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Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo

Human dental pulp is a promising alternative source of stem cells for cell-based tissue engineering in regenerative medicine, for the easily recruitment with low invasivity for the patient and for the self-renewal and differentiation potential of cells. So far, in vitro culture of mesenchymal stem c...

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Autores principales: Pisciotta, Alessandra, Riccio, Massimo, Carnevale, Gianluca, Beretti, Francesca, Gibellini, Lara, Maraldi, Tullia, Cavallini, Gian Maria, Ferrari, Adriano, Bruzzesi, Giacomo, De Pol, Anto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510089/
https://www.ncbi.nlm.nih.gov/pubmed/23209773
http://dx.doi.org/10.1371/journal.pone.0050542
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author Pisciotta, Alessandra
Riccio, Massimo
Carnevale, Gianluca
Beretti, Francesca
Gibellini, Lara
Maraldi, Tullia
Cavallini, Gian Maria
Ferrari, Adriano
Bruzzesi, Giacomo
De Pol, Anto
author_facet Pisciotta, Alessandra
Riccio, Massimo
Carnevale, Gianluca
Beretti, Francesca
Gibellini, Lara
Maraldi, Tullia
Cavallini, Gian Maria
Ferrari, Adriano
Bruzzesi, Giacomo
De Pol, Anto
author_sort Pisciotta, Alessandra
collection PubMed
description Human dental pulp is a promising alternative source of stem cells for cell-based tissue engineering in regenerative medicine, for the easily recruitment with low invasivity for the patient and for the self-renewal and differentiation potential of cells. So far, in vitro culture of mesenchymal stem cells is usually based on supplementing culture and differentiation media with foetal calf serum (FCS). FCS is known to contain a great quantity of growth factors, and thus to promote cell attachment on plastic surface as well as expansion and differentiation. Nevertheless, FCS as an animal origin supplement may represent a potential means for disease transmission besides leading to a xenogenic immune response. Therefore, a significant interest is focused on investigating alternative supplements, in order to obtain a sufficient cell number for clinical application, avoiding the inconvenients of FCS use. In our study we have demonstrated that human serum (HS) is a suitable alternative to FCS, indeed its addition to culture medium induces a high hDPSCs proliferation rate and improves the in vitro osteogenic differentiation. Furthermore, hDPSCs-collagen constructs, pre-differentiated with HS-medium in vitro for 10 days, when implanted in immunocompromised rats, are able to restore critical size parietal bone defects. Therefore these data indicate that HS is a valid substitute for FCS to culture and differentiate in vitro hDPSCs in order to obtain a successful bone regeneration in vivo.
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spelling pubmed-35100892012-12-03 Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo Pisciotta, Alessandra Riccio, Massimo Carnevale, Gianluca Beretti, Francesca Gibellini, Lara Maraldi, Tullia Cavallini, Gian Maria Ferrari, Adriano Bruzzesi, Giacomo De Pol, Anto PLoS One Research Article Human dental pulp is a promising alternative source of stem cells for cell-based tissue engineering in regenerative medicine, for the easily recruitment with low invasivity for the patient and for the self-renewal and differentiation potential of cells. So far, in vitro culture of mesenchymal stem cells is usually based on supplementing culture and differentiation media with foetal calf serum (FCS). FCS is known to contain a great quantity of growth factors, and thus to promote cell attachment on plastic surface as well as expansion and differentiation. Nevertheless, FCS as an animal origin supplement may represent a potential means for disease transmission besides leading to a xenogenic immune response. Therefore, a significant interest is focused on investigating alternative supplements, in order to obtain a sufficient cell number for clinical application, avoiding the inconvenients of FCS use. In our study we have demonstrated that human serum (HS) is a suitable alternative to FCS, indeed its addition to culture medium induces a high hDPSCs proliferation rate and improves the in vitro osteogenic differentiation. Furthermore, hDPSCs-collagen constructs, pre-differentiated with HS-medium in vitro for 10 days, when implanted in immunocompromised rats, are able to restore critical size parietal bone defects. Therefore these data indicate that HS is a valid substitute for FCS to culture and differentiate in vitro hDPSCs in order to obtain a successful bone regeneration in vivo. Public Library of Science 2012-11-29 /pmc/articles/PMC3510089/ /pubmed/23209773 http://dx.doi.org/10.1371/journal.pone.0050542 Text en © 2012 Pisciotta et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pisciotta, Alessandra
Riccio, Massimo
Carnevale, Gianluca
Beretti, Francesca
Gibellini, Lara
Maraldi, Tullia
Cavallini, Gian Maria
Ferrari, Adriano
Bruzzesi, Giacomo
De Pol, Anto
Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo
title Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo
title_full Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo
title_fullStr Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo
title_full_unstemmed Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo
title_short Human Serum Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells In Vitro and In Vivo
title_sort human serum promotes osteogenic differentiation of human dental pulp stem cells in vitro and in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510089/
https://www.ncbi.nlm.nih.gov/pubmed/23209773
http://dx.doi.org/10.1371/journal.pone.0050542
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