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Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression

BACKGROUND: The present study was conducted to address whether the intervertebral disc of rabbit could be considered (i) as a valuable model to provide new insights into the tissue and cellular changes of Nucleus pulposus aging and (ii) as an appropriate tool to investigate the efficacy of Nucleus p...

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Autores principales: Clouet, Johann, Pot-Vaucel, Marianne, Grimandi, Gaël, Masson, Martial, Lesoeur, Julie, Fellah, Borhane H, Gauthier, Olivier, Fusellier, Marion, Cherel, Yan, Maugars, Yves, Guicheux, Jérôme, Vinatier, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150337/
https://www.ncbi.nlm.nih.gov/pubmed/21726455
http://dx.doi.org/10.1186/1471-2474-12-147
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author Clouet, Johann
Pot-Vaucel, Marianne
Grimandi, Gaël
Masson, Martial
Lesoeur, Julie
Fellah, Borhane H
Gauthier, Olivier
Fusellier, Marion
Cherel, Yan
Maugars, Yves
Guicheux, Jérôme
Vinatier, Claire
author_facet Clouet, Johann
Pot-Vaucel, Marianne
Grimandi, Gaël
Masson, Martial
Lesoeur, Julie
Fellah, Borhane H
Gauthier, Olivier
Fusellier, Marion
Cherel, Yan
Maugars, Yves
Guicheux, Jérôme
Vinatier, Claire
author_sort Clouet, Johann
collection PubMed
description BACKGROUND: The present study was conducted to address whether the intervertebral disc of rabbit could be considered (i) as a valuable model to provide new insights into the tissue and cellular changes of Nucleus pulposus aging and (ii) as an appropriate tool to investigate the efficacy of Nucleus pulposus cell-based biotherapies. METHODS: Lumbar intervertebral disc from rabbits with increasing ages (1, 6 and 30 month-old) were compared by MRI and histological observation using Pfirrmann's grading and Boos' scoring respectively. The expression of transcripts (COL2A1, AGC1, COL1A1, MMP13, BMP2, MGP and p21) in Nucleus pulposus cells were analysed by quantitative real-time PCR. RESULTS: MRI analysis indicated an early age-dependent increase in the Pfirrmann's grading. Histological Boos' scoring was also increased. The analysis of transcript expression levels showed that COL2A1 and AGC1 were down-regulated as a function of age. Conversely, COL1A1, MMP-13, BMP-2, MGP and p21 were significantly up-regulated in the Nucleus pulposus cells of aged rabbit intervertebral disc. CONCLUSIONS: Our study describes the consistency of the rabbit as a model of intervertebral disc changes as a function of age by correlating tissue alteration with cellular modification measured.
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spelling pubmed-31503372011-08-05 Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression Clouet, Johann Pot-Vaucel, Marianne Grimandi, Gaël Masson, Martial Lesoeur, Julie Fellah, Borhane H Gauthier, Olivier Fusellier, Marion Cherel, Yan Maugars, Yves Guicheux, Jérôme Vinatier, Claire BMC Musculoskelet Disord Research Article BACKGROUND: The present study was conducted to address whether the intervertebral disc of rabbit could be considered (i) as a valuable model to provide new insights into the tissue and cellular changes of Nucleus pulposus aging and (ii) as an appropriate tool to investigate the efficacy of Nucleus pulposus cell-based biotherapies. METHODS: Lumbar intervertebral disc from rabbits with increasing ages (1, 6 and 30 month-old) were compared by MRI and histological observation using Pfirrmann's grading and Boos' scoring respectively. The expression of transcripts (COL2A1, AGC1, COL1A1, MMP13, BMP2, MGP and p21) in Nucleus pulposus cells were analysed by quantitative real-time PCR. RESULTS: MRI analysis indicated an early age-dependent increase in the Pfirrmann's grading. Histological Boos' scoring was also increased. The analysis of transcript expression levels showed that COL2A1 and AGC1 were down-regulated as a function of age. Conversely, COL1A1, MMP-13, BMP-2, MGP and p21 were significantly up-regulated in the Nucleus pulposus cells of aged rabbit intervertebral disc. CONCLUSIONS: Our study describes the consistency of the rabbit as a model of intervertebral disc changes as a function of age by correlating tissue alteration with cellular modification measured. BioMed Central 2011-07-04 /pmc/articles/PMC3150337/ /pubmed/21726455 http://dx.doi.org/10.1186/1471-2474-12-147 Text en Copyright ©2011 Clouet et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Clouet, Johann
Pot-Vaucel, Marianne
Grimandi, Gaël
Masson, Martial
Lesoeur, Julie
Fellah, Borhane H
Gauthier, Olivier
Fusellier, Marion
Cherel, Yan
Maugars, Yves
Guicheux, Jérôme
Vinatier, Claire
Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression
title Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression
title_full Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression
title_fullStr Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression
title_full_unstemmed Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression
title_short Characterization of the age-dependent intervertebral disc changes in rabbit by correlation between MRI, histology and gene expression
title_sort characterization of the age-dependent intervertebral disc changes in rabbit by correlation between mri, histology and gene expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150337/
https://www.ncbi.nlm.nih.gov/pubmed/21726455
http://dx.doi.org/10.1186/1471-2474-12-147
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