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Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit

INTRODUCTION: The porpuse of this animal study was to assess chondrocyte apoptosis and MMP-1, MMP-3 and TIMP-2 expression in rabbit tibial cartilage 6 months after viable medial meniscal autografts and allografts. MATERIAL AND METHODS: Twenty white male New Zealand rabbits were chosen for the study....

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Autores principales: Zwierzchowski, Tomasz J., Stasikowska-Kanicka, Olga, Danilewicz, Marian, Fabiś, Jarosław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542481/
https://www.ncbi.nlm.nih.gov/pubmed/23319989
http://dx.doi.org/10.5114/aoms.2012.30947
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author Zwierzchowski, Tomasz J.
Stasikowska-Kanicka, Olga
Danilewicz, Marian
Fabiś, Jarosław
author_facet Zwierzchowski, Tomasz J.
Stasikowska-Kanicka, Olga
Danilewicz, Marian
Fabiś, Jarosław
author_sort Zwierzchowski, Tomasz J.
collection PubMed
description INTRODUCTION: The porpuse of this animal study was to assess chondrocyte apoptosis and MMP-1, MMP-3 and TIMP-2 expression in rabbit tibial cartilage 6 months after viable medial meniscal autografts and allografts. MATERIAL AND METHODS: Twenty white male New Zealand rabbits were chosen for the study. The medial meniscus was excised from 14 animals and stored under tissue culture conditions for 2 weeks, following which t of them were implantated as autografts and 7 as allografts. The control group consisted of 6 animals which underwent arthtrotomy. When the animals were eutanized, the tibial cartilage was used for immunohisochemical examination. Apoptosis (TUNEL method) and MMP-1, MMP-3 and TIMP-2 expression were estimated semiquantatively. RESULTS: An increased level of chodrocyte apoptosis in the tibail cartilage was observed after both kinds of transplants (p < 0.05), allografts (1.43 ±0.98) and autografts (0.86 ±0.69); no statistical diferences existed between them. An increased level of metalloproteinases and TIMP-2 expression was obreved only after allografts with statistical differences among the allograft group, the autograft group nad the control group (p < 0.05). CONCLUSIONS: Our findings suggest that the meniscal graft does not protect the hyaline cartilage against excessive apoptosis. The results of experimantal studies on humans indicate the need to device a method of apoptosis inhibition in the hyaline cartilage to improve long-term results of meniscal transplantation.
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spelling pubmed-35424812013-01-14 Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit Zwierzchowski, Tomasz J. Stasikowska-Kanicka, Olga Danilewicz, Marian Fabiś, Jarosław Arch Med Sci Experimental Research INTRODUCTION: The porpuse of this animal study was to assess chondrocyte apoptosis and MMP-1, MMP-3 and TIMP-2 expression in rabbit tibial cartilage 6 months after viable medial meniscal autografts and allografts. MATERIAL AND METHODS: Twenty white male New Zealand rabbits were chosen for the study. The medial meniscus was excised from 14 animals and stored under tissue culture conditions for 2 weeks, following which t of them were implantated as autografts and 7 as allografts. The control group consisted of 6 animals which underwent arthtrotomy. When the animals were eutanized, the tibial cartilage was used for immunohisochemical examination. Apoptosis (TUNEL method) and MMP-1, MMP-3 and TIMP-2 expression were estimated semiquantatively. RESULTS: An increased level of chodrocyte apoptosis in the tibail cartilage was observed after both kinds of transplants (p < 0.05), allografts (1.43 ±0.98) and autografts (0.86 ±0.69); no statistical diferences existed between them. An increased level of metalloproteinases and TIMP-2 expression was obreved only after allografts with statistical differences among the allograft group, the autograft group nad the control group (p < 0.05). CONCLUSIONS: Our findings suggest that the meniscal graft does not protect the hyaline cartilage against excessive apoptosis. The results of experimantal studies on humans indicate the need to device a method of apoptosis inhibition in the hyaline cartilage to improve long-term results of meniscal transplantation. Termedia Publishing House 2012-10-08 2012-12-20 /pmc/articles/PMC3542481/ /pubmed/23319989 http://dx.doi.org/10.5114/aoms.2012.30947 Text en Copyright © 2012 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Experimental Research
Zwierzchowski, Tomasz J.
Stasikowska-Kanicka, Olga
Danilewicz, Marian
Fabiś, Jarosław
Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
title Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
title_full Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
title_fullStr Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
title_full_unstemmed Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
title_short Assessment of apoptosis and MMP-1, MMP-3 and TIMP-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
title_sort assessment of apoptosis and mmp-1, mmp-3 and timp-2 expression in tibial hyaline cartilage after viable medial meniscus transplantation in the rabbit
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542481/
https://www.ncbi.nlm.nih.gov/pubmed/23319989
http://dx.doi.org/10.5114/aoms.2012.30947
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