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Effect of interleukin 1 on articular cartilage from young and aged horses and comparison with metabolism of osteoarthritic cartilage.

Abstract: The effect of interleukin 1 (IL-1) on equine articular cartilage was investigated, using a cartilage explant culture system. Measurement of [35S]O4 incorporation revealed synthesis of matrix proteoglycan by cartilage to be decreased 45, 59.7, and 37.5% after 1, 3, and 5 days, respectively, in culture in the presence of 5 U of IL-1/ml. There was no change in proteoglycan degradation as determined by measurement of [35S]O4 release into the culture medium. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of cartilage-conditioned medium indicated that exposure of cartilage to IL-1 caused a decrease in total protein synthesis by 45, 68, and 87% after 1, 3, and 5 days, respectively, in culture while selectively inducing synthesis of the 57-kd neutral metalloproteinase stromelysin (matrix metalloproteinase-3) in young and adult horses. Identification of stromelysin was confirmed by functional characterization and immunoprecipitation. Baseline total protein synthesis, as well as specific synthesis of stromelysin in cartilage from adult and aged horses, was markedly less than that of young horses. The IL-1-induced reduction in total protein synthesis may not be a characteristic of equine articular cartilage from affected joints of horses with naturally acquired osteoarthritis as indicated by an overall increase in protein synthesis by osteoarthritic explants. Introduction of IL-1 into an equine articular cartilage explant culture system resulted in decrease of matrix component synthesis and increase in specific degradative enzyme synthesis and activity. Articular cartilage from aged horses had markedly less overall metabolic activity, compared with cartilage from young horses.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1994-01-01 PubMed ID: 8141486
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research investigates how interleukin 1 (IL-1), a molecule component of the immune system, affects the cartilage of young and aged horses, also comparing it to the metabolism of osteoarthritic cartilage. It was found that IL-1 decreases the synthesis of matrix components in articular cartilage, while simultaneously increasing the production and activity of a particular degradating enzyme. Aged horses exhibited less overall metabolic activity in their cartilage compared to young horses.

Research Methodology

  • The researchers investigated the effect of interleukin 1 (IL-1), an cytokine component of the immune system, on equine articular cartilage using a culture system created from cartilage tissue (cartilage explant).
  • The process of matrix proteoglycan synthesis was measured using [35S]O4 incorporation into the cartilage.
  • They investigated the degradation of proteoglycan by measuring [35S]O4 release from the cartilage into the medium of the culture system.
  • The team studied the synthesis of total protein by the cartilage and the synthesis of a specific enzyme called stromelysin (a metalloproteinase-3) through Sodium dodecyl sulfate-polyacrylamide gel electrophoresis method.

Research Findings

  • The study revealed that the presence of IL-1 in the culture system decreased the matrix proteoglycan synthesis by cartilage significantly over time (45, 59.7, and 37.5% after 1, 3, and 5 days respectively).
  • They found no alteration in the process of proteoglycan degradation.
  • The research indicated that cartilage exposed to IL-1 decreased total protein synthesis progressively (45, 68, and 87% after 1, 3, and 5 days respectively) while selectively inducing the synthesis of the metalloproteinase-3 enzyme stromelysin.
  • A comparative study revealed that the baseline total protein synthesis and the synthesis of stromelysin by articular cartilage from adult and aged horses was substantially less than that by young horses.
  • The research also found that IL-1-induced reduction in total protein synthesis might not be a feature of equine articular cartilage from joints affected by osteoarthritis natural to horses. This was based on the observed overall increase in protein synthesis by osteoarthritic tissues in the culture system.

Conclusion

  • The introduction of IL-1 into an equine cartilage culture media resulted in decreased synthesis of matrix components and an increased synthesis and activity of a specific degradation enzyme.
  • Aged horses exhibited less overall metabolic activity in their cartilage compared to young horses, implying that age, too, plays a significant role in cartilage metabolism.

Cite This Article

APA
Morris EA, Treadwell BV. (1994). Effect of interleukin 1 on articular cartilage from young and aged horses and comparison with metabolism of osteoarthritic cartilage. Am J Vet Res, 55(1), 138-146.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 55
Issue: 1
Pages: 138-146

Researcher Affiliations

Morris, E A
  • Department of Medicine, Tufts University School of Veterinary Medicine, North Grafton, MA 01536.
Treadwell, B V

    MeSH Terms

    • Aging / metabolism
    • Animals
    • Animals, Newborn
    • Cartilage, Articular / drug effects
    • Cartilage, Articular / growth & development
    • Cartilage, Articular / metabolism
    • Electrophoresis, Polyacrylamide Gel
    • Horse Diseases
    • Horses / metabolism
    • Humans
    • Interleukin-1 / pharmacology
    • Metalloendopeptidases
    • Methionine / metabolism
    • Organ Culture Techniques
    • Osteoarthritis / metabolism
    • Osteoarthritis / veterinary
    • Peptide Hydrolases / isolation & purification
    • Peptide Hydrolases / metabolism
    • Protein Biosynthesis
    • Proteins / isolation & purification
    • Proteoglycans / biosynthesis
    • Proteoglycans / isolation & purification
    • Proteoglycans / metabolism
    • Recombinant Proteins / pharmacology
    • Sulfates / metabolism
    • Sulfur Radioisotopes

    Citations

    This article has been cited 5 times.
    1. Menarim BC, Gillis KH, Oliver A, Ngo Y, Werre SR, Barrett SH, Rodgerson DH, Dahlgren LA. Macrophage Activation in the Synovium of Healthy and Osteoarthritic Equine Joints. Front Vet Sci 2020;7:568756.
      doi: 10.3389/fvets.2020.568756pubmed: 33324696google scholar: lookup
    2. Li KW, Siraj SA, Cheng EW, Awada M, Hellerstein MK, Turner SM. A stable isotope method for the simultaneous measurement of matrix synthesis and cell proliferation in articular cartilage in vivo. Osteoarthritis Cartilage 2009 Jul;17(7):923-32.
      doi: 10.1016/j.joca.2009.01.006pubmed: 19230856google scholar: lookup
    3. Tung JT, Fenton JI, Arnold C, Alexander L, Yuzbasiyan-Gurkan V, Venta PJ, Peters TL, Orth MW, Richardson DW, Caron JP. Recombinant equine interleukin-1beta induces putative mediators of articular cartilage degradation in equine chondrocytes. Can J Vet Res 2002 Jan;66(1):19-25.
      pubmed: 11858644
    4. Chaimbeul SF, Rodrigues NNP, Thurston DD, Scoggin KE, Janes J, Jacobs CA, MacLeod JN, Stone AV, Menarim BC. PPARγ Agonism Modulates Synovial Macrophage and Cartilage Responses in an Equine Model of Synovial Inflammation-Implications for Joint Therapy. Biomolecules 2025 Sep 1;15(9).
      doi: 10.3390/biom15091267pubmed: 41008574google scholar: lookup
    5. Gabriel N, Innes JF, Caterson B, Vaughan-Thomas A. Development of an in vitro model of feline cartilage degradation. J Feline Med Surg 2010 Aug;12(8):614-20.
      doi: 10.1016/j.jfms.2010.03.007pubmed: 20471881google scholar: lookup