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Induction of cartilage integration by a chondrocyte/collagen-scaffold implant

The integration of implanted cartilage is a major challenge for the success of tissue engineering protocols. We hypothesize that in order for effective cartilage integration to take place, matrix-free chondrocytes must be induced to migrate between the two tissue surfaces. A chondrocyte/collagen-sca...

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Autores principales: Pabbruwe, Moreica B., Esfandiari, Ehsanollah, Kafienah, Wael, Tarlton, John F., Hollander, Anthony P.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723758/
https://www.ncbi.nlm.nih.gov/pubmed/19539365
http://dx.doi.org/10.1016/j.biomaterials.2009.02.052
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author Pabbruwe, Moreica B.
Esfandiari, Ehsanollah
Kafienah, Wael
Tarlton, John F.
Hollander, Anthony P.
author_facet Pabbruwe, Moreica B.
Esfandiari, Ehsanollah
Kafienah, Wael
Tarlton, John F.
Hollander, Anthony P.
author_sort Pabbruwe, Moreica B.
collection PubMed
description The integration of implanted cartilage is a major challenge for the success of tissue engineering protocols. We hypothesize that in order for effective cartilage integration to take place, matrix-free chondrocytes must be induced to migrate between the two tissue surfaces. A chondrocyte/collagen-scaffold implant system was developed as a method of delivering dividing cells at the interface between two cartilage surfaces. Chondrocytes were isolated from bovine nasal septum and seeded onto both surfaces of a collagen membrane to create the chondrocyte/collagen-scaffold implant. A model of two cartilage discs and the chondrocyte/collagen-scaffold sandwiched in between was used to effect integration in vitro. The resulting tissue was analysed histologically and biomechanically. The cartilage–implant–cartilage sandwich appeared macroscopically as one continuous piece of tissue at the end of 40 day cultures. Histological analysis showed tissue continuum across the cartilage–scaffold interface. The integration was dependent on both cells and scaffold. Fluorescent labeling of implanted chondrocytes demonstrated that these cells invade the surrounding mature tissue and drive a remodelling of the extracellular matrix. Using cell-free scaffolds we also demonstrated that some chondrocytes migrated from the natural cartilage into the collagen scaffold. Quantification of integration levels using a histomorphometric repair index showed that the chondrocyte/collagen-scaffold implant achieved the highest repair index compared to controls, reflected functionally through increased tensile strength. In conclusion, cartilage integration can be achieved using a chondrocyte/collagen-scaffold implant that permits controlled delivery of chondrocytes to both host and graft mature cartilage tissues. This approach has the potential to be used therapeutically for implantation of engineered tissue.
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spelling pubmed-27237582009-08-18 Induction of cartilage integration by a chondrocyte/collagen-scaffold implant Pabbruwe, Moreica B. Esfandiari, Ehsanollah Kafienah, Wael Tarlton, John F. Hollander, Anthony P. Biomaterials Article The integration of implanted cartilage is a major challenge for the success of tissue engineering protocols. We hypothesize that in order for effective cartilage integration to take place, matrix-free chondrocytes must be induced to migrate between the two tissue surfaces. A chondrocyte/collagen-scaffold implant system was developed as a method of delivering dividing cells at the interface between two cartilage surfaces. Chondrocytes were isolated from bovine nasal septum and seeded onto both surfaces of a collagen membrane to create the chondrocyte/collagen-scaffold implant. A model of two cartilage discs and the chondrocyte/collagen-scaffold sandwiched in between was used to effect integration in vitro. The resulting tissue was analysed histologically and biomechanically. The cartilage–implant–cartilage sandwich appeared macroscopically as one continuous piece of tissue at the end of 40 day cultures. Histological analysis showed tissue continuum across the cartilage–scaffold interface. The integration was dependent on both cells and scaffold. Fluorescent labeling of implanted chondrocytes demonstrated that these cells invade the surrounding mature tissue and drive a remodelling of the extracellular matrix. Using cell-free scaffolds we also demonstrated that some chondrocytes migrated from the natural cartilage into the collagen scaffold. Quantification of integration levels using a histomorphometric repair index showed that the chondrocyte/collagen-scaffold implant achieved the highest repair index compared to controls, reflected functionally through increased tensile strength. In conclusion, cartilage integration can be achieved using a chondrocyte/collagen-scaffold implant that permits controlled delivery of chondrocytes to both host and graft mature cartilage tissues. This approach has the potential to be used therapeutically for implantation of engineered tissue. Elsevier Science 2009-09 /pmc/articles/PMC2723758/ /pubmed/19539365 http://dx.doi.org/10.1016/j.biomaterials.2009.02.052 Text en © 2009 Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Pabbruwe, Moreica B.
Esfandiari, Ehsanollah
Kafienah, Wael
Tarlton, John F.
Hollander, Anthony P.
Induction of cartilage integration by a chondrocyte/collagen-scaffold implant
title Induction of cartilage integration by a chondrocyte/collagen-scaffold implant
title_full Induction of cartilage integration by a chondrocyte/collagen-scaffold implant
title_fullStr Induction of cartilage integration by a chondrocyte/collagen-scaffold implant
title_full_unstemmed Induction of cartilage integration by a chondrocyte/collagen-scaffold implant
title_short Induction of cartilage integration by a chondrocyte/collagen-scaffold implant
title_sort induction of cartilage integration by a chondrocyte/collagen-scaffold implant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723758/
https://www.ncbi.nlm.nih.gov/pubmed/19539365
http://dx.doi.org/10.1016/j.biomaterials.2009.02.052
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