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Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation

OBJECTIVE: Early surgical intervention for articular cartilage disease is desirable before full-thickness lesions develop. As early intervention treatments are designed, native chondrocyte viability at the treatment site before intervention becomes an important parameter to consider. The purpose of...

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Detalles Bibliográficos
Autores principales: Ganguly, Kumkum, McRury, Ian D., Goodwin, Peter M., Morgan, Roy E., Augé, Wayne K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297056/
https://www.ncbi.nlm.nih.gov/pubmed/26069561
http://dx.doi.org/10.1177/1947603510373918
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author Ganguly, Kumkum
McRury, Ian D.
Goodwin, Peter M.
Morgan, Roy E.
Augé, Wayne K.
author_facet Ganguly, Kumkum
McRury, Ian D.
Goodwin, Peter M.
Morgan, Roy E.
Augé, Wayne K.
author_sort Ganguly, Kumkum
collection PubMed
description OBJECTIVE: Early surgical intervention for articular cartilage disease is desirable before full-thickness lesions develop. As early intervention treatments are designed, native chondrocyte viability at the treatment site before intervention becomes an important parameter to consider. The purpose of this study is to evaluate native chondrocyte viability in a series of specimens demonstrating the progression of articular cartilage lesions to determine if the chondrocyte viability profile changes during the evolution of articular cartilage disease to the level of surface fibrillation. DESIGN: Osteochondral specimens demonstrating various degrees of articular cartilage damage were obtained from patients undergoing knee total joint replacement. Three groups were created within a patient harvest based on visual and tactile cues commonly encountered during surgical intervention: group 1, visually and tactilely intact surfaces; group 2, visually intact, tactilely soft surfaces; and group 3, surface fibrillation. Confocal laser microscopy was performed following live/dead cell viability staining. RESULTS: Groups 1 to 3 demonstrated viable chondrocytes in all specimens, even within the fibrillated portions of articular cartilage, with little to no evidence of dead chondrocytes. Chondrocyte viability profile in articular cartilage does not appear to change as disease lesion progresses from normal to surface fibrillation. CONCLUSIONS: Fibrillated partial-thickness articular cartilage lesions are a good therapeutic target for early intervention. These lesions retain a high profile of viable chondrocytes and are readily diagnosed by visual and tactile cues during surgery. Early intervention should be based on matrix failure rather than on more aggressive procedures that further corrupt the matrix and contribute to chondrocyte necrosis of contiguous untargeted cartilage.
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spelling pubmed-42970562015-06-11 Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation Ganguly, Kumkum McRury, Ian D. Goodwin, Peter M. Morgan, Roy E. Augé, Wayne K. Cartilage Original Articles OBJECTIVE: Early surgical intervention for articular cartilage disease is desirable before full-thickness lesions develop. As early intervention treatments are designed, native chondrocyte viability at the treatment site before intervention becomes an important parameter to consider. The purpose of this study is to evaluate native chondrocyte viability in a series of specimens demonstrating the progression of articular cartilage lesions to determine if the chondrocyte viability profile changes during the evolution of articular cartilage disease to the level of surface fibrillation. DESIGN: Osteochondral specimens demonstrating various degrees of articular cartilage damage were obtained from patients undergoing knee total joint replacement. Three groups were created within a patient harvest based on visual and tactile cues commonly encountered during surgical intervention: group 1, visually and tactilely intact surfaces; group 2, visually intact, tactilely soft surfaces; and group 3, surface fibrillation. Confocal laser microscopy was performed following live/dead cell viability staining. RESULTS: Groups 1 to 3 demonstrated viable chondrocytes in all specimens, even within the fibrillated portions of articular cartilage, with little to no evidence of dead chondrocytes. Chondrocyte viability profile in articular cartilage does not appear to change as disease lesion progresses from normal to surface fibrillation. CONCLUSIONS: Fibrillated partial-thickness articular cartilage lesions are a good therapeutic target for early intervention. These lesions retain a high profile of viable chondrocytes and are readily diagnosed by visual and tactile cues during surgery. Early intervention should be based on matrix failure rather than on more aggressive procedures that further corrupt the matrix and contribute to chondrocyte necrosis of contiguous untargeted cartilage. SAGE Publications 2010-10 /pmc/articles/PMC4297056/ /pubmed/26069561 http://dx.doi.org/10.1177/1947603510373918 Text en © The Author(s) 2010
spellingShingle Original Articles
Ganguly, Kumkum
McRury, Ian D.
Goodwin, Peter M.
Morgan, Roy E.
Augé, Wayne K.
Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation
title Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation
title_full Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation
title_fullStr Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation
title_full_unstemmed Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation
title_short Native Chondrocyte Viability during Cartilage Lesion Progression: Normal to Surface Fibrillation
title_sort native chondrocyte viability during cartilage lesion progression: normal to surface fibrillation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297056/
https://www.ncbi.nlm.nih.gov/pubmed/26069561
http://dx.doi.org/10.1177/1947603510373918
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