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ORIGINAL ARTICLE

Expression of wnt signaling molecules in the synovial membranes of rabbit ankle joints injected with Enterococcus faecalis cell fractions

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Pages 35-43 | Received 15 Jan 2002, Accepted 09 Jul 2002, Published online: 02 Jan 2014

References

  • Koch AE. Review. Angiogenesis: implications for rheumatoid arthritis. Arthritis Rheum 1998;41:951–62.
  • Goronzy JJ, Zettl A, Weyand CM. T cell receptor repertoire in rheumatoid arthritis. Int Rev Immunol 1998;17:339–63.
  • Ohba T, Takase Y, Ohhara M, Kasukawa R. Thrombin in the synovial fluid of patients with rheumatoid arthritis mediates prolif-eration of synovial fibroblast-like cells by induction of platelet-derived growth factor. J Ftheumatol 1996;23:1505–11.
  • Bresnihan B. Pathogenesis of joint damage in rheumatoid arthritis. J Ftheumatol 1999;26:717–9.
  • Cromartie WJ, Craddock JG, Schwab JH, Anderle SK, Yang CH. Arthritis in rats after systemic injection of streptococcal cells or cell walls. J Exp Med 1977;146:1585–602.
  • Schwab JH, Cromartie WJ, Ohanian SH, Craddock JG. Associa-tion of experimental chronic arthritis with the persistence of groupD streptococcal cell walls in the articular tissue. J Bacteriol 1967;94:1728–35.
  • Lehman TJA, Allen JB, Plotz PH, Willeer RL. Poly-arthritis in rats following the systemic injection of Lactobacillus casei cell walls in aqueous suspension. Arthritis Rheum 1983;26:1259–65.
  • Fox A, Brown RR, Anderle SK, Chetty C, Cromartie WJ, Gooder H, et al. Arthropathic properties related to the molecular weight of peptidoglycan-polysaccharide polymers of streptococcal cell walls. Infect Immun 1982;35:1003–10.
  • Cromartie WJ. Arthropathic properties of peptidoglycan-poly-saccharide complexes of microbial origin. In: Deicher H, Schulz LCI, editors. Arthritis: models and mechanisms. Berlin: Springer; 1981. p. 24–38.
  • Stimpson SA, Brown RR, Anderle SK, Klapper DG, Clark RL, Cromartie WJ, et al. Arthropathic properties of cell wall polymers from normal flora bacteria. Infect Immun 1986;51:240–9.
  • Ohanian SH, Schwab JH. Persistence of group A streptococcal cell walls related to chronic inflammation of rabbit darmal connective tissue. J Exp Med 1967;125:1137–48.
  • Monier S, Reme T, Cognot C, Gao QL, Travaglio-Encinoza A, Cuchacovich M, et al. Growth factor activity of IL-6 in the synovial fluid of patients with rheumatoid arthritis. Chin Exp Ftheumatol 1994;12: 595–602.
  • Badolato R, Oppenheim JJ. Role of cytokines, acute-phase pro-teins, and chemokines in the progression of rheumatoid arthritis. Semin Arthritis Rheum 1996;26:526–38.
  • Peichl P, Pursch E, Broll H, Lindley U. Anti-IL-8 autoantibodies and complexes in rheumatoid arthritis: polyclonal activation in chronic synovial tissue inflammation. Ftheumatol Int 1999;18:141–5.
  • Harada S, Yamamura M, Okamoto H, Morita Y, Kawashima M, Aita T, et al. Production of interleukin-7 and interleukin-15 by fibroblast-like synoviocytes from patients with rheumatoid arthri-tis. Arthritis Rheum 1999;42:1508–16.
  • Klingensmith J, Nusse R. Signaling by wingless in Drosophila. Dev Biol 1994;166:396–414.
  • Cadigan KM, Nusse R. Wnt signaling: a common theme in animal development. Genes Dev 1997;11:3286–305.
  • Miller JR, Moon RT. Signal transduction through p-catenin and specification of cell fate during embryogenesis. Genes Dev 1996;10:2527–39.
  • Molenaar M, van de Wetering M, Oosterwegel M, Petersonmaduro J, Godsave S, Korinek V. Xtcf-3 transcription factor mediates p-catenin-induced axis formation in Xenopus embryos. Cell 1996;86:391–99.
  • Bhanot P, Brink M, Samos CH, Hsieh J-C, Wang Y, Macke JP, et al. A new member of the frizzled family from Drosophila functions as a wingless receptor. Nature 1996;382:225–30.
  • Vinson CR, Conover S, Adler PN. A Drosophila tissue polarity locus encodes a protein containing seven potential transmembrane domains. Nature 1989;338:263–4.
  • Blankesteijn WM, Essers-Janssen YP, Ulrich MM, Smits JF. In-creased expression of a homologue of Drosophila tissue polarity gene "frizzled" in left ventricular hypertrophy in the rat, as identi-fied by subtractive hybridization. J Mol Cell Cardiol 1996;28:1187–91.
  • Takada H, Tsujimoto M, Kotani S, Kusumoto S, Inage M, Shiba T, et al. Mitogenic effects of bacterial cell walls, their fragments and related synthetic compounds on thymocytes and splenocytes of guinea pigs. Infect Immun 1979;25:645–52.
  • Trentham DE, Townes AS, Kaug AH. Autoimmunity to type II collagens: an experimental model of arthritis. J Exp Med 1977;146:857–68.
  • Pearson CM, Waksman BH, Sharp JT. Studies of arhritis and other lesions induced in rats by injection of mycobacterial adjuvant. J Exp Med 1961;113:485–90.
  • Koga T, Kakimoto K, Hirofuji T, Kotani S, Ohkuni H, Watanabe K, et al. Acute joint inflammation in mice after systemic injection of the cell wall, its peptidoglycan, and chemically defined pepti-doglycan subunits from various bacteria. Infect Immun 1985;50:27–34.
  • Ichimura 0, Suzuki S, Saito M, Sugawara Y, Ishida N. Augmenta-tion of interleukin-1 and interleukin-2 production by 0K-432. Int J Immunopharmacol 1985;7: 263–70.
  • Saito M, Ebina T, Koi M, Yamaguchi T, Kawada Y, Ishida N. Induction of interferon-y in mouse spleen cells by 0K-432, a preparation of Streptococcus pyogenes. Cell Immunol 1982;68:187–92.
  • Yamamoto A, Nagamura M, Usai H, Sugawara Y, Watanabe H, Niitsu Y, et al. Release of tumor necrosis factor (TNF) into mouse peritoneal fluids by 0K-432, a streptococcal preparation. Immunopharmacology 1986;11:79–86.
  • Firestein GS, Alvaro-Garcoa JM, Maki R. Quantitative analysis of cytokine gene expression in rheumatoid arthritis. J Immunol 1990;144:3347–53.
  • Fontana A, Hengartner H, Weber E, Fejr K, Grob PJ, Cohen G. Interleukin-1 activity in the synovial fluid of patients with rheuma-toid arthritis. Ftheumatol Int 1982;2:49–53.
  • Chu CQ, Field M, Feldman M, Maini RN. Localization of tumor necrosis factor-a in synovial tissues and at the cartilage-pannus junction in patients with rheumatoid arthritis. Arthritis Rheum 1991;34:1125–32.
  • Feige U, Karbowski A, Rordorf-Adam C, Pataki A. Arthritis in-duced by continuous infusion of hr-interleukin-1-a into the rabbit knee joint. Int J Tissue React 1989;11: 225–38.
  • Fuseler JW, Conner EM, Davis JM, Wolf RE, Grisham MB. Cytokine and nitric oxide production in the acute phase of bacte-rial cell-wall-induced arthritis. Inflammation 1997;21:113–31.
  • Nusse R, Varmus HE. wnt genes. Cell 1992;69:1073–87.
  • Theisen H, Purcell J, Bennet M, Kansagara D, Syed A, Marsh J. Dishevelled is required during wingless signaling to establish both cell polarity and cell identity. Development 1994;120:347–60.
  • Yanagawa S-I, Leeuwen FV, Woderz A, Klingensmith J, Nusse R. The dishevelled protein is modified by wingless signaling in Droso-phila. Genes Dev 1995;9:1087–97.
  • Siegfried E, Wilder EL, Perrimon N. Components of wingless sig-naling in Drosophila. Nature 1994;367:76–80.
  • Peifer M. Regulating cell proliferation: as easy as APC. Science 1996;272:974–5.
  • Kawahara K, Morishita T, Nakamura T, Hamada F, Toyoshima K, Akiyama T. Down regulation of p - cat enin by the colorectal tumor suppressor APC requires association with Axin and p-catenin. J Biol Chem 2000;275:8369–74.
  • Zeng L, Fagotto F, Zhang T, Hsu W, Vasicek TJ, Perry WL, et al. The mouse fused locus encodes Axin, an inhibitor of the wnt signaling pathway that regulates embryonic axis formation. Cell 1997;90:181–92.
  • PapkoffJ, Rubinfeld B, Schryver B, Polakis P. Wnt-I regulates free pools of catenins and stabilizes APC-catenin complexes. Mol Cell Biol 1996;16:2128–34.
  • Young C, Kitamura M, Mardy S, Kitajewski J. Wnt-I induces growth, cytosolic p-catenin, and Tcf/Lef transcriptional activation in Rat-1 fibroblast. Mol Cell Biol 1998;18:2474–85.
  • Hsu S, Galceran J, Grosschedl R. Modulation of transcriptional regulation by LEF-1 in response to Wnt-I signaling and association with p-catenin. Mol Cell Biol 1998;18: 4807–18.
  • Behrens J, von Kries JP, Kuhl M, Bruhn L, Wedlich D, Grosschedl R, et al. Functional interaction of p-catenin with the transcription factor LEF-1. Nature 1996;382:638–42.
  • Giese K, Cox J, Grosschedl R. The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of func-tional nucleoprotein structures. Cell 1992;69: 185–95.
  • Korinek V, Barker N, Morin PJ, van Wichen D, deWeger R, Kinzler K, et al. Constitutive transcriptional activation by a p-catenin-Tcf complex in APC(-/-) colon carcinoma. Science 1997;275:1784–7.
  • Tetsu 0, McCormick F. p-catenin regulates expression of cyclin D1 in colon carcinoma cells. Nature 1999;398: 422–6.
  • Yamagata N, Kobayashi K, Kasama T, Fukushima T, Tabata M, Yoneya I, et al. Multiple cytokine activities and loss of interleukin-2 inhibitor in synovial fluids of patients with rheumatoid arthritis. J Ftheumatol 1988;15:1623–7.
  • Shull MM, Kier AB, Diebold RJ, Yin M, Doetschman T. The importance of transforming growth factor p -1 in immunologicalhomeostasis, as revealed by gene ablation in mice. In: Jacob CO, 59. editor. Overexpression and knockout of cytokines in transgenic mice. San Diego: Academic Press; 1994. p. 135.
  • Butler DM, Piccoli DS, Hart PH, Hamilton JA. Stimulation of 60. human synovial fibroblast DNA synthesis by recombinant human cytokines. J Ftheumatol 1988;15:1463–70.
  • Kawakami A, Eguchi K, Matsuoka N, Tsuboi M, Kawabe Y, 61. Aoyagi T, et al. Inhibition of Fas antigen-mediated apoptosis of rheumatoid synovial cells in vitro by transforming growth factor3-1. Arthritis Rheum 1996;39: 1267–76.62.
  • Tsuboi M, Eguchi K, Kawakami A, Matsuoka N, Kawabe Y, Aoyagi T, et al. Fas antigen expression on synovial cells was down-regulated by interleukin-143. Biochem Biophys Res Commun1996;218:280-5.63.
  • Sen M, Lauterbach K, El-Gabalawy H, Firestein GS, Corr M, Carson DA. Expression and function of wingless and frizzled homologs in rheumatoid arthritis. Proc Natl Acad Sci USA 64. 2000;97:2791–6.
  • Sheldahl LC, Park M, Malbon CC, Moon RT. Protein kinase C is differentially stimulated by Wnt and frizzled homologs in aG-protein-dependent manner. Curr Biol 1999;9:695-8.65.
  • Washizu J, Nishimura H, Nakamura N, Nimura Y, Yoshikai Y. The NF-x-B binding site is essential for transcriptional activation of the IL-15 gene. Immunogenetics 1998;48: 1–7.
  • Anrather J, Csizmadia V, Soares MP, Winkler H. Regulation of NF-K-B RelA phosphorylation and transcriptional activity by p21 66.(ras) and protein kinasein primary endothelial cells. J BiolChem 1999;274:13594–603.
  • Cawston TE. Proteinase inhibitors. In: Barret AJ, Salvesen G, editors. Metalloproteinase inhibitors. Amsterdam: Elsevier; 1986. p. 589–610.
  • al-Ramadi BK, Meissler JJ Jr, Huang D, Eisenstein TK. Immunosuppression induced by nitric oxide and its inhibition by interleukin-4. Eur J Immunol 1992;22: 2249�54.
  • McCall TB, Palmer RM, Moncada S. Interleukin-8 inhibits the induction of nitric oxide synthase in rat peritoneal neutrophiles. Biochem Biophys Res Commun 1992;186: 680�5.
  • Gazzinelli RT, Oswald IP, James SL, Sher A. IL-10 inhibits parasite killing and nitrogen oxide production by IFN-�-activated macrophages. J Immunol 1992;148:1792�6.
  • Schini VB, Durante W, Elizondo E, Scott-Burden T, Junquero DC, Schafer AI, et al. The induction of nitric oxide synthase activity is inhibited by TGF--1, PDGF AB and PDGF BB in vascular smooth muscle cells. Eur J Pharmacol 1992;216: 379�83.
  • Tsujino M, Hirata Y, Imai T, Kanno K, Eguchi S, Ito H, et al. Induction of nitric oxide synthase gene by interleukin-1- in cultured rat cardiocytes. Circulation 1994;90:375�83.
  • Goureau O, Lepoivre M, Coutois Y. Lipopolysaccharides and cytokines induce a macrophage-type of nitric oxide synthase in bovine retinal pigmented epitherial cells. Biochem Biophys Res Commun 1992;186:854�9.
  • Szabo C, Zingarelli B, O�Connor M, Salzman AL. DNA strand breakage, activation of poly (ADP-ribose) synthetase, and cellular energy depletion are involved in the cytotoxicity in macrophages and smooth muscle cells exposed to peroxynitrite. Proc Natl Acad Sci USA 1996;93:1753�8.
  • Nguyen T, Brunston D, Crespi CL, Penman BW, Winshnok JS, Tannenbaum SR. DNA damage and mutation in human cells exposed to nitric oxide in vitro. Proc Natl Acad Sci USA 1992;89:3030�4.

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