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Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface

Current treatments for degenerative disc disease do not restore full biological functionality of the intervertebral disc (IVD). As a result, regenerative medicine approaches are being developed to generate a biological replacement that when implanted will restore form and function of the degenerated...

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Autores principales: Chong, Jasmine E., Santerre, J. Paul, Kandel, Rita A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323466/
https://www.ncbi.nlm.nih.gov/pubmed/32613164
http://dx.doi.org/10.1002/jsp2.1089
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author Chong, Jasmine E.
Santerre, J. Paul
Kandel, Rita A.
author_facet Chong, Jasmine E.
Santerre, J. Paul
Kandel, Rita A.
author_sort Chong, Jasmine E.
collection PubMed
description Current treatments for degenerative disc disease do not restore full biological functionality of the intervertebral disc (IVD). As a result, regenerative medicine approaches are being developed to generate a biological replacement that when implanted will restore form and function of the degenerated IVD. Tissue‐engineered models to date have focused on the generation of nucleus pulposus and annulus fibrosus IVD components. However, these tissues need to be integrated with a cartilage endplate in order for successful implantation to occur. The purpose of this study was to generate an in vitro annulus fibrosus‐cartilage interface model which would enable us to better understand the biological and biomechanical implications of such interfaces. It was hypothesized that in vitro‐formed outer annulus fibrosus (OAF) and cartilage tissues would integrate in direct‐contact coculture to yield an interface containing extracellular matrix with aspects resembling the native OAF‐CEP interface. In vitro‐formed tissues were generated using bovine OAF cell‐seeded angle‐ply, multi‐lamellated polycarbonate urethane scaffolds and articular chondrocytes, which were then placed in direct‐contact coculture. 2‐week old OAF tissues integrated with 3‐day old cartilage by 1 week of coculture. Immunohistochemical staining of 2‐week interfaces showed that distributions of collagen type I, collagen type II, and aggrecan were similar to the native bovine interface. The apparent tensile strength of the in vitro interface increased significantly between 2 and 4 weeks of coculture. In summary, an annulus fibrosus‐cartilage interface model can be formed in vitro which will facilitate the identification of conditions required to generate an entire tissue‐engineered disc replacement suitable for clinical use.
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spelling pubmed-73234662020-06-30 Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface Chong, Jasmine E. Santerre, J. Paul Kandel, Rita A. JOR Spine Research Articles Current treatments for degenerative disc disease do not restore full biological functionality of the intervertebral disc (IVD). As a result, regenerative medicine approaches are being developed to generate a biological replacement that when implanted will restore form and function of the degenerated IVD. Tissue‐engineered models to date have focused on the generation of nucleus pulposus and annulus fibrosus IVD components. However, these tissues need to be integrated with a cartilage endplate in order for successful implantation to occur. The purpose of this study was to generate an in vitro annulus fibrosus‐cartilage interface model which would enable us to better understand the biological and biomechanical implications of such interfaces. It was hypothesized that in vitro‐formed outer annulus fibrosus (OAF) and cartilage tissues would integrate in direct‐contact coculture to yield an interface containing extracellular matrix with aspects resembling the native OAF‐CEP interface. In vitro‐formed tissues were generated using bovine OAF cell‐seeded angle‐ply, multi‐lamellated polycarbonate urethane scaffolds and articular chondrocytes, which were then placed in direct‐contact coculture. 2‐week old OAF tissues integrated with 3‐day old cartilage by 1 week of coculture. Immunohistochemical staining of 2‐week interfaces showed that distributions of collagen type I, collagen type II, and aggrecan were similar to the native bovine interface. The apparent tensile strength of the in vitro interface increased significantly between 2 and 4 weeks of coculture. In summary, an annulus fibrosus‐cartilage interface model can be formed in vitro which will facilitate the identification of conditions required to generate an entire tissue‐engineered disc replacement suitable for clinical use. John Wiley & Sons, Inc. 2020-05-06 /pmc/articles/PMC7323466/ /pubmed/32613164 http://dx.doi.org/10.1002/jsp2.1089 Text en © 2020 The Authors. JOR Spine published by Wiley Periodicals, LLC on behalf of Orthopaedic Research Society JOR This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Chong, Jasmine E.
Santerre, J. Paul
Kandel, Rita A.
Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
title Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
title_full Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
title_fullStr Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
title_full_unstemmed Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
title_short Generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
title_sort generation of an in vitro model of the outer annulus fibrosus‐cartilage interface
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323466/
https://www.ncbi.nlm.nih.gov/pubmed/32613164
http://dx.doi.org/10.1002/jsp2.1089
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