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Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells
We have created entirely biological tissue-engineered vascular grafts (TEVGs) using sheets of cell-assembled extracellular matrix (CAM) produced by human fibroblasts in vitro. A large animal TEVG would allow long-term pre-clinical studies in a clinically relevant setting (graft size and allogeneic s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887678/ https://www.ncbi.nlm.nih.gov/pubmed/33633827 http://dx.doi.org/10.1177/2041731420978327 |
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author | Torres, Yoann Gluais, Maude Da Silva, Nicolas Rey, Sylvie Grémare, Agathe Magnan, Laure Kawecki, Fabien L’Heureux, Nicolas |
author_facet | Torres, Yoann Gluais, Maude Da Silva, Nicolas Rey, Sylvie Grémare, Agathe Magnan, Laure Kawecki, Fabien L’Heureux, Nicolas |
author_sort | Torres, Yoann |
collection | PubMed |
description | We have created entirely biological tissue-engineered vascular grafts (TEVGs) using sheets of cell-assembled extracellular matrix (CAM) produced by human fibroblasts in vitro. A large animal TEVG would allow long-term pre-clinical studies in a clinically relevant setting (graft size and allogeneic setting). Therefore, canine, porcine, ovine, and human skin fibroblasts were compared for their ability to form CAM sheets. Serum sourcing greatly influenced CAM production in a species-dependent manner. Ovine cells produced the most homogenous and strongest animal CAM sheets but remained ≈3-fold weaker than human sheets despite variations of serum, ascorbate, insulin, or growth factor supplementations. Key differences in cell growth dynamics, tissue development, and tissue architecture and composition were observed between human and ovine. This study demonstrates critical species-to-species differences in fibroblast behavior and how they pose a challenge when attempting to substitute animal cells for human cells during the development of tissue-engineered constructs that require long-term cultures. |
format | Online Article Text |
id | pubmed-7887678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78876782021-02-24 Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells Torres, Yoann Gluais, Maude Da Silva, Nicolas Rey, Sylvie Grémare, Agathe Magnan, Laure Kawecki, Fabien L’Heureux, Nicolas J Tissue Eng Original Article We have created entirely biological tissue-engineered vascular grafts (TEVGs) using sheets of cell-assembled extracellular matrix (CAM) produced by human fibroblasts in vitro. A large animal TEVG would allow long-term pre-clinical studies in a clinically relevant setting (graft size and allogeneic setting). Therefore, canine, porcine, ovine, and human skin fibroblasts were compared for their ability to form CAM sheets. Serum sourcing greatly influenced CAM production in a species-dependent manner. Ovine cells produced the most homogenous and strongest animal CAM sheets but remained ≈3-fold weaker than human sheets despite variations of serum, ascorbate, insulin, or growth factor supplementations. Key differences in cell growth dynamics, tissue development, and tissue architecture and composition were observed between human and ovine. This study demonstrates critical species-to-species differences in fibroblast behavior and how they pose a challenge when attempting to substitute animal cells for human cells during the development of tissue-engineered constructs that require long-term cultures. SAGE Publications 2021-02-12 /pmc/articles/PMC7887678/ /pubmed/33633827 http://dx.doi.org/10.1177/2041731420978327 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Torres, Yoann Gluais, Maude Da Silva, Nicolas Rey, Sylvie Grémare, Agathe Magnan, Laure Kawecki, Fabien L’Heureux, Nicolas Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells |
title | Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells |
title_full | Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells |
title_fullStr | Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells |
title_full_unstemmed | Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells |
title_short | Cell-assembled extracellular matrix (CAM) sheet production: Translation from using human to large animal cells |
title_sort | cell-assembled extracellular matrix (cam) sheet production: translation from using human to large animal cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887678/ https://www.ncbi.nlm.nih.gov/pubmed/33633827 http://dx.doi.org/10.1177/2041731420978327 |
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