Skip to main content
British Journal of Experimental Pathology logoLink to British Journal of Experimental Pathology
. 1987 Aug;68(4):527–538.

An assessment of the influence of antigen dose in two new models of chronic serum sickness glomerulonephritis in the rat.

P N Furness 1, D R Turner 1
PMCID: PMC2013136  PMID: 3651324

Abstract

Two new models of chronic serum sickness glomerulonephritis have been developed and characterized, using cationic and native bovine serum albumin (BSA). During this development, it has become apparent that there exists an optimum nephritogenic dose for native (anionic) BSA, above which the severity of glomerular changes diminishes; but for cationic BSA, higher doses consistently produce more severe lesions. This finding supports the theory that antigens of different charge are deposited in the glomerulus by different mechanisms. We have also found that cationic BSA circulates not in the blood plasma, but mainly bound to red cells. The two experimental models have proved to be more convenient and more consistent than those previously reported; the cationic BSA model also induces heavy proteinuria and the nephrotic syndrome. They will facilitate further studies of how antigen-antibody complexes are handled by the glomerulus in chronic immune complex disease.

Full text

PDF
527

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adler S. G., Wang H., Ward H. J., Cohen A. H., Border W. A. Electrical charge. Its role in the pathogenesis and prevention of experimental membranous nephropathy in the rabbit. J Clin Invest. 1983 Mar;71(3):487–499. doi: 10.1172/JCI110793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ambler J., Walker G. Isoelectric focusing of serum proteins on modified thin cellulose-acetate membranes. Clin Chem. 1979 Jul;25(7):1320–1322. [PubMed] [Google Scholar]
  3. Batsford S. R., Takamiya M., Vogt A. A model of in situ immune complex glomerulonephritis in the rat employing cationized ferritin. Clin Nephrol. 1980 Nov;14(5):211–216. [PubMed] [Google Scholar]
  4. Border W. A., Kamil E. S., Ward H. J., Cohen A. H. Antigenic changes as a determinant of immune complex localization in the rat glomerulus. Lab Invest. 1981 Nov;45(5):442–449. [PubMed] [Google Scholar]
  5. Border W. A., Ward H. J., Kamil E. S., Cohen A. H. Induction of membranous nephropathy in rabbits by administration of an exogenous cationic antigen. J Clin Invest. 1982 Feb;69(2):451–461. doi: 10.1172/JCI110469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cornacoff J. B., Hebert L. A., Smead W. L., VanAman M. E., Birmingham D. J., Waxman F. J. Primate erythrocyte-immune complex-clearing mechanism. J Clin Invest. 1983 Feb;71(2):236–247. doi: 10.1172/JCI110764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Danon D., Goldstein L., Marikovsky Y., Skutelsky E. Use of cationized ferritin as a label of negative charges on cell surfaces. J Ultrastruct Res. 1972 Mar;38(5):500–510. doi: 10.1016/0022-5320(72)90087-1. [DOI] [PubMed] [Google Scholar]
  8. Hoare D. G., Koshland D. E., Jr A method for the quantitative modification and estimation of carboxylic acid groups in proteins. J Biol Chem. 1967 May 25;242(10):2447–2453. [PubMed] [Google Scholar]
  9. Latta H., Fligiel S. Mesangial fenestrations, sieving, filtration, and flow. Lab Invest. 1985 Jun;52(6):591–598. [PubMed] [Google Scholar]
  10. Mannik M., Striker G. E. Removal of glomerular deposits of immune complexes in mice by administration of excess antigen. Lab Invest. 1980 May;42(5):483–489. [PubMed] [Google Scholar]
  11. Miyazaki S., Kawasaki K., Yaoita E., Yamamoto T., Kihara I. Bovine serum albumin (BSA) nephritis in rats. III. Antigen distribution in various organs. Clin Exp Immunol. 1985 Feb;59(2):293–299. [PMC free article] [PubMed] [Google Scholar]
  12. Miyazaki S., Kawasaki K., Yaoita E., Yamamoto T., Kihara I. Bovine serum albumin nephritis in rats. V. Kinetic studies of antigen localization in various organs and the phagocytic role of polymorphonuclear leukocytes. Am J Pathol. 1985 Jun;119(3):412–419. [PMC free article] [PubMed] [Google Scholar]
  13. Oite T., Shimizu F., Suzuki Y., Vogt A. Ultramicroscopic localization of cationized antigen in the glomerular basement membrane in the course of active, in situ immune complex glomerulonephritis. Virchows Arch B Cell Pathol Incl Mol Pathol. 1985;48(2):107–118. doi: 10.1007/BF02890120. [DOI] [PubMed] [Google Scholar]
  14. Schifferli J. A., Ng Y. C., Peters D. K. The role of complement and its receptor in the elimination of immune complexes. N Engl J Med. 1986 Aug 21;315(8):488–495. doi: 10.1056/NEJM198608213150805. [DOI] [PubMed] [Google Scholar]
  15. Vogt A., Rohrbach R., Shimizu F., Takamiya H., Batsford S. Interaction of cationized antigen with rat glomerular basement membrane: in situ immune complex formation. Kidney Int. 1982 Jul;22(1):27–35. doi: 10.1038/ki.1982.128. [DOI] [PubMed] [Google Scholar]
  16. Yamamoto T., Kihara I., Hara M., Kawasaki K., Yaoita E. Bovine serum albumin (BSA) nephritis in rats II. Histological findings and complement activation by immune complex in SHR rats. Br J Exp Pathol. 1983 Dec;64(6):660–669. [PMC free article] [PubMed] [Google Scholar]

Articles from British journal of experimental pathology are provided here courtesy of Wiley

RESOURCES