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Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study

Matrix-assisted autologous chondrocyte implantation (MACI) has shown promising results for cartilage repair, combining cultured chondrocytes and hydrogels, including alginate. The ability of chondrocytes for MACI is limited by different factors including donor site morbidity, dedifferentiation, limi...

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Autores principales: Oliver-Ferrándiz, María, Milián, Lara, Sancho-Tello, María, Martín de Llano, José Javier, Gisbert Roca, Fernando, Martínez-Ramos, Cristina, Carda, Carmen, Mata, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301309/
https://www.ncbi.nlm.nih.gov/pubmed/34356898
http://dx.doi.org/10.3390/biomedicines9070834
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author Oliver-Ferrándiz, María
Milián, Lara
Sancho-Tello, María
Martín de Llano, José Javier
Gisbert Roca, Fernando
Martínez-Ramos, Cristina
Carda, Carmen
Mata, Manuel
author_facet Oliver-Ferrándiz, María
Milián, Lara
Sancho-Tello, María
Martín de Llano, José Javier
Gisbert Roca, Fernando
Martínez-Ramos, Cristina
Carda, Carmen
Mata, Manuel
author_sort Oliver-Ferrándiz, María
collection PubMed
description Matrix-assisted autologous chondrocyte implantation (MACI) has shown promising results for cartilage repair, combining cultured chondrocytes and hydrogels, including alginate. The ability of chondrocytes for MACI is limited by different factors including donor site morbidity, dedifferentiation, limited lifespan or poor proliferation in vitro. Mesenchymal stem cells could represent an alternative for cartilage regeneration. In this study, we propose a MACI scaffold consisting of a mixed alginate-agarose hydrogel in combination with human dental pulp stem cells (hDPSCs), suitable for cartilage regeneration. Scaffolds were characterized according to their rheological properties, and their histomorphometric and molecular biology results. Agarose significantly improved the biomechanical behavior of the alginate scaffolds. Large scaffolds were manufactured, and a homogeneous distribution of cells was observed within them. Although primary chondrocytes showed a greater capacity for chondrogenic differentiation, hDPSCs cultured in the scaffolds formed large aggregates of cells, acquired a rounded morphology and expressed high amounts of type II collagen and aggrecan. Cells cultured in the scaffolds expressed not only chondral matrix-related genes, but also remodeling proteins and chondrocyte differentiation factors. The degree of differentiation of cells was proportional to the number and size of the cell aggregates that were formed in the hydrogels.
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spelling pubmed-83013092021-07-24 Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study Oliver-Ferrándiz, María Milián, Lara Sancho-Tello, María Martín de Llano, José Javier Gisbert Roca, Fernando Martínez-Ramos, Cristina Carda, Carmen Mata, Manuel Biomedicines Article Matrix-assisted autologous chondrocyte implantation (MACI) has shown promising results for cartilage repair, combining cultured chondrocytes and hydrogels, including alginate. The ability of chondrocytes for MACI is limited by different factors including donor site morbidity, dedifferentiation, limited lifespan or poor proliferation in vitro. Mesenchymal stem cells could represent an alternative for cartilage regeneration. In this study, we propose a MACI scaffold consisting of a mixed alginate-agarose hydrogel in combination with human dental pulp stem cells (hDPSCs), suitable for cartilage regeneration. Scaffolds were characterized according to their rheological properties, and their histomorphometric and molecular biology results. Agarose significantly improved the biomechanical behavior of the alginate scaffolds. Large scaffolds were manufactured, and a homogeneous distribution of cells was observed within them. Although primary chondrocytes showed a greater capacity for chondrogenic differentiation, hDPSCs cultured in the scaffolds formed large aggregates of cells, acquired a rounded morphology and expressed high amounts of type II collagen and aggrecan. Cells cultured in the scaffolds expressed not only chondral matrix-related genes, but also remodeling proteins and chondrocyte differentiation factors. The degree of differentiation of cells was proportional to the number and size of the cell aggregates that were formed in the hydrogels. MDPI 2021-07-17 /pmc/articles/PMC8301309/ /pubmed/34356898 http://dx.doi.org/10.3390/biomedicines9070834 Text en © 2021 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
Oliver-Ferrándiz, María
Milián, Lara
Sancho-Tello, María
Martín de Llano, José Javier
Gisbert Roca, Fernando
Martínez-Ramos, Cristina
Carda, Carmen
Mata, Manuel
Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study
title Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study
title_full Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study
title_fullStr Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study
title_full_unstemmed Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study
title_short Alginate-Agarose Hydrogels Improve the In Vitro Differentiation of Human Dental Pulp Stem Cells in Chondrocytes. A Histological Study
title_sort alginate-agarose hydrogels improve the in vitro differentiation of human dental pulp stem cells in chondrocytes. a histological study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301309/
https://www.ncbi.nlm.nih.gov/pubmed/34356898
http://dx.doi.org/10.3390/biomedicines9070834
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