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Arthritis induced immunologically with cationic amidated bovine serum albumin in the Guinea pig

A morphological and biochemical study on the destruction of articular cartilage

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Virchows Archiv B

Summary

Arthritis was induced by injecting cationic amidated bovine serum albumin (aBSA) (pI ∼ 9.2) into the knee joint of immunized guinea pigs and the mechanisms of articular cartilage destruction were studied morphologically and biochemically. Marked synovitis associated with polymorphonuclear leukocyte (PML) infiltration occurred within 1 day of the challenge. Articular cartilage infiltrated by PMLs was almost completely destroyed after 2 weeks. During the initial destructive process, proteoglycans were depleted from the cartilage and later collagen fibers disappeared. Granulation tissue growing in the inflamed synovium and bone marrow replaced the destroyed cartilage and joint cavity and formed fibrous scar tissue (fibrous ankylosis) by 8 weeks. Subsequently, the knee joints developed cartilagenous ankylosis by 12 weeks and finally bony ankylosis at 28 weeks. Autoradiography using125I-aBSA and immunofluorescence studies for immunoglobulin (IgG) and complement (C3) demonstrated that the antigen is trapped in all zones of the articular cartilage and serves as a trigger for immune complex formation. Significantly increased neutral proteinase activities against substrates of proteoglycan subunits, [3H]carboxymethylated transferrin and L-pyroglutamyl-L-prolyl-L-valine-paranitroanilide were detected in homogenates of the synovium and cartilage from arthritic knee joints 1 and 2 weeks after induction. Inhibitor studies and pH curves suggested that the proteinase is leukocyte elastase. Measurable amounts of gelatinolytic activity, detected by activation with 4-aminophenylmercuric acetate and inhibited with EDTA, were also present in the same samples, but there was no detectable collagenase activity. The data on SDS-gelatin substrate gel showed that the proteinase is gelatinase derived from PMLs. These results suggest that in aBSA-induced arthritis, elastase and gelatinase from PMLs invading articular cartilage may play important roles in cartilage destruction.

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References

  • Barrett AJ (1978) The possible role of neutrophil proteinases in damage to articular cartilage. Agents Actions 8:11–18

    Article  PubMed  CAS  Google Scholar 

  • Bieth JG (1986) Elastases: catalytic and biological properties. In: Mecham RP (ed) Biology of Extracellular Matrix: A Series Regulation of Matrix Accumulation. Academic Press Inc, Orland, pp 217–320

    Google Scholar 

  • Burleigh MC, Barrett AJ, Lazarus GS (1974) Cathepsin B1. A lysosomal enzyme that degrades native collagen. Biochem J 137:387–398

    PubMed  CAS  Google Scholar 

  • Chenoweth DE, Hugh TE (1978) Demonstration of specific C5a receptor on intact human polymorphonuclear leukocytes. Proc Natl Acad Sci USA 75:3943–3947

    Article  PubMed  CAS  Google Scholar 

  • Chin JR, Murphy G, Werb Z (1985) Stromelysin, a connective tissue-degrading metalloendopeptidase secreated by stimulated rabbit synovial fibroblasts in parallel with collagenase. J Biol Chem 260:12367–12376

    PubMed  CAS  Google Scholar 

  • Consden R, Doble A, Glynn LE, Nind AP (1971) Production of a chronic arthritis with ovalbumin. Its retention in the rabbit knee joint. Ann Rheum Dis 30:307–315

    PubMed  CAS  Google Scholar 

  • Cooke TD, Jasin HE (1972) The pathogenesis of chronic inflammation in experimental antigen induced arthritis. I. The role of antigen on the local immune response. Arthritis Rheum 15:327–337

    Article  PubMed  CAS  Google Scholar 

  • Danon D, Goldstein L, Marikovsky Y, Skutelsky E (1972) Use of cationized ferritin as a label of negative charges on cell surface. J Ultrastruct Res 38:500–510

    Article  PubMed  CAS  Google Scholar 

  • Fraker PJ, Speck JC Jr (1978) Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycoluril. Biochem Biophys Res Commun 80:849–857

    Article  PubMed  CAS  Google Scholar 

  • Gadher SJ, Eyre DR, Duance VC, Watton SF, Heck LW, Schmid TM, Woolley DE (1988) Susceptibility of cartilage collagens type II, IX, X and XI to human synovial collagenase and neutrophil elastase. Eur J Biochem 175:1–7

    Article  PubMed  CAS  Google Scholar 

  • Ghadially FN, Fuller JA, Kirkaldy-Willis WH (1971) Ultrastructure of full-thickness defects in articular cartilage. Arch Pathol 92:356–369

    PubMed  CAS  Google Scholar 

  • Gisslow MT, McBride BC (1975) A rapid sensitive collagenase assay. Anal Biochem 68:70–78

    Article  PubMed  CAS  Google Scholar 

  • Harris ED Jr, Krane SM (1974) Collagenases. New Engl J Med 291:557–661

    PubMed  CAS  Google Scholar 

  • Hibbs MS, Hasty KA, Seyer JM, Kang AK, Mainardi CL (1985) Biochemical and immunological characterization of the secreted forms of human neutrophil gelatinase. J Biol Chem 260:2493–2500

    PubMed  CAS  Google Scholar 

  • Ishikawa H, Smiley JDS, Ziff M (1975) Electron microscopic demonstration of immunoglobulin deposition in rheumatoid cartilage. Arthritis Rheum 18:563–576

    Article  PubMed  CAS  Google Scholar 

  • Janis R, Hamerman D (1969) Articular cartilage changes in early arthritis. Bull Hosp Joint Dis 30:136–152

    PubMed  CAS  Google Scholar 

  • Janoff A, Feinstem G, Malemud CJ, Elias JM (1976) Degradation of cartilage proteoglycan by human leukocyte granule neutral proteases A model of joint injury. I. Penetration of enzyme into rabbit articular cartilage and release of35SO4-labeled material from the tissue. J Clin Invest 57:615–624

    Article  PubMed  CAS  Google Scholar 

  • Keiser H, Greenwald RA, Feinstein G, Janoff A (1976) Degradation of cartilage proteoglycan by human leukocyte granule neutral proteases A model of joint injury. II. Degradation of isolated bovine nasal cartilage proteoglycan. J Clin Invest 57:625–632

    Article  PubMed  CAS  Google Scholar 

  • Kruijsen MWM, van den Berg WB, van de Putte LBA (1983) Sequential alterations of periarticular structures in antigen-induced arthritis in mice. Histological observations on fibrous capsule, ligaments, bone and muscles, using whole joint sections. Br J Exp Pathol 64:298–305

    PubMed  CAS  Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    PubMed  CAS  Google Scholar 

  • Moriizumi T, Yamashita N, Okada Y (1986) Papain-induced changes in the guinea pig knee joint with special reference to cartilage healing. Virchows Arch B Cell Pathol 51:461–474

    Article  CAS  Google Scholar 

  • Morrison RIG, Barrett AJ, Dingle JT, Prior D (1973) Cathepsin B1 and D. Action on human cartilage proteoglycans. Biochem Biophys Acta 302:411–419

    PubMed  CAS  Google Scholar 

  • Nagase H, Woessner JF Jr (1980) An improved assay for proteases and polysaccharidases employing a cartilage proteoglycan substrate entrapped in polyacrylamide particles. Anal Biochem 107:385–392

    Article  PubMed  CAS  Google Scholar 

  • Okada Y, Nagase H, Harris ED Jr (1986) A metalloproteinase from human rheumatoid synovial fibroblasts that digests connective tissue matrix components. J Biol Chem 261:14245–14255

    PubMed  CAS  Google Scholar 

  • Okada Y, Watanabe S, Nakanishi I, Kishi J, Hayakawa T, Watorek W, Travis J, Nagase H (1988) Inactivation of tissue inhibitor of metalloproteinases by neutrophil elastase and other serine proteinases. FEBS Lett 229:157–160

    Article  PubMed  CAS  Google Scholar 

  • Okada Y, Nakanishi I (1989) Activation of matrix metalloproteinase 3 (stromelysin) and matrix metalloproteinase 2 (gelatinase) by human neutrophil elastase and cathepsin G. FEBS Lett 249:353–356

    Article  PubMed  CAS  Google Scholar 

  • Sandy JD, Sriratana A, Brown HLG, Lowther DA (1981) Evidence for polymorphonuclear-leukocyte derived proteinases in arthritic cartilage. Biochem J 193:193–202

    PubMed  CAS  Google Scholar 

  • Schalkwijk J, van den Berg WB, van de Putte LBA, Joosten LAB (1987) Elastase secreted by activated polymorphonuclear leukocytes causes chondrocyte damage and matrix degradation in intact articular cartilage: escape from inactivation by alpha-Iproteinase inhibitor. Br J Exp Pathol 68:81–88

    PubMed  CAS  Google Scholar 

  • Schalkwijk J, Joosten LAB, van den Berg WB, van de Putte LBA (1988) Degradation of cartilage proteoglycans by elastase is dependent on charge-mediated interactions. Rheumatol Int 8:27–33

    Article  PubMed  CAS  Google Scholar 

  • Ugai K, Ishikawa H, Hirohata K, Shirane H (1983) Interaction of polymorphonuclear leukocytes with immune complexes trapped in rheumatoid articular cartilage. Arthritis Rheum 26:1434–1441

    Article  PubMed  CAS  Google Scholar 

  • Urist MR, Mikulski A, Lietze A (1979) Solubilized and insolubilized bone morphogenetic protein. Proc Natl Acad Sci USA 76:1828–1832

    Article  PubMed  CAS  Google Scholar 

  • Van den Berg WB, van Beusekom HJ, van de Putte LBA, Zwarts WA, van der Sluis M (1982) Antigen handling in antigen-induced arthritis in mice. An autoradiographic and immunofluorescence study using whole joint sections. Am J Pathol 108:9–16

    PubMed  Google Scholar 

  • Van den Berg WB, van de Putte LBA, Zwarts WA, Joosten LAB (1984) Electrical charge of the antigen determines intraarticular antigen handling and chronicity of arthritis in mice. J Clin Invest 74:1850–1859

    Article  PubMed  Google Scholar 

  • Van den Berg WB, van de Putte LBA (1985) Electrical charge of the antigen determines its localization in the mouse knee joint. Deep penetration of cationic BSA in hyaline articular cartilage. Am J Pathol 121:224–234

    PubMed  Google Scholar 

  • Van Lent PLEM, van den Berg WB, Schalkwijk J, van de Putte LBA, van den Bersselaar L (1987) Allergic arthritis induced by cationic antigens: Relationship of chronicity with antigen retention and T cell reactivity. Immunology 62:265–272

    PubMed  Google Scholar 

  • Velvart M, Fehr K (1987) Degradation in vivo of articular cartilage in rheumatoid arthritis and juvenile chronic arthritis by cathepsin G and elastase from polymorphonuclear leukocytes. Rheumatol Int 7:195–202

    Article  PubMed  CAS  Google Scholar 

  • Woessner JF Jr (1973) Mammalian collagenases. Clin Orthop 96:310–326

    PubMed  Google Scholar 

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Yamashita, N., Nakanishi, I. & Okada, Y. Arthritis induced immunologically with cationic amidated bovine serum albumin in the Guinea pig. Virchows Archiv B Cell Pathol 60, 57–66 (1991). https://doi.org/10.1007/BF02899528

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  • DOI: https://doi.org/10.1007/BF02899528

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