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Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration
The transition areas between different tissues, known as tissue interfaces, have limited ability to regenerate after damage, which can lead to incomplete healing. Previous studies focussed on single interfaces, most commonly bone-tendon and bone-cartilage interfaces. Herein, we develop a 3D in vitro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856925/ https://www.ncbi.nlm.nih.gov/pubmed/36672248 http://dx.doi.org/10.3390/cells12020313 |
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author | Balestri, Wendy Hickman, Graham J. Morris, Robert H. Hunt, John A. Reinwald, Yvonne |
author_facet | Balestri, Wendy Hickman, Graham J. Morris, Robert H. Hunt, John A. Reinwald, Yvonne |
author_sort | Balestri, Wendy |
collection | PubMed |
description | The transition areas between different tissues, known as tissue interfaces, have limited ability to regenerate after damage, which can lead to incomplete healing. Previous studies focussed on single interfaces, most commonly bone-tendon and bone-cartilage interfaces. Herein, we develop a 3D in vitro model to study the regeneration of the bone-tendon-muscle interface. The 3D model was prepared from collagen and agarose, with different concentrations of hydroxyapatite to graduate the tissues from bones to muscles, resulting in a stiffness gradient. This graduated structure was fabricated using indirect 3D printing to provide biologically relevant surface topographies. MG-63, human dermal fibroblasts, and Sket.4U cells were found suitable cell models for bones, tendons, and muscles, respectively. The biphasic and triphasic hydrogels composing the 3D model were shown to be suitable for cell growth. Cells were co-cultured on the 3D model for over 21 days before assessing cell proliferation, metabolic activity, viability, cytotoxicity, tissue-specific markers, and matrix deposition to determine interface formations. The studies were conducted in a newly developed growth chamber that allowed cell communication while the cell culture media was compartmentalised. The 3D model promoted cell viability, tissue-specific marker expression, and new matrix deposition over 21 days, thereby showing promise for the development of new interfaces. |
format | Online Article Text |
id | pubmed-9856925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98569252023-01-21 Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration Balestri, Wendy Hickman, Graham J. Morris, Robert H. Hunt, John A. Reinwald, Yvonne Cells Article The transition areas between different tissues, known as tissue interfaces, have limited ability to regenerate after damage, which can lead to incomplete healing. Previous studies focussed on single interfaces, most commonly bone-tendon and bone-cartilage interfaces. Herein, we develop a 3D in vitro model to study the regeneration of the bone-tendon-muscle interface. The 3D model was prepared from collagen and agarose, with different concentrations of hydroxyapatite to graduate the tissues from bones to muscles, resulting in a stiffness gradient. This graduated structure was fabricated using indirect 3D printing to provide biologically relevant surface topographies. MG-63, human dermal fibroblasts, and Sket.4U cells were found suitable cell models for bones, tendons, and muscles, respectively. The biphasic and triphasic hydrogels composing the 3D model were shown to be suitable for cell growth. Cells were co-cultured on the 3D model for over 21 days before assessing cell proliferation, metabolic activity, viability, cytotoxicity, tissue-specific markers, and matrix deposition to determine interface formations. The studies were conducted in a newly developed growth chamber that allowed cell communication while the cell culture media was compartmentalised. The 3D model promoted cell viability, tissue-specific marker expression, and new matrix deposition over 21 days, thereby showing promise for the development of new interfaces. MDPI 2023-01-13 /pmc/articles/PMC9856925/ /pubmed/36672248 http://dx.doi.org/10.3390/cells12020313 Text en © 2023 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 Balestri, Wendy Hickman, Graham J. Morris, Robert H. Hunt, John A. Reinwald, Yvonne Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration |
title | Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration |
title_full | Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration |
title_fullStr | Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration |
title_full_unstemmed | Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration |
title_short | Triphasic 3D In Vitro Model of Bone-Tendon-Muscle Interfaces to Study Their Regeneration |
title_sort | triphasic 3d in vitro model of bone-tendon-muscle interfaces to study their regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856925/ https://www.ncbi.nlm.nih.gov/pubmed/36672248 http://dx.doi.org/10.3390/cells12020313 |
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