Cargando…

Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model

Cartilage has poor regenerative capacity and thus damage to the joint surfaces presents a major clinical challenge. Recent research has focussed on the development of tissue-engineered and cell-based approaches for the treatment of cartilage and osteochondral injuries, with current clinically availa...

Descripción completa

Detalles Bibliográficos
Autores principales: Levingstone, Tanya J., Sheehy, Eamon J., Moran, Conor J., Cunniffe, Gráinne M., Diaz Payno, Pedro J., Brady, Robert T., Almeida, Henrique V., Carroll, Simon F., O’Byrne, John M., Kelly, Daniel J., Brama, Pieter AJ., O’ Brien, Fergal J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934472/
https://www.ncbi.nlm.nih.gov/pubmed/36824377
http://dx.doi.org/10.1016/j.bbiosy.2022.100066
_version_ 1784889894822215680
author Levingstone, Tanya J.
Sheehy, Eamon J.
Moran, Conor J.
Cunniffe, Gráinne M.
Diaz Payno, Pedro J.
Brady, Robert T.
Almeida, Henrique V.
Carroll, Simon F.
O’Byrne, John M.
Kelly, Daniel J.
Brama, Pieter AJ.
O’ Brien, Fergal J.
author_facet Levingstone, Tanya J.
Sheehy, Eamon J.
Moran, Conor J.
Cunniffe, Gráinne M.
Diaz Payno, Pedro J.
Brady, Robert T.
Almeida, Henrique V.
Carroll, Simon F.
O’Byrne, John M.
Kelly, Daniel J.
Brama, Pieter AJ.
O’ Brien, Fergal J.
author_sort Levingstone, Tanya J.
collection PubMed
description Cartilage has poor regenerative capacity and thus damage to the joint surfaces presents a major clinical challenge. Recent research has focussed on the development of tissue-engineered and cell-based approaches for the treatment of cartilage and osteochondral injuries, with current clinically available cell-based approaches including autologous chondrocyte implantation and matrix-assisted autologous chondrocyte implantation. However, these approaches have significant disadvantages due to the requirement for a two-stage surgical procedure and an in vitro chondrocyte expansion phase which increases logistical challenges, hospital times and costs. In this study, we hypothesized that seeding biomimetic tri-layered scaffolds, with proven regenerative potential, with chondrocyte/infrapatellar fat pad stromal cell co-cultures would improve their regenerative capacity compared to scaffolds implanted cell-free. Rapid cell isolation techniques, without the requirement for long term in vitro culture, were utilised to achieve co-cultures of chondrocytes and stromal cells and thus overcome the limitations of existing cell-based techniques. Cell-free and cell-seeded scaffolds were implanted in osteochondral defects, created within the femoral condyle and trochlear ridge, in a translational large animal goat model. While analysis showed trends towards delayed subchondral bone healing in the cell-seeded scaffold group, by the 12 month timepoint the cell-free and cell-seeded groups yield cartilage and bone tissue with comparable quality and quantity. The results of the study reinforce the potential of the biomimetic tri-layered scaffold to repair joint defects but failed to demonstrate a clear benefit from the addition of the CC/FPMSC co-culture to this scaffold. Taking into consideration the additional cost and complexity associated with the cell-seeded scaffold approach, this study demonstrates that the treatment of osteochondral defects using cell-free tri-layered scaffolds may represent a more prudent clinical approach.
format Online
Article
Text
id pubmed-9934472
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-99344722023-02-22 Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model Levingstone, Tanya J. Sheehy, Eamon J. Moran, Conor J. Cunniffe, Gráinne M. Diaz Payno, Pedro J. Brady, Robert T. Almeida, Henrique V. Carroll, Simon F. O’Byrne, John M. Kelly, Daniel J. Brama, Pieter AJ. O’ Brien, Fergal J. Biomater Biosyst Research Article Cartilage has poor regenerative capacity and thus damage to the joint surfaces presents a major clinical challenge. Recent research has focussed on the development of tissue-engineered and cell-based approaches for the treatment of cartilage and osteochondral injuries, with current clinically available cell-based approaches including autologous chondrocyte implantation and matrix-assisted autologous chondrocyte implantation. However, these approaches have significant disadvantages due to the requirement for a two-stage surgical procedure and an in vitro chondrocyte expansion phase which increases logistical challenges, hospital times and costs. In this study, we hypothesized that seeding biomimetic tri-layered scaffolds, with proven regenerative potential, with chondrocyte/infrapatellar fat pad stromal cell co-cultures would improve their regenerative capacity compared to scaffolds implanted cell-free. Rapid cell isolation techniques, without the requirement for long term in vitro culture, were utilised to achieve co-cultures of chondrocytes and stromal cells and thus overcome the limitations of existing cell-based techniques. Cell-free and cell-seeded scaffolds were implanted in osteochondral defects, created within the femoral condyle and trochlear ridge, in a translational large animal goat model. While analysis showed trends towards delayed subchondral bone healing in the cell-seeded scaffold group, by the 12 month timepoint the cell-free and cell-seeded groups yield cartilage and bone tissue with comparable quality and quantity. The results of the study reinforce the potential of the biomimetic tri-layered scaffold to repair joint defects but failed to demonstrate a clear benefit from the addition of the CC/FPMSC co-culture to this scaffold. Taking into consideration the additional cost and complexity associated with the cell-seeded scaffold approach, this study demonstrates that the treatment of osteochondral defects using cell-free tri-layered scaffolds may represent a more prudent clinical approach. Elsevier 2022-10-08 /pmc/articles/PMC9934472/ /pubmed/36824377 http://dx.doi.org/10.1016/j.bbiosy.2022.100066 Text en © 2022 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Levingstone, Tanya J.
Sheehy, Eamon J.
Moran, Conor J.
Cunniffe, Gráinne M.
Diaz Payno, Pedro J.
Brady, Robert T.
Almeida, Henrique V.
Carroll, Simon F.
O’Byrne, John M.
Kelly, Daniel J.
Brama, Pieter AJ.
O’ Brien, Fergal J.
Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
title Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
title_full Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
title_fullStr Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
title_full_unstemmed Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
title_short Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
title_sort evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934472/
https://www.ncbi.nlm.nih.gov/pubmed/36824377
http://dx.doi.org/10.1016/j.bbiosy.2022.100066
work_keys_str_mv AT levingstonetanyaj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT sheehyeamonj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT moranconorj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT cunniffegrainnem evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT diazpaynopedroj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT bradyrobertt evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT almeidahenriquev evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT carrollsimonf evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT obyrnejohnm evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT kellydanielj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT bramapieteraj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel
AT obrienfergalj evaluationofacocultureofrapidlyisolatedchondrocytesandstemcellsseededontrilayeredcollagenbasedscaffoldsinacaprineosteochondraldefectmodel