Equine carpal articular cartilage fibronectin distribution associated with training, joint location and cartilage deterioration.
Abstract: Processes involved in equine carpal osteochondral injury have not been established. In other species, fibronectin appears important in chondrocyte-matrix interactions, and levels are increased in osteoarthritis. This investigation aimed to (a) describe fibronectin immunoreactivity in the middle carpal joint of 2-year-old Thoroughbreds, (b) determine topographical variations, (c) compare strenuously trained (Group 1) or gently exercised horses (Group 2) and (d) describe sites with early osteoarthritis. Group 1 (n = 6) underwent a 19 week high intensity treadmill training programme. Group 2 (n = 6) underwent 40 min walking until euthanasia. Dorsal and palmar sites on radial, intermediate and third carpal articular surfaces were prepared. Immunohistochemistry was performed using a biotin-streptavidin/peroxidase method. Cross-reactivity of rabbit antihuman fibronectin antiserum with equine fibronectin was confirmed using Western blotting. Results showed: (a) fibronectin was present primarily in pericellular and interterritorial matrix locations, (b) dorsal sites had zonal immunoreactivity compared to palmar sites, (c) Group 1 dorsal radial carpal cartilage had increased superficial staining compared to Group 2 and (d) fibrillated cartilage showed increased intracellular and local matrical immunoreactivity (superficial zone). These findings suggest topographical and exercise-related variations in fibronectin distribution, and indicate equine fibronectin is localised at sites of cartilage degeneration and released into the matrix by chondrocytes in the local area.
Publication Date: 2000-02-08 PubMed ID: 10661385DOI: 10.2746/042516400777611982Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigates how a protein called fibronectin, involved in structural integrity of cartilage, is distributed in the joint cartilage of Thoroughbred horses. The study specifically examined possible links between the distribution of fibronectin and factors like training intensity, joint location, and early-stage osteoarthritis.
Objective and Groups
- The research aimed to study fibronectin usage in joint cartilage of two-year-old Thoroughbreds, determine if there are variations in fibronectin usage across different joint locations, compare fibronectin distributions in heavily trained versus lightly exercised horses, and identify fibronectin distribution in joints showing early signs of osteoarthritis.
- The study was performed on two groups of horses. Group 1 had six horses that underwent high intensity treadmill training for 19 weeks. Group 2 also had six horses, but they were subjected to 40 minutes of walking until euthanasia.
Methodology
- Various joint surfaces were prepared from both the dorsal (back side) and palmar (front side) of the radial, intermediate, and third carpal bones.
- A method called immunohistochemistry was used to observe fibronectin usage within the joint tissues. Cross-reactivity between rabbit antihuman fibronectin antiserum and equine fibronectin was confirmed using a technique called Western blotting.
Results
- Fibronectin was found primarily in pericellular and interterritorial matrix areas of the cartilage, suggesting that it is localised within specific regions rather than being distributed evenly.
- Dorsal joint locations showed regional immunoreactivity when compared to palmar locations, indicating differences in how the protein reacts with the immune system depending on the joint location.
- Horses from Group 1, who underwent strenuous training, displayed increased superficial staining of dorsal radial carpal cartilage compared to Group 2, who were lightly exercised. This implies that more fibronectin is potentially used in heavily exercised horses.
- In samples that exhibited early signs of osteoarthritis (fibrillated cartilage), there was increased intracellular and local matrix immunoreactivity particularly in the superficial zone, pointing to the possibility that fibronectin could be released into the surrounding matrix by local chondrocytes (cartilage cells) at sites of cartilage degeneration.
Implications
- The findings suggest that there are variations in fibronectin distribution depending on the location within the joint and the level of exercise.
- Moreover, the study indicates that fibronectin is localised at sites of cartilage degeneration and may play a role in the development of osteoarthritis in horses.
Cite This Article
APA
Murray RC, Janicke HC, Henson FM, Goodship A.
(2000).
Equine carpal articular cartilage fibronectin distribution associated with training, joint location and cartilage deterioration.
Equine Vet J, 32(1), 47-51.
https://doi.org/10.2746/042516400777611982 Publication
Researcher Affiliations
- Centre for Equine Studies, Animal Health Trust, Kentford, Newmarket, UK.
MeSH Terms
- Animals
- Blotting, Western / veterinary
- Carpus, Animal / chemistry
- Carpus, Animal / immunology
- Carpus, Animal / pathology
- Cartilage, Articular / chemistry
- Cartilage, Articular / immunology
- Cartilage, Articular / physiopathology
- Female
- Fibronectins / analysis
- Fibronectins / immunology
- Horse Diseases / immunology
- Horse Diseases / metabolism
- Horse Diseases / physiopathology
- Horses
- Immunohistochemistry
- Joint Diseases / metabolism
- Joint Diseases / physiopathology
- Joint Diseases / veterinary
- Osteoarthritis / veterinary
- Physical Conditioning, Animal
- Random Allocation
Citations
This article has been cited 3 times.- Anderson JR, Phelan MM, Foddy L, Clegg PD, Peffers MJ. Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study.. J Proteome Res 2020 Sep 4;19(9):3652-3667.
- Henson FM, Vincent T. Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair - effect of BMP-2.. BMC Musculoskelet Disord 2007 Dec 5;8:120.
- Firth EC. The response of bone, articular cartilage and tendon to exercise in the horse.. J Anat 2006 Apr;208(4):513-26.
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