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Original Article

IgM Natural Autoantibodies Against Bromelain-Treated Mouse Red Blood Cells Recognise Carbonic Anhydrase

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Pages 207-216 | Received 29 Aug 1990, Accepted 13 Dec 1990, Published online: 07 Jul 2009

References

  • Cunningham A J. Self tolerance maintained by active suppressor mechanisms. Transplant Rev 1976; 31: 23–43
  • Steele E J, Cunningham A J. High proportion of Ig-producing cells making autoantibody in normal mice. Nature 1978; 274: 483–484
  • Cunningham A J. Large numbers of cells in normal mice produce antibody components of isologous erythrocytes. Nature 1974; 252: 749–751
  • Cunningham A J. Active suppressor mechanism maintaining tolerance to some self components. Nature 1975; 254: 143–144
  • Cunliffe D A, Cox K O. IgM-autoantibodies against isologous erythrocytes also react with isologous IgG (Fc). Nature 1980; 286: 720–722
  • Cunningham A J, Steele E J. Ontogeny of the autoimmune reaction in normal mice to antigens in erythrocytes and gut. Clin exp Immunol 1981; 44: 38–48
  • Serban D, Pages J M, Bussard A E, Witz I P. The participation of trimethylammonium in the mouse erythrocyte epitope recognised by monoclonal autoantibodies. Immunol Letts 1981; 3: 315–319
  • Pages J, Poncet P, Serban D, Witz I, Bussard A E. Relationship between choline derivatives and mouse erythrocyte membrane antigens revealed by mouse monoclonal antibodies. I. Anticho-line activity of anti-mouse erythrocyte monoclonal antibodies. 1mm Letts 1982; 5: 167–173
  • Poncet P, Kocher H P, Pages J, Jaton J C, Bussard A E. Monoclonal antibodies against mouse red blood cells: A family of structurally restricted molecules. Molecular Immunol 1985; 22: 541–551
  • Serban D, Witz I P. Further studies on the determinant recognised by naturally-occurring murine autoantibodies reacting with bromelain-treated erythrocytes. Immunol Lett 1988; 18: 191–200
  • Cox K O, Hardy S J. Autoantibodies against mouse bromelain-modified RBC are specifically inhibited by a common membrane phospholipid, phosphatidylcholine. Immunology 1985; 55: 263–271
  • Kawaguchi S. Phospholipid epitopes for mouse antibodies against bromelain-treated mouse erythrocytes. Immunology 1987; 62: 11–16
  • Mercolino T J, Arnold L W, Haughton G. Phosphatidylcholine is recognised by a series of Ly-l+murine B cell lymphomas specific for erythrocyte membranes. J exp Med 1986; 163: 155–165
  • Mercolino T J, Arnold L W, Hawkins L A, Haughton G. Normal mouse peritoneum contains a large population of Ly-1+(CD5) B-cells that recognise phosphatidylcholine. Relationship to cells that secrete hemolytic antibody specific for autologous erythrocytes. J exp Med 1988; 168: 687–698
  • Jonusys A M, Steele E J. IgM anti-erythrocyte autoantibodies specific for buried and neo-antigens using cellular-ELISA assays. Mol Immunol 1988; 25: 535–543
  • Laemmti U K. Cleavage of the structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 227: 680
  • Neuhoff V, Arold N, Taube D, Ehrhardt W. Improved staining of proteins in polyacrylamide gels including isoelectric focusing gels with clear background at nanogram sensitivity using Coomassie Brilliant Blue G-250 and R-250. Electrophoresis 1988; 9: 255–262
  • Wardi A H, Michos G A. Anal Biochem 1972; 49: 607
  • Sarris A H, Palade G E. The sialoglycoproteins of murine erythrocyte ghosts. J Biol Chem 1979; 254: 6724–6731
  • Towbin H, Staehelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose. Proc Natl Acad Sci USA 1979; 76: 4350
  • Leary J J, Brigati D J, Ward D C. Rapid and sensitive colori-metric method for visualizing biotin-labeled DNA probes hybridized to DNA and RNA immobilized on nitrocellulose: Bioblots. Proc Natl Acad Sci USA 1983; 80: 4050–4059
  • Carlsson U, Henderson L E, Lindskog S. Denaturation and reactivation of human carbonic anhydrases in guanidine hydrochloride and urea. BBA 1973; 310: 376–87
  • Pages J, Bussard A E. Precommitment of normal mouse peritoneal cells by erythrocyte antigens in relation to autoantibody production. Nature 1975; 25: 316
  • Pages J, Arnaud D. Visualization of erythrocyte membrane antigen by means of fluorescent microspheres coupled to monoclonal mouse auto-antibody: Distribution of this antigen among species. lmm Lett 1980; 8: 7–13
  • Laing P, Appleby L A, Culbert E J, Elson C J. Antigenicity of rat erythrocyte glycophorins. lmm Lett 1988; 18: 125–128
  • Garzelli C, Basolo F, Puglisi C, Pacciardi A. Multiple organ-reactivity of monoclonal autoantibodies to mouse erythrocytes. Experientia 1987; 43: 912–914
  • Tashian R E. The carbonic anhydrases: Widening perspectives on their evolution, expression and function. Bioessays 1989; 10: 186–192
  • Landsverk T, Jansson A, Nicander L, Ploen L. Carbonic anhydrase - a marker for particles shed from the epithelium to the lymphoid follicles of the ileal Peyer's patch in goat kids and lambs. Immunol Cell Biol 1987; 65: 425–9
  • Spicer S S, Stoward P J, Tashian R E. The immunohistolocaliz-ation of carbonic anhydrase in rodent tissues. J Histochem Cytochem 1979; 27: 820–831
  • Eicher E M, Stern R H, Womack J E, Davisson M T, Roderick T H, Reynolds S C. Evolution of the mammalian carbonic anhydrase loci by tandem duplication: Close linkage of the Car-l and Car-2 to the cetromere region of chromosome 3 of the mouse. Biochem Genetics 1976; 14: 651–660
  • Curtis P J. Cloning of mouse carbonic anhydrase mRNA and its induction in mouse erythroleukemic cells. J Biol Chem 1983; 258: 4459–4463
  • Curtis P J, Withers E, Demuth D, Watt R, Venta P J, Tashian R E. The nucleotide sequence and derived amino acid sequence of cDNA coding for the mouse carbonic anhydrase II. Gene 1983; 25: 325–332
  • Venta P J, Montgomery J C, Hewett-Emmett D, Wiebauer K, Tashian R E. Structure and exon to protein domain relationships of the mouse carbonic anhydrase II gene. J Biol Chem 1985; 260: 12130–12135
  • Deutsch H F. Carbonic anhydrases. Int Biochem 1987; 19: 101–113
  • Varga J M, Konigsberg W H, Richards F F. Antibodies with multiple binding functions. Induction of single immunoglobin species by structurally dissimilar haptens. Proc Natl Acad Sci USA 1973; 70: 3269–3274

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