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In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty

Total disc replacement with an engineered substitute is a promising avenue for treating advanced intervertebral disc disease. Toward this goal, we developed cell-seeded disc-like angle ply structures (DAPS) and showed through in vitro studies that these constructs mature to match native disc composi...

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Autores principales: Martin, J. T., Gullbrand, S. E., Kim, D. H., Ikuta, K., Pfeifer, C. G., Ashinsky, B. G., Smith, L. J., Elliott, D. M., Smith, H. E., Mauck, R. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693867/
https://www.ncbi.nlm.nih.gov/pubmed/29150639
http://dx.doi.org/10.1038/s41598-017-15887-4
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author Martin, J. T.
Gullbrand, S. E.
Kim, D. H.
Ikuta, K.
Pfeifer, C. G.
Ashinsky, B. G.
Smith, L. J.
Elliott, D. M.
Smith, H. E.
Mauck, R. L.
author_facet Martin, J. T.
Gullbrand, S. E.
Kim, D. H.
Ikuta, K.
Pfeifer, C. G.
Ashinsky, B. G.
Smith, L. J.
Elliott, D. M.
Smith, H. E.
Mauck, R. L.
author_sort Martin, J. T.
collection PubMed
description Total disc replacement with an engineered substitute is a promising avenue for treating advanced intervertebral disc disease. Toward this goal, we developed cell-seeded disc-like angle ply structures (DAPS) and showed through in vitro studies that these constructs mature to match native disc composition, structure, and function with long-term culture. We then evaluated DAPS performance in an in vivo rat model of total disc replacement; over 5 weeks in vivo, DAPS maintained their structure, prevented intervertebral bony fusion, and matched native disc mechanical function at physiologic loads in situ. However, DAPS rapidly lost proteoglycan post-implantation and did not integrate into adjacent vertebrae. To address this, we modified the design to include polymer endplates to interface the DAPS with adjacent vertebrae, and showed that this modification mitigated in vivo proteoglycan loss while maintaining mechanical function and promoting integration. Together, these data demonstrate that cell-seeded engineered discs can replicate many characteristics of the native disc and are a viable option for total disc arthroplasty.
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spelling pubmed-56938672017-11-24 In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty Martin, J. T. Gullbrand, S. E. Kim, D. H. Ikuta, K. Pfeifer, C. G. Ashinsky, B. G. Smith, L. J. Elliott, D. M. Smith, H. E. Mauck, R. L. Sci Rep Article Total disc replacement with an engineered substitute is a promising avenue for treating advanced intervertebral disc disease. Toward this goal, we developed cell-seeded disc-like angle ply structures (DAPS) and showed through in vitro studies that these constructs mature to match native disc composition, structure, and function with long-term culture. We then evaluated DAPS performance in an in vivo rat model of total disc replacement; over 5 weeks in vivo, DAPS maintained their structure, prevented intervertebral bony fusion, and matched native disc mechanical function at physiologic loads in situ. However, DAPS rapidly lost proteoglycan post-implantation and did not integrate into adjacent vertebrae. To address this, we modified the design to include polymer endplates to interface the DAPS with adjacent vertebrae, and showed that this modification mitigated in vivo proteoglycan loss while maintaining mechanical function and promoting integration. Together, these data demonstrate that cell-seeded engineered discs can replicate many characteristics of the native disc and are a viable option for total disc arthroplasty. Nature Publishing Group UK 2017-11-17 /pmc/articles/PMC5693867/ /pubmed/29150639 http://dx.doi.org/10.1038/s41598-017-15887-4 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Martin, J. T.
Gullbrand, S. E.
Kim, D. H.
Ikuta, K.
Pfeifer, C. G.
Ashinsky, B. G.
Smith, L. J.
Elliott, D. M.
Smith, H. E.
Mauck, R. L.
In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty
title In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty
title_full In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty
title_fullStr In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty
title_full_unstemmed In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty
title_short In Vitro Maturation and In Vivo Integration and Function of an Engineered Cell-Seeded Disc-like Angle Ply Structure (DAPS) for Total Disc Arthroplasty
title_sort in vitro maturation and in vivo integration and function of an engineered cell-seeded disc-like angle ply structure (daps) for total disc arthroplasty
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693867/
https://www.ncbi.nlm.nih.gov/pubmed/29150639
http://dx.doi.org/10.1038/s41598-017-15887-4
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