Use of proteomic analysis to determine the protein constituents of synovial fluid samples from the stifle joints of dogs with and without osteoarthritis secondary to cranial cruciate ligament rupture

Muhammad Shahid Small Animal Clinic, Freie Universität Berlin, D-14163 Berlin, Germany.

Search for other papers by Muhammad Shahid in
Current site
Google Scholar
PubMed
Close
 DVM, MPhil
,
George Manchi Small Animal Clinic, Freie Universität Berlin, D-14163 Berlin, Germany.

Search for other papers by George Manchi in
Current site
Google Scholar
PubMed
Close
 DVM, Dr Med Vet
,
Leo Brunnberg Small Animal Clinic, Freie Universität Berlin, D-14163 Berlin, Germany.

Search for other papers by Leo Brunnberg in
Current site
Google Scholar
PubMed
Close
 DVM, Dr Med Vet Habil
, and
Jens Raila Institute of Nutritional Science, University of Potsdam 114-116, D-14558 Potsdam-Rehbrücke, Germany.

Search for other papers by Jens Raila in
Current site
Google Scholar
PubMed
Close
 DVM, Dr Med Vet Habil

Abstract

OBJECTIVE To use proteomic analysis to determine the protein constituents of synovial fluid samples from the stifle joints of dogs with and without osteoarthritis secondary to cranial cruciate ligament rupture (CCLR).

ANIMALS 12 dogs with clinically normal stifle joints (controls) and 16 dogs with osteoarthritis secondary to CCLR.

PROCEDURES A synovial fluid sample was obtained from all dogs. Synovial fluid total protein concentration was determined by the Bradford assay. Proteins were separated by use of a 1-D SDS-PAGE to detect protein bands that differed between dogs with and without osteoarthritis. Those protein bands then underwent trypsin digestion and were analyzed by matrix-assisted laser desorption-ionization time-of-flight mass spectrometry, the results of which were compared with a curated protein sequence database for protein identification. One of the most frequently identified proteins, apoprotein (apo) A-I, was then quantified in all synovial fluid samples by use of a competitive-inhibition ELISA. Results were compared between dogs with and without osteoarthritis.

RESULTS Median synovial fluid total protein and apo A-I concentrations for dogs with osteoarthritis were significantly greater than those for control dogs. The most abundant proteins identified in the synovial fluid were albumin and apo A-I.

CONCLUSIONS AND CLINICAL RELEVANCE Results indicated that quantification of synovial fluid total protein and apo A-I concentrations might facilitate diagnosis of osteoarthritis secondary to CCLR in dogs. Further research and validation of synovial fluid apo A-I concentration as a biomarker for osteoarthritis in dogs are necessary before it can be recommended for clinical use.

Abstract

OBJECTIVE To use proteomic analysis to determine the protein constituents of synovial fluid samples from the stifle joints of dogs with and without osteoarthritis secondary to cranial cruciate ligament rupture (CCLR).

ANIMALS 12 dogs with clinically normal stifle joints (controls) and 16 dogs with osteoarthritis secondary to CCLR.

PROCEDURES A synovial fluid sample was obtained from all dogs. Synovial fluid total protein concentration was determined by the Bradford assay. Proteins were separated by use of a 1-D SDS-PAGE to detect protein bands that differed between dogs with and without osteoarthritis. Those protein bands then underwent trypsin digestion and were analyzed by matrix-assisted laser desorption-ionization time-of-flight mass spectrometry, the results of which were compared with a curated protein sequence database for protein identification. One of the most frequently identified proteins, apoprotein (apo) A-I, was then quantified in all synovial fluid samples by use of a competitive-inhibition ELISA. Results were compared between dogs with and without osteoarthritis.

RESULTS Median synovial fluid total protein and apo A-I concentrations for dogs with osteoarthritis were significantly greater than those for control dogs. The most abundant proteins identified in the synovial fluid were albumin and apo A-I.

CONCLUSIONS AND CLINICAL RELEVANCE Results indicated that quantification of synovial fluid total protein and apo A-I concentrations might facilitate diagnosis of osteoarthritis secondary to CCLR in dogs. Further research and validation of synovial fluid apo A-I concentration as a biomarker for osteoarthritis in dogs are necessary before it can be recommended for clinical use.

Contributor Notes

Address correspondence to Dr. Raila (jens.raila@uni-potsdam.de).
  • 1. Garner BC, Stoker AM, Kuroki K, et al. Using animal models in osteoarthritis biomarker research. J Knee Surg 2011;24:251–264.

  • 2. Wieland HA, Michaelis M, Kirschbaum BJ, et al. Osteoarthritis—an untreatable disease? Nat Rev Drug Discov 2005;4:331–344.

  • 3. Hegemann N, Kohn B, Brunnberg L, et al. Biomarkers of joint tissue metabolism in canine osteoarthritic and arthritic joint disorders. Osteoarthritis Cartilage 2002;10:714–721.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 4. Johnson KA, Hay CW, Chu Q, et al. Cartilage-derived biomarkers of osteoarthritis in synovial fluid of dogs with naturally acquired rupture of the cranial cruciate ligament. Am J Vet Res 2002;63:775–781.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5. Aragon CL, Budsberg SC. Applications of evidence-based medicine: cranial cruciate ligament injury repair in the dog. Vet Surg 2005;34:93–98.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 6. Wilke VL, Robinson DA, Evans RB, et al. Estimate of the annual economic impact of treatment of cranial cruciate ligament injury in dogs in the United States. J Am Vet Med Assoc 2005;227:1604–1607.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7. Goldstein RE. Swollen joints and lameness. In: Ettinger SJ, Feldman EC, eds. Textbook of veterinary internal medicine. 6th ed. St Louis: Elsevier Saunders, 2005;83–87.

    • Search Google Scholar
    • Export Citation
  • 8. Shahid M, Manchi G, Slunsky P, et al. A systemic review of existing serological possibilities to diagnose canine osteoarthritis with a particular focus on extracellular matrix proteoglycans and protein. Pol J Vet Sci 2017;20:189–201.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9. de Bakker E, Stroobants V, VanDael F, et al. Canine synovial fluid biomarkers for early detection and monitoring of osteoarthritis. Vet Rec 2017;180:328–329.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10. Qi C, Changlin H. Levels of biomarkers correlate with magnetic resonance imaging progression of knee cartilage degeneration: a study on canine. Knee Surg Sports Traumatol Arthrosc 2007;15:869–878.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11. Ritter SY, Subbaiah R, Bebek G, et al. Proteomic analysis of synovial fluid from the osteoarthritic knee: comparison with transcriptome analyses of joint tissues. Arthritis Rheum 2013;65:981–992.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12. Chiaradia E, Pepe M, Tartaglia M, et al. Gambling on putative biomarkers of osteoarthritis and osteochondrosis by equine synovial fluid proteomics. J Proteomics 2012;75:4478–4493.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13. Garner BC, Kuroki K, Stoker AM, et al. Expression of proteins in serum, synovial fluid, synovial membrane, and articular cartilage samples obtained from dogs with stifle joint osteoarthritis secondary to cranial cruciate ligament disease and dogs without stifle joint arthritis. Am J Vet Res 2013;74:386–394.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14. Skiöldebrand E, Ekman S, Mattsson Hultén L, et al. Cartilage oligomeric matrix protein neoepitope in the synovial fluid of horses with acute lameness: a new biomarker for the early stages of osteoarthritis. Equine Vet J 2017;49:662–667.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15. Gibson DS, Rooney ME. The human synovial fluid proteome: a key factor in the pathology of joint disease. Proteomics Clin Appl 2007;1:889–899.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16. Smith MA, Bains SK, Betts JC, et al. Use of two-dimensional gel electrophoresis to measure changes in synovial fluid proteins from patients with rheumatoid arthritis treated with antibody to CD4. Clin Diagn Lab Immunol 2001;8:105–111.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 17. Harasen G. Diagnosing rupture of the cranial cruciate ligament. Can Vet J 2002;43:475–476.

  • 18. AVMA. AVMA guidelines for the euthanasia of animals: 2013 edition. Available at: www.avma.org/KB/Policies/Documents/euthanasia.pdf. Accessed Oct 15, 2014.

    • Search Google Scholar
    • Export Citation
  • 19. Candiano G, Bruschi M, Musante L, et al. Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis. Electrophoresis 2004;25:1327–1333.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 20. Schaefer H, Kohn B, Schweigert FJ, et al. Quantitative and qualitative urine protein excretion in dogs with severe inflammatory response syndrome. J Vet Intern Med 2011;25:1292–1297.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 21. Reeg S, Jung T, Castro JP, et al. The molecular chaperone Hsp70 promotes the proteolytic removal of oxidatively damaged proteins by the proteasome. Free Radic Biol Med 2016;99:153–166.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 22. Perkins DN, Pappin DJ, Creasy DM, et al. Probability-based protein identification by searching sequence databases using mass spectrometry data. Electrophoresis 1999;20:3551–3567.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23. Janssen J, Laatz W. Statistische Datenanalyse mit SPSS: Eine anwendungsorientierte Einführung in das Basissystem und das Modul Exakte Tests. Berlin: Springer-Gabler, 2017;601–660.

    • Search Google Scholar
    • Export Citation
  • 24. Str⊘m H, Alexandersen S, Poulsen OM, et al. Synovial fluid proteins in degenerative joint disease in dogs. Vet Immunol Immunopathol 1989;22:187–196.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 25. Walter EL, Spreng D, Schmöckel H, et al. Distribution of lactate dehydrogenase in healthy and degenerative canine stifle joint cartilage. Histochem Cell Biol 2007;128:7–18.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26. Murakami K, Yonezawa T, Matsuki N. Synovial fluid total protein concentration as a possible marker for canine idiopathic polyarthritis. J Vet Med Sci 2016;77:1715–1717.

    • Search Google Scholar
    • Export Citation
  • 27. Gharbi M, Sanchez C, Mazzucchelli G, et al. Identification of differential pattern of protein expression in canine osteoarthritis serum after anterior cruciate ligament transection: a proteomic analysis. Vet J 2013;197:848–853.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 28. Ceron JJ, Eckersall PD, Martýnez-Subiela S. Acute phase proteins in dogs and cats: current knowledge and future perspectives. Vet Clin Pathol 2005;34:85–99.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 29. Cretu D, Diamandis EP, Chandran V. Delineating the synovial fluid proteome: recent advancements and ongoing challenges in biomarker research. Crit Rev Clin Lab Sci 2013;50:51–63.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 30. Gibson DS, Blelock S, Curry J, et al. Comparative analysis of synovial fluid and plasma proteomes in juvenile arthritis-proteomic patterns of joint inflammation in early stage disease. J Proteomics 2009;72:656–676.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 31. Oliviero F, Sfriso P, Baldo G, et al. Apolipoprotein A-I and cholesterol in synovial fluid of patients with rheumatoid arthritis, psoriatic arthritis and osteoarthritis. Clin Exp Rheumatol 2009;27:79–83.

    • Search Google Scholar
    • Export Citation
  • 32. Hyka N, Dayer JM, Modoux C, et al. Apolipoprotein A-I inhibits the production of interleukin-1β and tumor necrosis factor-α by blocking contact-mediated activation of monocytes by T lymphocytes. Blood 2001;97:2381–2389.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 33. Wu BJ, Ong KL, Shrestha S, et al. Inhibition of arthritis in the Lewis rat by apolipoprotein A-I and reconstituted high-density lipoproteins. Arterioscler Thromb Vasc Biol 2014;34:543–551.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 34. Terkeltaub R. Apolipoprotein A-I at the interface of vascular inflammation and arthritis. Arterioscler Thromb Vasc Biol 2014;34:474–476.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 35. de Seny D, Cobraiville G, Charlier E, et al. Apolipoprotein-A1 as a damage-associated molecular patterns protein in osteoarthritis: ex vivo and in vitro proinflammatory properties. PLoS One 2015;10:e0122904.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 36. Ananth L, Prete PE, Kashyap ML. Apolipoproteins A-I and B and cholesterol in synovial fluid of patients with rheumatoid arthritis. Metabolism 1993;42:803–806.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 37. Rosenkranz ME, Wilson DC, Marinov AD, et al. Synovial fluid proteins differentiate between the subtypes of juvenile idiopathic arthritis. Arthritis Rheum 2010;62:1813–1823.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 38. Trocmé C, Marotte H, Baillet A, et al. Apolipoprotein A-I and platelet factor 4 are biomarkers for infliximab response in rheumatoid arthritis. Ann Rheum Dis 2009;68:1328–1333.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 39. Bresnihan B, Gogarty M, FitzGerald O, et al. Apolipoprotein A-I infiltration in rheumatoid arthritis synovial tissue: a control mechanism of cytokine production? Arthritis Res Ther 2004;6:R563–R566.

    • Crossref
    • Search Google Scholar
    • Export Citation

Advertisement