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3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation
Human articular cartilage is highly susceptible to damage and has limited self-repair and regeneration potential. Cell-based strategies to engineer cartilage tissue offer a promising solution to repair articular cartilage. To select the optimal cell source for tissue repair, it is important to devel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692641/ https://www.ncbi.nlm.nih.gov/pubmed/26484414 http://dx.doi.org/10.3791/53085 |
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author | Smeriglio, Piera Lai, Janice H. Yang, Fan Bhutani, Nidhi |
author_facet | Smeriglio, Piera Lai, Janice H. Yang, Fan Bhutani, Nidhi |
author_sort | Smeriglio, Piera |
collection | PubMed |
description | Human articular cartilage is highly susceptible to damage and has limited self-repair and regeneration potential. Cell-based strategies to engineer cartilage tissue offer a promising solution to repair articular cartilage. To select the optimal cell source for tissue repair, it is important to develop an appropriate culture platform to systematically examine the biological and biomechanical differences in the tissue-engineered cartilage by different cell sources. Here we applied a three-dimensional (3D) biomimetic hydrogel culture platform to systematically examine cartilage regeneration potential of juvenile, adult, and osteoarthritic (OA) chondrocytes. The 3D biomimetic hydrogel consisted of synthetic component poly(ethylene glycol) and bioactive component chondroitin sulfate, which provides a physiologically relevant microenvironment for in vitro culture of chondrocytes. In addition, the scaffold may be potentially used for cell delivery for cartilage repair in vivo. Cartilage tissue engineered in the scaffold can be evaluated using quantitative gene expression, immunofluorescence staining, biochemical assays, and mechanical testing. Utilizing these outcomes, we were able to characterize the differential regenerative potential of chondrocytes of varying age, both at the gene expression level and in the biochemical and biomechanical properties of the engineered cartilage tissue. The 3D culture model could be applied to investigate the molecular and functional differences among chondrocytes and progenitor cells from different stages of normal or aberrant development. |
format | Online Article Text |
id | pubmed-4692641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-46926412016-01-07 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation Smeriglio, Piera Lai, Janice H. Yang, Fan Bhutani, Nidhi J Vis Exp Bioengineering Human articular cartilage is highly susceptible to damage and has limited self-repair and regeneration potential. Cell-based strategies to engineer cartilage tissue offer a promising solution to repair articular cartilage. To select the optimal cell source for tissue repair, it is important to develop an appropriate culture platform to systematically examine the biological and biomechanical differences in the tissue-engineered cartilage by different cell sources. Here we applied a three-dimensional (3D) biomimetic hydrogel culture platform to systematically examine cartilage regeneration potential of juvenile, adult, and osteoarthritic (OA) chondrocytes. The 3D biomimetic hydrogel consisted of synthetic component poly(ethylene glycol) and bioactive component chondroitin sulfate, which provides a physiologically relevant microenvironment for in vitro culture of chondrocytes. In addition, the scaffold may be potentially used for cell delivery for cartilage repair in vivo. Cartilage tissue engineered in the scaffold can be evaluated using quantitative gene expression, immunofluorescence staining, biochemical assays, and mechanical testing. Utilizing these outcomes, we were able to characterize the differential regenerative potential of chondrocytes of varying age, both at the gene expression level and in the biochemical and biomechanical properties of the engineered cartilage tissue. The 3D culture model could be applied to investigate the molecular and functional differences among chondrocytes and progenitor cells from different stages of normal or aberrant development. MyJove Corporation 2015-10-07 /pmc/articles/PMC4692641/ /pubmed/26484414 http://dx.doi.org/10.3791/53085 Text en Copyright © 2015, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Bioengineering Smeriglio, Piera Lai, Janice H. Yang, Fan Bhutani, Nidhi 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation |
title | 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation |
title_full | 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation |
title_fullStr | 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation |
title_full_unstemmed | 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation |
title_short | 3D Hydrogel Scaffolds for Articular Chondrocyte Culture and Cartilage Generation |
title_sort | 3d hydrogel scaffolds for articular chondrocyte culture and cartilage generation |
topic | Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692641/ https://www.ncbi.nlm.nih.gov/pubmed/26484414 http://dx.doi.org/10.3791/53085 |
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