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Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering

Because cartilage has limited regenerative capability, a fully efficient advanced therapy medicinal product is needed to treat severe cartilage damage. We evaluated a novel biomaterial obtained by decellularizing sturgeon chondral endoskeleton tissue for use in cartilage tissue engineering. In silic...

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Autores principales: Ortiz-Arrabal, Olimpia, Carmona, Ramón, García-García, Óscar-Darío, Chato-Astrain, Jesús, Sánchez-Porras, David, Domezain, Alberto, Oruezabal, Roke-Iñaki, Carriel, Víctor, Campos, Antonio, Alaminos, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301329/
https://www.ncbi.nlm.nih.gov/pubmed/34356839
http://dx.doi.org/10.3390/biomedicines9070775
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author Ortiz-Arrabal, Olimpia
Carmona, Ramón
García-García, Óscar-Darío
Chato-Astrain, Jesús
Sánchez-Porras, David
Domezain, Alberto
Oruezabal, Roke-Iñaki
Carriel, Víctor
Campos, Antonio
Alaminos, Miguel
author_facet Ortiz-Arrabal, Olimpia
Carmona, Ramón
García-García, Óscar-Darío
Chato-Astrain, Jesús
Sánchez-Porras, David
Domezain, Alberto
Oruezabal, Roke-Iñaki
Carriel, Víctor
Campos, Antonio
Alaminos, Miguel
author_sort Ortiz-Arrabal, Olimpia
collection PubMed
description Because cartilage has limited regenerative capability, a fully efficient advanced therapy medicinal product is needed to treat severe cartilage damage. We evaluated a novel biomaterial obtained by decellularizing sturgeon chondral endoskeleton tissue for use in cartilage tissue engineering. In silico analysis suggested high homology between human and sturgeon collagen proteins, and ultra-performance liquid chromatography confirmed that both types of cartilage consisted mainly of the same amino acids. Decellularized sturgeon cartilage was recellularized with human chondrocytes and four types of human mesenchymal stem cells (MSC) and their suitability for generating a cartilage substitute was assessed ex vivo and in vivo. The results supported the biocompatibility of the novel scaffold, as well as its ability to sustain cell adhesion, proliferation and differentiation. In vivo assays showed that the MSC cells in grafted cartilage disks were biosynthetically active and able to remodel the extracellular matrix of cartilage substitutes, with the production of type II collagen and other relevant components, especially when adipose tissue MSC were used. In addition, these cartilage substitutes triggered a pro-regenerative reaction mediated by CD206-positive M2 macrophages. These preliminary results warrant further research to characterize in greater detail the potential clinical translation of these novel cartilage substitutes.
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spelling pubmed-83013292021-07-24 Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering Ortiz-Arrabal, Olimpia Carmona, Ramón García-García, Óscar-Darío Chato-Astrain, Jesús Sánchez-Porras, David Domezain, Alberto Oruezabal, Roke-Iñaki Carriel, Víctor Campos, Antonio Alaminos, Miguel Biomedicines Article Because cartilage has limited regenerative capability, a fully efficient advanced therapy medicinal product is needed to treat severe cartilage damage. We evaluated a novel biomaterial obtained by decellularizing sturgeon chondral endoskeleton tissue for use in cartilage tissue engineering. In silico analysis suggested high homology between human and sturgeon collagen proteins, and ultra-performance liquid chromatography confirmed that both types of cartilage consisted mainly of the same amino acids. Decellularized sturgeon cartilage was recellularized with human chondrocytes and four types of human mesenchymal stem cells (MSC) and their suitability for generating a cartilage substitute was assessed ex vivo and in vivo. The results supported the biocompatibility of the novel scaffold, as well as its ability to sustain cell adhesion, proliferation and differentiation. In vivo assays showed that the MSC cells in grafted cartilage disks were biosynthetically active and able to remodel the extracellular matrix of cartilage substitutes, with the production of type II collagen and other relevant components, especially when adipose tissue MSC were used. In addition, these cartilage substitutes triggered a pro-regenerative reaction mediated by CD206-positive M2 macrophages. These preliminary results warrant further research to characterize in greater detail the potential clinical translation of these novel cartilage substitutes. MDPI 2021-07-04 /pmc/articles/PMC8301329/ /pubmed/34356839 http://dx.doi.org/10.3390/biomedicines9070775 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
Ortiz-Arrabal, Olimpia
Carmona, Ramón
García-García, Óscar-Darío
Chato-Astrain, Jesús
Sánchez-Porras, David
Domezain, Alberto
Oruezabal, Roke-Iñaki
Carriel, Víctor
Campos, Antonio
Alaminos, Miguel
Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering
title Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering
title_full Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering
title_fullStr Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering
title_full_unstemmed Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering
title_short Generation and Evaluation of Novel Biomaterials Based on Decellularized Sturgeon Cartilage for Use in Tissue Engineering
title_sort generation and evaluation of novel biomaterials based on decellularized sturgeon cartilage for use in tissue engineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301329/
https://www.ncbi.nlm.nih.gov/pubmed/34356839
http://dx.doi.org/10.3390/biomedicines9070775
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