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A scaffold-free approach to cartilage tissue generation using human embryonic stem cells
Articular cartilage functions as a shock absorber and facilitates the free movement of joints. Currently, there are no therapeutic drugs that promote the healing of damaged articular cartilage. Limitations associated with the two clinically relevant cell populations, human articular chondrocytes and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478992/ https://www.ncbi.nlm.nih.gov/pubmed/34584110 http://dx.doi.org/10.1038/s41598-021-97934-9 |
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author | Griffith, Lauren A. Arnold, Katherine M. Sengers, Bram G. Tare, Rahul S. Houghton, Franchesca D. |
author_facet | Griffith, Lauren A. Arnold, Katherine M. Sengers, Bram G. Tare, Rahul S. Houghton, Franchesca D. |
author_sort | Griffith, Lauren A. |
collection | PubMed |
description | Articular cartilage functions as a shock absorber and facilitates the free movement of joints. Currently, there are no therapeutic drugs that promote the healing of damaged articular cartilage. Limitations associated with the two clinically relevant cell populations, human articular chondrocytes and mesenchymal stem cells, necessitate finding an alternative cell source for cartilage repair. Human embryonic stem cells (hESCs) provide a readily accessible population of self-renewing, pluripotent cells with perceived immunoprivileged properties for cartilage generation. We have developed a robust method to generate 3D, scaffold-free, hyaline cartilage tissue constructs from hESCs that are composed of numerous chondrocytes in lacunae, embedded in an extracellular matrix containing Type II collagen, sulphated glycosaminoglycans and Aggrecan. The elastic (Young’s) modulus of the hESC-derived cartilage tissue constructs (0.91 ± 0.08 MPa) was comparable to full-thickness human articular cartilage (0.87 ± 0.09 MPa). Moreover, we have successfully scaled up the size of the scaffold-free, 3D hESC-derived cartilage tissue constructs to between 4.5 mm and 6 mm, thus enhancing their suitability for clinical application. |
format | Online Article Text |
id | pubmed-8478992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84789922021-09-30 A scaffold-free approach to cartilage tissue generation using human embryonic stem cells Griffith, Lauren A. Arnold, Katherine M. Sengers, Bram G. Tare, Rahul S. Houghton, Franchesca D. Sci Rep Article Articular cartilage functions as a shock absorber and facilitates the free movement of joints. Currently, there are no therapeutic drugs that promote the healing of damaged articular cartilage. Limitations associated with the two clinically relevant cell populations, human articular chondrocytes and mesenchymal stem cells, necessitate finding an alternative cell source for cartilage repair. Human embryonic stem cells (hESCs) provide a readily accessible population of self-renewing, pluripotent cells with perceived immunoprivileged properties for cartilage generation. We have developed a robust method to generate 3D, scaffold-free, hyaline cartilage tissue constructs from hESCs that are composed of numerous chondrocytes in lacunae, embedded in an extracellular matrix containing Type II collagen, sulphated glycosaminoglycans and Aggrecan. The elastic (Young’s) modulus of the hESC-derived cartilage tissue constructs (0.91 ± 0.08 MPa) was comparable to full-thickness human articular cartilage (0.87 ± 0.09 MPa). Moreover, we have successfully scaled up the size of the scaffold-free, 3D hESC-derived cartilage tissue constructs to between 4.5 mm and 6 mm, thus enhancing their suitability for clinical application. Nature Publishing Group UK 2021-09-28 /pmc/articles/PMC8478992/ /pubmed/34584110 http://dx.doi.org/10.1038/s41598-021-97934-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Griffith, Lauren A. Arnold, Katherine M. Sengers, Bram G. Tare, Rahul S. Houghton, Franchesca D. A scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
title | A scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
title_full | A scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
title_fullStr | A scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
title_full_unstemmed | A scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
title_short | A scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
title_sort | scaffold-free approach to cartilage tissue generation using human embryonic stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478992/ https://www.ncbi.nlm.nih.gov/pubmed/34584110 http://dx.doi.org/10.1038/s41598-021-97934-9 |
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