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The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells

Amniotic fluid represents a new and promising source of engraftable stem cells. The purpose of this study was to investigate the in vitro effects of platelet-rich plasma (PRP) on amniotic-fluid-derived stem cells (AFSCs) on chondrogenic or osteogenic differentiation potential. Amniotic fluid samples...

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Autores principales: Giannetti, Alessio, Pantalone, Andrea, Antonucci, Ivana, Verna, Sandra, Di Gregorio, Patrizia, Stuppia, Liborio, Calvisi, Vittorio, Buda, Roberto, Salini, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738099/
https://www.ncbi.nlm.nih.gov/pubmed/36497861
http://dx.doi.org/10.3390/ijerph192315786
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author Giannetti, Alessio
Pantalone, Andrea
Antonucci, Ivana
Verna, Sandra
Di Gregorio, Patrizia
Stuppia, Liborio
Calvisi, Vittorio
Buda, Roberto
Salini, Vincenzo
author_facet Giannetti, Alessio
Pantalone, Andrea
Antonucci, Ivana
Verna, Sandra
Di Gregorio, Patrizia
Stuppia, Liborio
Calvisi, Vittorio
Buda, Roberto
Salini, Vincenzo
author_sort Giannetti, Alessio
collection PubMed
description Amniotic fluid represents a new and promising source of engraftable stem cells. The purpose of this study was to investigate the in vitro effects of platelet-rich plasma (PRP) on amniotic-fluid-derived stem cells (AFSCs) on chondrogenic or osteogenic differentiation potential. Amniotic fluid samples were obtained from women undergoing amniocentesis for prenatal diagnosis at 16–18 weeks of pregnancy. Undifferentiated human AFSCs were cocultured with PRP for 14 days. The study includes two protocols investigating the effects of activated PRP using two different methods: via freeze–thaw cycles and via the addition of calcium gluconate. On the 14th day of culturing, the differentiation potential of the cocultured AFSCs was then compared with undifferentiated AFSCs. Staining with alcian blue solution (ABS) and alizarine red solution (ARS) was performed, and chondrogenic- and osteogenic-associated genes markers were investigated. ABS demonstrated enhanced glycosaminoglycan expression. Cocultured cells expressed chondrocyte-associated genes, determined by real-time polymerase chain reaction (RT-PCR), including type I collagen, type II collagen, COMP, and aggrecan. In regard to the osteogenic markers, osteopontin and bone sialoprotein, there were no changes. In particular, the activation of PRP using the freeze–thaw cycle protocol showed a higher expression of the chondrogenic markers. Our preliminary in vitro results showed that PRP has good potential in the chondrogenic differentiation of AFSCs.
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spelling pubmed-97380992022-12-11 The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells Giannetti, Alessio Pantalone, Andrea Antonucci, Ivana Verna, Sandra Di Gregorio, Patrizia Stuppia, Liborio Calvisi, Vittorio Buda, Roberto Salini, Vincenzo Int J Environ Res Public Health Article Amniotic fluid represents a new and promising source of engraftable stem cells. The purpose of this study was to investigate the in vitro effects of platelet-rich plasma (PRP) on amniotic-fluid-derived stem cells (AFSCs) on chondrogenic or osteogenic differentiation potential. Amniotic fluid samples were obtained from women undergoing amniocentesis for prenatal diagnosis at 16–18 weeks of pregnancy. Undifferentiated human AFSCs were cocultured with PRP for 14 days. The study includes two protocols investigating the effects of activated PRP using two different methods: via freeze–thaw cycles and via the addition of calcium gluconate. On the 14th day of culturing, the differentiation potential of the cocultured AFSCs was then compared with undifferentiated AFSCs. Staining with alcian blue solution (ABS) and alizarine red solution (ARS) was performed, and chondrogenic- and osteogenic-associated genes markers were investigated. ABS demonstrated enhanced glycosaminoglycan expression. Cocultured cells expressed chondrocyte-associated genes, determined by real-time polymerase chain reaction (RT-PCR), including type I collagen, type II collagen, COMP, and aggrecan. In regard to the osteogenic markers, osteopontin and bone sialoprotein, there were no changes. In particular, the activation of PRP using the freeze–thaw cycle protocol showed a higher expression of the chondrogenic markers. Our preliminary in vitro results showed that PRP has good potential in the chondrogenic differentiation of AFSCs. MDPI 2022-11-27 /pmc/articles/PMC9738099/ /pubmed/36497861 http://dx.doi.org/10.3390/ijerph192315786 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giannetti, Alessio
Pantalone, Andrea
Antonucci, Ivana
Verna, Sandra
Di Gregorio, Patrizia
Stuppia, Liborio
Calvisi, Vittorio
Buda, Roberto
Salini, Vincenzo
The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells
title The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells
title_full The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells
title_fullStr The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells
title_full_unstemmed The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells
title_short The Role of Platelet-Rich Plasma on the Chondrogenic and Osteogenic Differentiation of Human Amniotic-Fluid-Derived Stem Cells
title_sort role of platelet-rich plasma on the chondrogenic and osteogenic differentiation of human amniotic-fluid-derived stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738099/
https://www.ncbi.nlm.nih.gov/pubmed/36497861
http://dx.doi.org/10.3390/ijerph192315786
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