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Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle
Tissue engineered skeletal muscle allows investigation of the cellular and molecular mechanisms that regulate skeletal muscle pathology. The fabricated model must resemble characteristics of in vivo tissue and incorporate cost-effective and high content primary human tissue. Current models are limit...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383409/ https://www.ncbi.nlm.nih.gov/pubmed/30838203 http://dx.doi.org/10.3389/fbioe.2019.00020 |
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author | Capel, Andrew J. Rimington, Rowan P. Fleming, Jacob W. Player, Darren J. Baker, Luke A. Turner, Mark C. Jones, Julia M. Martin, Neil R. W. Ferguson, Richard A. Mudera, Vivek C. Lewis, Mark P. |
author_facet | Capel, Andrew J. Rimington, Rowan P. Fleming, Jacob W. Player, Darren J. Baker, Luke A. Turner, Mark C. Jones, Julia M. Martin, Neil R. W. Ferguson, Richard A. Mudera, Vivek C. Lewis, Mark P. |
author_sort | Capel, Andrew J. |
collection | PubMed |
description | Tissue engineered skeletal muscle allows investigation of the cellular and molecular mechanisms that regulate skeletal muscle pathology. The fabricated model must resemble characteristics of in vivo tissue and incorporate cost-effective and high content primary human tissue. Current models are limited by low throughput due to the complexities associated with recruiting tissue donors, donor specific variations, as well as cellular senescence associated with passaging. This research presents a method using fused deposition modeling (FDM) and laser sintering (LS) 3D printing to generate reproducible and scalable tissue engineered primary human muscle, possessing aligned mature myotubes reminiscent of in vivo tissue. Many existing models are bespoke causing variability when translated between laboratories. To this end, a scalable model has been developed (25–500 μL construct volumes) allowing fabrication of mature primary human skeletal muscle. This research provides a strategy to overcome limited biopsy cell numbers, enabling high throughput screening of functional human tissue. |
format | Online Article Text |
id | pubmed-6383409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63834092019-03-05 Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle Capel, Andrew J. Rimington, Rowan P. Fleming, Jacob W. Player, Darren J. Baker, Luke A. Turner, Mark C. Jones, Julia M. Martin, Neil R. W. Ferguson, Richard A. Mudera, Vivek C. Lewis, Mark P. Front Bioeng Biotechnol Bioengineering and Biotechnology Tissue engineered skeletal muscle allows investigation of the cellular and molecular mechanisms that regulate skeletal muscle pathology. The fabricated model must resemble characteristics of in vivo tissue and incorporate cost-effective and high content primary human tissue. Current models are limited by low throughput due to the complexities associated with recruiting tissue donors, donor specific variations, as well as cellular senescence associated with passaging. This research presents a method using fused deposition modeling (FDM) and laser sintering (LS) 3D printing to generate reproducible and scalable tissue engineered primary human muscle, possessing aligned mature myotubes reminiscent of in vivo tissue. Many existing models are bespoke causing variability when translated between laboratories. To this end, a scalable model has been developed (25–500 μL construct volumes) allowing fabrication of mature primary human skeletal muscle. This research provides a strategy to overcome limited biopsy cell numbers, enabling high throughput screening of functional human tissue. Frontiers Media S.A. 2019-02-14 /pmc/articles/PMC6383409/ /pubmed/30838203 http://dx.doi.org/10.3389/fbioe.2019.00020 Text en Copyright © 2019 Capel, Rimington, Fleming, Player, Baker, Turner, Jones, Martin, Ferguson, Mudera and Lewis. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Capel, Andrew J. Rimington, Rowan P. Fleming, Jacob W. Player, Darren J. Baker, Luke A. Turner, Mark C. Jones, Julia M. Martin, Neil R. W. Ferguson, Richard A. Mudera, Vivek C. Lewis, Mark P. Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle |
title | Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle |
title_full | Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle |
title_fullStr | Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle |
title_full_unstemmed | Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle |
title_short | Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle |
title_sort | scalable 3d printed molds for human tissue engineered skeletal muscle |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383409/ https://www.ncbi.nlm.nih.gov/pubmed/30838203 http://dx.doi.org/10.3389/fbioe.2019.00020 |
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