The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc. Issue 1 (December 2015)
- Record Type:
- Journal Article
- Title:
- The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc. Issue 1 (December 2015)
- Main Title:
- The biological basis of degenerative disc disease: proteomic and biomechanical analysis of the canine intervertebral disc
- Authors:
- Erwin, William
DeSouza, Leroi
Funabashi, Martha
Kawchuk, Greg
Karim, Muhammad
Kim, Sarah
Mӓdler, Stefanie
Matta, Ajay
Wang, Xiaomei
Mehrkens, K. - Abstract:
- Abstract 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 NPAbstract 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. … (more)
- Is Part Of:
- Arthritis research & therapy. Volume 17:Issue 1(2015)
- Journal:
- Arthritis research & therapy
- Issue:
- Volume 17:Issue 1(2015)
- Issue Display:
- Volume 17, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 17
- Issue:
- 1
- Issue Sort Value:
- 2015-0017-0001-0000
- Page Start:
- 1
- Page End:
- 13
- Publication Date:
- 2015-12
- Subjects:
- Arthritis -- Periodicals
Arthritis -- Treatment -- Periodicals
616.722005 - Journal URLs:
- http://arthritis-research.com ↗
http://pubmedcentral.gov/tocrender.fcgi?journal=135 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s13075-015-0733-z ↗
- Languages:
- English
- ISSNs:
- 1478-6362
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9669.xml