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Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies

Regenerative strategies for human articular cartilage are still challenging despite the presence of resident progenitor cell population. Today, many efforts in the field of regenerative medicine focus on the use of platelet derivatives due to their ability to reactivate endogenous mechanisms support...

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Autores principales: Carluccio, Simonetta, Martinelli, Daniela, Palamà, Maria Elisabetta Federica, Pereira, Rui Cruz, Benelli, Roberto, Guijarro, Ana, Cancedda, Ranieri, Gentili, Chiara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226425/
https://www.ncbi.nlm.nih.gov/pubmed/32340136
http://dx.doi.org/10.3390/cells9041052
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author Carluccio, Simonetta
Martinelli, Daniela
Palamà, Maria Elisabetta Federica
Pereira, Rui Cruz
Benelli, Roberto
Guijarro, Ana
Cancedda, Ranieri
Gentili, Chiara
author_facet Carluccio, Simonetta
Martinelli, Daniela
Palamà, Maria Elisabetta Federica
Pereira, Rui Cruz
Benelli, Roberto
Guijarro, Ana
Cancedda, Ranieri
Gentili, Chiara
author_sort Carluccio, Simonetta
collection PubMed
description Regenerative strategies for human articular cartilage are still challenging despite the presence of resident progenitor cell population. Today, many efforts in the field of regenerative medicine focus on the use of platelet derivatives due to their ability to reactivate endogenous mechanisms supporting tissue repair. While their use in orthopedics continues, mechanisms of action and efficacy need further characterization. We describe that the platelet lysate (PL) is able to activate chondro-progenitor cells in a terminally differentiated cartilage tissue. Primary cultures of human articular chondrocytes (ACs) and cartilage explants were set up from donor hip joint biopsies and were treated in vitro with PL. PL recruited a chondro-progenitors (CPCs)-enriched population from ex vivo cartilage culture, that showed high proliferation rate, clonogenicity and nestin expression. CPCs were positive for in vitro tri-lineage differentiation and formed hyaline cartilage-like tissue in vivo without hypertrophic fate. Moreover, the secretory profile of CPCs was analyzed, together with their migratory capabilities. Some CPC-features were also induced in PL-treated ACs compared to fetal bovine serum (FBS)-control ACs. PL treatment of human articular cartilage activates a stem cell niche responsive to injury. These facts can improve the PL therapeutic efficacy in cartilage applications.
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spelling pubmed-72264252020-05-18 Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies Carluccio, Simonetta Martinelli, Daniela Palamà, Maria Elisabetta Federica Pereira, Rui Cruz Benelli, Roberto Guijarro, Ana Cancedda, Ranieri Gentili, Chiara Cells Article Regenerative strategies for human articular cartilage are still challenging despite the presence of resident progenitor cell population. Today, many efforts in the field of regenerative medicine focus on the use of platelet derivatives due to their ability to reactivate endogenous mechanisms supporting tissue repair. While their use in orthopedics continues, mechanisms of action and efficacy need further characterization. We describe that the platelet lysate (PL) is able to activate chondro-progenitor cells in a terminally differentiated cartilage tissue. Primary cultures of human articular chondrocytes (ACs) and cartilage explants were set up from donor hip joint biopsies and were treated in vitro with PL. PL recruited a chondro-progenitors (CPCs)-enriched population from ex vivo cartilage culture, that showed high proliferation rate, clonogenicity and nestin expression. CPCs were positive for in vitro tri-lineage differentiation and formed hyaline cartilage-like tissue in vivo without hypertrophic fate. Moreover, the secretory profile of CPCs was analyzed, together with their migratory capabilities. Some CPC-features were also induced in PL-treated ACs compared to fetal bovine serum (FBS)-control ACs. PL treatment of human articular cartilage activates a stem cell niche responsive to injury. These facts can improve the PL therapeutic efficacy in cartilage applications. MDPI 2020-04-23 /pmc/articles/PMC7226425/ /pubmed/32340136 http://dx.doi.org/10.3390/cells9041052 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Carluccio, Simonetta
Martinelli, Daniela
Palamà, Maria Elisabetta Federica
Pereira, Rui Cruz
Benelli, Roberto
Guijarro, Ana
Cancedda, Ranieri
Gentili, Chiara
Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies
title Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies
title_full Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies
title_fullStr Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies
title_full_unstemmed Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies
title_short Progenitor Cells Activated by Platelet Lysate in Human Articular Cartilage as a Tool for Future Cartilage Engineering and Reparative Strategies
title_sort progenitor cells activated by platelet lysate in human articular cartilage as a tool for future cartilage engineering and reparative strategies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226425/
https://www.ncbi.nlm.nih.gov/pubmed/32340136
http://dx.doi.org/10.3390/cells9041052
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