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Research in veterinary science2004; 77(3); 249-256; doi: 10.1016/j.rvsc.2004.04.005

Effect of matrix depleting agents on the expression of chondrocyte metabolism by equine chondrocytes.

Abstract: This study was carried out to investigate the effect of two enzymes (collagenase and chondroitinase) and two cytokines/metabolites (interleukin-1beta and retinoic acid) of known catabolic activity on the expression of cartilage metabolism/phenotype in equine articular cartilage. Articular cartilage explants from 11 horses (5-13 years old) were treated for 48 h and assayed for total sulphated glycosaminoglycan (GAG), the incorporation of 35S-sulphate, collagen degradation and mRNA expression of the proteoglycans collagen II, collagen IIA, collagen III, collagen IX, collagen X, collagen XI and glyceraldehyde-3-phosphate (GAPDH). Purified collagenase and retinoic acid were responsible for increased GAG loss from the tissues. Chondroitinase, responsible for catalysing the elimination of glucuronate residues from chondroitin A, B and C (Chondroitinase ABC) and retinoic acid treatment induced an inhibition of proteoglycan synthesis, whereas collagenase treatment did not. Collagenase activity was correlated with increased appearance of the CB11B epitope and type II collagen denaturation. By RT-PCR there was evidence of expression of altered collagen type IIA in purified collagenase treated tissues.
Publication Date: 2004-07-28 PubMed ID: 15276777DOI: 10.1016/j.rvsc.2004.04.005Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The study investigates the impact of certain enzymes and substances known to degrade or decompose cartilage on the metabolism of equine cartilage cells. The substances of interest include collagenase and chondroitinase enzymes, as well as the agents interleukin-1beta and retinoic acid.

Research Methodology

  • Articular cartilage samples were obtained from 11 horses between ages 5 and 13. Cartilage samples were treated for 48 hours and then tested.
  • The tests tracked elements such as the overall glycosaminoglycan (GAG) content, incorporation of 35S-sulphate, collagen degradation, and mRNA expression of various proteoglycans.
  • Proteoglycans tested included collagen types II, IIA, III, IX, X, XI as well as glyceraldehyde-3-phosphate (GAPDH).

Findings of the Study

  • The application of purified collagenase and retinoic acid resulted in an increase in GAG loss from the tissues.
  • Treatments with Chondroitinase ABC (which eliminates glucuronate residues from chondroitin types A, B, and C) and retinoic acid brought about a decrease in the synthesis of proteoglycans. However, treatment with collagenase did not have this effect.
  • The observed increase in collagenase activity was associated with a rise in the exposure of the CB11B epitope – an increase in the denaturation of type II collagen.
  • RT-PCR (reverse transcriptase polymerase chain reaction) results indicated signs of the expression of altered collagen type IIA in tissues exposed to purified collagenase.

Interpretation of Results

  • The results suggest specific effects of these catabolic (degrading) substances on the metabolic responses of equine cartilage cells.
  • The increased loss of glycosaminoglycans following treatment with collagenase and retinoic acid suggests these substances may harm the structural integrity of cartilage by reducing its key components.
  • The inhibition of proteoglycan synthesis through the action of chondroitinase and retinoic acid indicates a potential for these agents to slow down or interfere with the natural repair and replenishment processes of cartilage.
  • The identified link between collagenase and the appearance of altered collagen suggest a potential damage and alteration of the cartilage’s key structural protein.

Conclusion

  • The data provides valuable insights into how specific enzymes and substances may trigger or influence degenerative processes in equine cartilage, potentially contributing to conditions such as osteoarthritis or other joint-related pathologies in horses.

Cite This Article

APA
Iqbal J, Bird JL, Hollander AP, Bayliss MT. (2004). Effect of matrix depleting agents on the expression of chondrocyte metabolism by equine chondrocytes. Res Vet Sci, 77(3), 249-256. https://doi.org/10.1016/j.rvsc.2004.04.005

Publication

ISSN: 0034-5288
NlmUniqueID: 0401300
Country: England
Language: English
Volume: 77
Issue: 3
Pages: 249-256

Researcher Affiliations

Iqbal, J
  • Veterinary Basic Sciences Department, Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Hertfordshire AL9 7TA, UK.
Bird, J L
    Hollander, A P
      Bayliss, M T

        MeSH Terms

        • Animals
        • Cartilage, Articular / cytology
        • Chondrocytes / drug effects
        • Chondrocytes / metabolism
        • Chondroitin ABC Lyase / pharmacology
        • Collagen / genetics
        • Collagen / metabolism
        • Collagenases / pharmacology
        • Glyceraldehyde 3-Phosphate / genetics
        • Glyceraldehyde 3-Phosphate / metabolism
        • Glycosaminoglycans / metabolism
        • Horses
        • Interleukin-1 / pharmacology
        • RNA, Messenger / metabolism
        • Reverse Transcriptase Polymerase Chain Reaction / methods
        • Reverse Transcriptase Polymerase Chain Reaction / veterinary
        • Tretinoin / pharmacology

        Citations

        This article has been cited 9 times.
        1. Wu MJM, Sermer C, Kandel RA, Theodoropoulos JS. Characterization of Migratory Cells From Bioengineered Bovine Cartilage in a 3D Co-culture Model. Am J Sports Med 2022 Sep;50(11):3090-3101.
          doi: 10.1177/03635465221113325pubmed: 35983988google scholar: lookup
        2. Alluri VK, Kundimi S, Sengupta K, Golakoti T, Kilari EK. An Anti-Inflammatory Composition of Boswellia serrata Resin Extracts Alleviates Pain and Protects Cartilage in Monoiodoacetate-Induced Osteoarthritis in Rats. Evid Based Complement Alternat Med 2020;2020:7381625.
          doi: 10.1155/2020/7381625pubmed: 32565872google scholar: lookup
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          doi: 10.1089/ten.TEA.2019.0013pubmed: 31237484google scholar: lookup
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          doi: 10.1186/s12917-015-0448-zpubmed: 26116380google scholar: lookup
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        7. Christoffersen M, Woodward E, Bojesen AM, Jacobsen S, Petersen MR, Troedsson MH, Lehn-Jensen H. Inflammatory responses to induced infectious endometritis in mares resistant or susceptible to persistent endometritis. BMC Vet Res 2012 Mar 29;8:41.
          doi: 10.1186/1746-6148-8-41pubmed: 22458733google scholar: lookup
        8. Natoli RM, Revell CM, Athanasiou KA. Chondroitinase ABC treatment results in greater tensile properties of self-assembled tissue-engineered articular cartilage. Tissue Eng Part A 2009 Oct;15(10):3119-28.
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        9. Rockel JS, Kudirka JC, Guzi AJ, Bernier SM. Regulation of Sox9 activity by crosstalk with nuclear factor-kappaB and retinoic acid receptors. Arthritis Res Ther 2008;10(1):R3.
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