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The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc

INTRODUCTION: In the present study, we sought to quantify and contrast the secretome and biomechanical properties of the non-chondrodystrophic (NCD) and chondrodystrophic (CD) canine intervertebral disc (IVD) nucleus pulposus (NP). METHODS: We used iTRAQ proteomic methods to quantify the secretome o...

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Autores principales: Erwin, William Mark, DeSouza, Leroi, Funabashi, Martha, Kawchuk, Greg, Karim, Muhammad Zia, Kim, Sarah, Mӓdler, Stefanie, Matta, Ajay, Wang, Xiaomei, Mehrkens, K. Arne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560915/
https://www.ncbi.nlm.nih.gov/pubmed/26341258
http://dx.doi.org/10.1186/s13075-015-0733-z
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author Erwin, William Mark
DeSouza, Leroi
Funabashi, Martha
Kawchuk, Greg
Karim, Muhammad Zia
Kim, Sarah
Mӓdler, Stefanie
Matta, Ajay
Wang, Xiaomei
Mehrkens, K. Arne
author_facet Erwin, William Mark
DeSouza, Leroi
Funabashi, Martha
Kawchuk, Greg
Karim, Muhammad Zia
Kim, Sarah
Mӓdler, Stefanie
Matta, Ajay
Wang, Xiaomei
Mehrkens, K. Arne
author_sort Erwin, William Mark
collection PubMed
description INTRODUCTION: In the present study, we sought to quantify and contrast the secretome and biomechanical properties of the non-chondrodystrophic (NCD) and chondrodystrophic (CD) canine intervertebral disc (IVD) nucleus pulposus (NP). METHODS: We used iTRAQ proteomic methods to quantify the secretome of both CD and NCD NP. Differential levels of proteins detected were further verified using immunohistochemistry, Western blotting, and proteoglycan extraction in order to evaluate the integrity of the small leucine-rich proteoglycans (SLRPs) decorin and biglycan. Additionally, we used robotic biomechanical testing to evaluate the biomechanical properties of spinal motion segments from both CD and NCD canines. RESULTS: We detected differential levels of decorin, biglycan, and fibronectin, as well as of other important extracellular matrix (ECM)-related proteins, such as fibromodulin and HAPLN1 in the IVD NP obtained from CD canines compared with NCD canines. The core proteins of the vital SLRPs decorin and biglycan were fragmented in CD NP but were intact in the NP of the NCD animals. CD and NCD vertebral motion segments demonstrated significant differences, with the CD segments having less stiffness and a more varied range of motion. CONCLUSIONS: The CD NP recapitulates key elements of human degenerative disc disease. Our data suggest that at least some of the compromised biomechanical properties of the degenerative disc arise from fibrocartilaginous metaplasia of the NP secondary to fragmentation of SLRP core proteins and associated degenerative changes affecting the ECM. This study demonstrates that the degenerative changes that naturally occur within the CD NP make this animal a valuable animal model with which to study IVD degeneration and potential biological therapeutics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0733-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-45609152015-09-06 The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc Erwin, William Mark DeSouza, Leroi Funabashi, Martha Kawchuk, Greg Karim, Muhammad Zia Kim, Sarah Mӓdler, Stefanie Matta, Ajay Wang, Xiaomei Mehrkens, K. Arne Arthritis Res Ther Research Article INTRODUCTION: In the present study, we sought to quantify and contrast the secretome and biomechanical properties of the non-chondrodystrophic (NCD) and chondrodystrophic (CD) canine intervertebral disc (IVD) nucleus pulposus (NP). METHODS: We used iTRAQ proteomic methods to quantify the secretome of both CD and NCD NP. Differential levels of proteins detected were further verified using immunohistochemistry, Western blotting, and proteoglycan extraction in order to evaluate the integrity of the small leucine-rich proteoglycans (SLRPs) decorin and biglycan. Additionally, we used robotic biomechanical testing to evaluate the biomechanical properties of spinal motion segments from both CD and NCD canines. RESULTS: We detected differential levels of decorin, biglycan, and fibronectin, as well as of other important extracellular matrix (ECM)-related proteins, such as fibromodulin and HAPLN1 in the IVD NP obtained from CD canines compared with NCD canines. The core proteins of the vital SLRPs decorin and biglycan were fragmented in CD NP but were intact in the NP of the NCD animals. CD and NCD vertebral motion segments demonstrated significant differences, with the CD segments having less stiffness and a more varied range of motion. CONCLUSIONS: The CD NP recapitulates key elements of human degenerative disc disease. Our data suggest that at least some of the compromised biomechanical properties of the degenerative disc arise from fibrocartilaginous metaplasia of the NP secondary to fragmentation of SLRP core proteins and associated degenerative changes affecting the ECM. This study demonstrates that the degenerative changes that naturally occur within the CD NP make this animal a valuable animal model with which to study IVD degeneration and potential biological therapeutics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0733-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-05 2015 /pmc/articles/PMC4560915/ /pubmed/26341258 http://dx.doi.org/10.1186/s13075-015-0733-z Text en © Erwin et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Erwin, William Mark
DeSouza, Leroi
Funabashi, Martha
Kawchuk, Greg
Karim, Muhammad Zia
Kim, Sarah
Mӓdler, Stefanie
Matta, Ajay
Wang, Xiaomei
Mehrkens, K. Arne
The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
title The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
title_full The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
title_fullStr The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
title_full_unstemmed The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
title_short The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
title_sort biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560915/
https://www.ncbi.nlm.nih.gov/pubmed/26341258
http://dx.doi.org/10.1186/s13075-015-0733-z
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