR) was functionalized with human Gingival Mesenchymal Stem Cells (hGMSCs). As extensively reported in the literature, AS is an essential antioxidant molecule involved in the extracellular matrix secretion and in the osteogenic induction. Specifically, hGMSCs were seeded on BioR and treated with 60 and 90 μg/mL of AS in order to assess their growth behavior, the expression of bone specific markers involved in osteogenesis (runtrelated transcription factor 2, RUNX2; collagen1A1, COL1A1; osteopontin, OPN; bone morphogenetic protein2/4, BMP2/4), and de novo deposition of calcium. The expression of COL1A1, RUNX2, BMP2/4 and OPN was evaluated by RT-PCR, Western blotting and immunocytochemistry, and proved to be upregulated. Our results demonstrate that after three weeks of treatment AS at 60 and 90 μg/mL operates as an osteogenic inductor in hGMSCs. These data indicate that the AS supplementation produces an enhancement of osteogenic phenotype commitment in an in vitro environment. For this reason, AS could represent a valid support for basic and translational research in tissue engineering and regenerative medicine.
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spelling pubmed-67673232019-10-04 Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine Pizzicannella, Jacopo Marconi, Guya D. Pierdomenico, Sante D. Cavalcanti, Marcos F.X.B. Diomede, Francesca Trubiani, Oriana Eur J Histochem Original Paper Recently, the development and the application of 3D scaffold able to promote stem cell differentiation represented an essential field of interest in regenerative medicine. In particular, functionalized scaffolds improve bone tissue formation and promote bone defects repair. This research aims to evaluate the role of ascorbic acid (AS) supplementation in an in vitro model, in which a novel 3D-scaffold, bovine pericardium collagen membrane called BioRipar (BioR) was functionalized with human Gingival Mesenchymal Stem Cells (hGMSCs). As extensively reported in the literature, AS is an essential antioxidant molecule involved in the extracellular matrix secretion and in the osteogenic induction. Specifically, hGMSCs were seeded on BioR and treated with 60 and 90 μg/mL of AS in order to assess their growth behavior, the expression of bone specific markers involved in osteogenesis (runtrelated transcription factor 2, RUNX2; collagen1A1, COL1A1; osteopontin, OPN; bone morphogenetic protein2/4, BMP2/4), and de novo deposition of calcium. The expression of COL1A1, RUNX2, BMP2/4 and OPN was evaluated by RT-PCR, Western blotting and immunocytochemistry, and proved to be upregulated. Our results demonstrate that after three weeks of treatment AS at 60 and 90 μg/mL operates as an osteogenic inductor in hGMSCs. These data indicate that the AS supplementation produces an enhancement of osteogenic phenotype commitment in an in vitro environment. For this reason, AS could represent a valid support for basic and translational research in tissue engineering and regenerative medicine. PAGEPress Publications, Pavia, Italy 2019-09-25 /pmc/articles/PMC6767323/ /pubmed/31696691 http://dx.doi.org/10.4081/ejh.2019.3064 Text en ©Copyright: the Author(s), 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Pizzicannella, Jacopo
Marconi, Guya D.
Pierdomenico, Sante D.
Cavalcanti, Marcos F.X.B.
Diomede, Francesca
Trubiani, Oriana
Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine
title Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine
title_full Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine
title_fullStr Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine
title_full_unstemmed Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine
title_short Bovine pericardium membrane, gingival stem cells, and ascorbic acid: A novel team in regenerative medicine
title_sort bovine pericardium membrane, gingival stem cells, and ascorbic acid: a novel team in regenerative medicine
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767323/
https://www.ncbi.nlm.nih.gov/pubmed/31696691
http://dx.doi.org/10.4081/ejh.2019.3064
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