10
Views
3
CrossRef citations to date
0
Altmetric
Original Article

Antibodies to a Microbial Peptide Sharing Sequence Homology with βA3-Crystallin Damage Lens Epithelial Cells in vitro and in viva

, , , , , , & show all
Pages 311-322 | Received 02 Jul 1998, Published online: 07 Jul 2009

References

  • Guggenmoos-Holzmann I., Engel B., Henke V., Naumann G. O.H. Cell density of human lens epithelium in women higher than in man. Invest. Ophthalmol. Vis. Sci. 1989; 30: 330
  • Konofsky K., Naumann G. O.H., Guggenmoos-Holzmann I. Cell densitysex chromatin in lens epithelium of human cataracts. Ophthalmology 1987; 94: 875
  • Straatsma B. R, Lightfoot D. O, Barke R. M., , Horwitz J, et al. Lens capsuleepithelium in age-related cataract. Am. J. Ophthalmol. 1991; 112: 283
  • Fagerholm P. P., , Philipson B. T, et al. Human lens epithelium in normalcataractous lenses. Invest. Ophthalmol. Vis. Sci. 1981; 21: 408
  • Streeten B. W., , Eshaghian J, et al. Human posterior subcapsular cataract. A grossflat preparation study. Arch. Ophthalmol. 1978; 96: 16530
  • von Sallmann L. The lens epithelium in the pathogenesis of cataract. Am. J. Ophthalmol. 1957; 44: 159
  • Saitoh J., Nishi O., Hitani H. Cell densityhexagonality of lens epithelium in human cataracts. Nippon Ganka Gakkai Zasshi 1990; 94: 176
  • Singh D. P, Guru S. C, Kikuchi T., Abe T., Shinohara T. Autoantibodies against β-crystallins induce lens epithelial cell damagecataract formation in mice. J. Immunol. 1995; 155: 993
  • Angunawela I. I. The role of autoimmune phenomena in the pathogenesis of cataract. Immunology 1987; 61: 363
  • Angunawela I. I. The effect of immunosuppression on the development of experimental cataract. Immunology 1988; 64: 69
  • Ogha H., Katayama T., Egi K., Fujiwara H. (1990) Proceedings of the 5th International Symposium on the Immunology und Immunopathology of the Eye, Tokyo, March, 1990. Elsevier Science Publishers, Amsterdam, 13–15, 391–394
  • Patel M., Shine B., Murray P. I. Antilens antibodies in cataractinflammatory eye disease, an evolution of a new technique. Invest. Ophthalmol. Vis. Sci. 1990; 14: 97
  • Nissen S. H, Andersen P., Andersen H. M.K. Antibodies to lens antigens in cataractafter cataract surgery. Br. J. Ophthalmol. 1981; 65: 63
  • Sandberg H. O., , Closs O, et al. The humoral immune response to alpha, betagamma crystallins of the human lens. Scand. J. Immunol. 1979; 10: 549
  • D'Ermo F., Secchi H. Phospholipase Alysophosphatidylcholine in the pathogenesis of “permeability cataracts”. Klin Monatsbl Augenheilk 1977; 170: 433
  • Merck K. B, de Haard-Hoekman W. A, Cruysberg H., Bloemendal H., de Jong W. W. Characterization of anti-crystallin autoantibodies in patients with cataract. Mol. Biol. Rep. 1993; 17: 93
  • Manski W., Halbert S. P., , Javier P, et al. Comparison of rabbit antilens antibodies induced by iso-and hetero-immunization. Ann. N. Y. Acad. Sci. 1965; 124: 352
  • Okamura M. Age-related changes in the rat lens, morphologicalmorphometric studies. Nippon Ganka Gakkai Zasshi. 1991; 95: 209
  • Luntz M. H. Anti-wealanti-lens antibodies in uveitistheir significance. Exp. Eye Res. 1968; 7: 561
  • Chylack L. T., Jr, Wolfe J. K, Singer D. M, Leske M. C, Bullimore M. A, Bailey I., Friend J., McCarthy D., Wu S.-Y. The lens opacities classification system III. Arch. Ophthalmol. 1993; 111: 831
  • Chylack L. T., Jr, Singh D. P, Kikuchi T., Sueno T., Wolfe J., Shinohara T. Human sera obtained from patients with cataract killed lens epithelial cells in culture. Invest. Ophthlmol. Vis. Sci. Suppl. 1996; 37(3)S1142
  • Goldschmid L., Goldbaum M., Walker S. M., Weigle W. O. The immune response to homologous lens crystallin. I. Antibody production after lens injury. J. Immunol. 1982; 129: 1652
  • Rahi A. H.S., Misra R. H., Morgan G. Immunopathology of the lens, I. Humoralcellular immune responses to heterologous lens antigenstheir roles in ocular inflammation. Br. J. Ophthalmol. 1977; 61: 164
  • Secchi A. G, De Caro G., Togno G. S., Fregona I. A. Ultra microscopy of the lens in the course of experimental allergic uveitis. Ocular Immunology Today, M. Usui, S. Ohno, A. Aoki. Elsevier Science Publishers, Amsterdam 1990; 161
  • Ishimoto S., Sanui H., Ishibashi T., Inomata H. Experimental lens-induced granulomatous endophthalmitis in guinea pigs. Ocular Immunology Today, M. Usui, S. Ohno, A. Aoki. Elsevier Science Publishers, Amsterdam 1990; 161
  • Flugel G., Liebe S., Vooter C., Bloemendal H., Lutjen-Drecol E. Distribution of αB-crystallin in the anterior segment of primatebovine eyes. Curr. Eye Res. 1993; 12: 871
  • Bhat S. P., Nagineni C. N. αB subunit of lens-specific protein α-crystallin is present on other ocularnon-ocular tissues. Biochem. Biophys. Res. Com. 1989; 158: 313
  • Dubin R. M, Wawrousek E. F., , Piatigorsky J, et al. Expression of the murine αB-crystallin gene is not restricted to the lens. Mol. Cell. Biol. 1989; 9: 1083
  • Kato K., Shinohara H., Kurobe N., Goto S., Inaguma Y., Oshima K. Immunoreactive αA-crystallin in rat non-lenticular tissues detected with sensitive immunoassay method. Biochem. Biophys. Acta 1991; 1080: 173
  • Iwaki T., Iwaki A., Liem R. K.H., Goldman J. F. Expression of αB-crystallin in the developing rat kidney. Kid. Inter. 1991; 40: 52
  • Head M. W, Peter A., Clyton R. M. Evidence for the extra lenticular expression of members of the β-crystallin gene family in the chicka comparison with δ-crystallin during differentiationtransdifferentiation. Differentiation 1991; 48: 147
  • Zigler S., Jr, Sidbury J. B. A compurative study of β-crystallin from in six animals. Camp. Biochem. Physiol. 1976; 53B: 349
  • Bradford M. M. A rapid sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal. Biochem. 1976; 72: 248
  • Ausubel F. M, Brent R., Kingston R. E, Moore D. D, Seidman J. G, Smith J. A., , Struhl K, et al. Current Protocols in Molecular Biology. John WileySon, New York 1987; vol. 2: 10.1.1–10.1.3
  • Ibaraki N., Lin L.-R., Dang L., Reddy V. N, Singh T., Sueno T., Chylack L. T., Jr, , Shinohara T, et al. Age-related cataract, antibody against, β-crystallin or human sera isolated from catarcat patients killed lens epithelial cell. in vitro. Exp. Eye Res. 1997; 6: 229
  • Usukura J., Bok D. Changes in the localizationcontent of opsin during retinal development in the rds mutant mouse, immunocytochemistryimmunology. Exp. Eye Res. 1987; 45: 501
  • Hogg D., Tsui L.-C., Gorin M., Breitman I. M. Characterization of the human β-crystallin gene HuβA3/ A1 reveals ancestral relationships among the beta gamma-crystallin superfamily. J. Bid. Chem. 1986; 15: 12420
  • Kaneshisa M. Integrated DatabaseExtended Analysis System, for Nucleic AcidProtein. National Cancer Institute, Frederick, MD 1987
  • Lai J. C, Fukushima A., Wawrousek E. F, Lobanoff P., Charukamnoetknok P., Smith-Gill S. J, Vistica B. P, Lee R. S, Egwuagu C. E, Whitcup S. M., Gery I. Immunotolerance against a foreign antigen transgenetically expressed in the lens. Invest. Ophthalmol. Vis. Sci. 1998; 39: 2049
  • Kabat E. A. Structural Concept in ImmunologyImmunochemistry 2nd edn. Holt RinehartWinston, New York 1976
  • Inana G., Piatigorsky J., Norman B., Slingsby C., Blundell T. Geneprotein structure of a β-crystallin polypeptide in murine lens, relationship of exonsstructural motifs. Nature 1983; 302: 310
  • David L. L., Shearer T. R. β-crystallin in solubilized by calpain II in vitro contain cleavage sites similar to β-crystallins in solubilized during cataract. FEBS lett. 1993; 324: 265
  • Eto K., Suzuki S., Singh V. K., Shinohara T. Immunization with recombinant Escherichia coli expressing retinal S-antigen-induced experimental autoimmune uveitis (EAU) in Lewis rats. Cell. Immunol. 1993; 147: 203
  • Sunil S., Eto K., Singh V. K., Shinohara T. Oligopeptides of three to five residues derived from uveitopathogenic sites of retinal S-antigen induce experimental autoimmune uveitis (EAU) in Lewis rats. Cell. Immunol. 1993; 148: 198
  • Singh D. P, Kikuchi T., Singh V. J., , Shinohara T, et al. A single amino acid substitution in core residues of S-antigen prevents experimental autoimmune uveitis. J. Immunol. 1994; 152: 4699
  • Spector A. Aspects of the biochemistry of cataract. The Ocular Lens, H. Maisel. Marcel Dekker, Inc., New York 1985; 405
  • Zigler J. S., Jr, Huang Q. L., , Du X. Y, et al. Oxidative modification of lens crystallin by H2O2chelated iron. Free Radic. Biol. Med. 1989; 7: 499
  • Ortwerth B. J., , Olesen P. R, et al. Ascorbic acid-induced crosslinking of lens protein, Evidence supporting a Maillard reaction. Biochim. Biophys. Acta 1988; 956: 10
  • Harding J. J., Crabbe M. J. The lens, development, proteins, metabolismcataract. The Eye3rd edn, H. Davson. Academic Press, NY 1984; 207–370
  • Harding J. J, Beswick H. T, Ajiboye R., Huby R., Blakytny R., Rixon K. G. Non-enzymatic post-translational modification of protein in aging. A review. Mech. Aging Dev. 1989; 50: 7
  • Kinoshita J. H. A thirty year journey in the polyol pathway. Exp. Eye Res. 1990; 50: 567
  • Ishimoto C., Goalwin P. W, Sun S.-T., Nishio I., Tanaka T. Cytoplasmic phase separation in formation of galactosemic cataract in lenses of young rats. Proc. Natl. Acad. Sci. USA 1979; 76: 4414

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.