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. 1992 Mar 1;175(3):623–635. doi: 10.1084/jem.175.3.623

A nephritogenic rat monoclonal antibody to mouse aminopeptidase A. Induction of massive albuminuria after a single intravenous injection

PMCID: PMC2119147  PMID: 1740657

Abstract

Antibodies directed against antigens present on renal epithelial cells can cause membranous glomerulonephritis in experimental animals, which closely resembles the human form of this disease. However, most antibodies produced so far fail to cause the persistent and severe proteinuria that is seen in humans. In our search for new antibodies of this kind, we have now produced a monoclonal antibody (mAb) against mouse aminopeptidase A, a hydrolase that is present in the mouse kidney. The mAb (ASD-4) was prepared by fusion of mouse myeloma cells with splenocytes of Lou rats immunized with brush border (BB) membranes from mouse kidneys. ASD-4 is of the IgG1 subclass and reacts with a 140- kD protein as demonstrated by immunoprecipitation on radiolabeled BB membranes. In indirect immunofluorescence and immunoelectronmicroscopy of normal mouse kidneys, ASD-4 was diffusely present on the BB of the S1 and S2 segments of the proximal tubules, and on the cell membranes of the glomerular visceral epithelia. It also bound to cell membranes of nonglomerular endothelia, smooth muscle cells of arteries, and juxtaglomerular cells. After injection of ASD-4 into normal mice, an immediate homogeneous binding to the capillary wall was seen that gradually changed into a fine granular pattern after 1 d. This glomerular binding was followed by binding to the BB and basolateral membranes of the convoluted proximal tubules. Immediately after injection of ASD-4, a dose-dependent albuminuria occurred that lasted for at least 16 d. ASD-4 is thus a new rat mAb against a well-defined renal epithelial antigen that causes not only membranous glomerulonephritis after a single injection in the mouse, but also severe albuminuria.

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Selected References

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  1. Assmann K. J., Ronco P., Tangelder M. M., Lange W. P., Verroust P., Koene R. A. Comparison of antigenic targets involved in antibody-mediated membranous glomerulonephritis in the mouse and rat. Am J Pathol. 1985 Oct;121(1):112–122. [PMC free article] [PubMed] [Google Scholar]
  2. Assmann K. J., Ronco P., Tangelder M. M., Lange W. P., Verroust P., Koene R. A. Comparison of antigenic targets involved in antibody-mediated membranous glomerulonephritis in the mouse and rat. Am J Pathol. 1985 Oct;121(1):112–122. [PMC free article] [PubMed] [Google Scholar]
  3. Assmann K. J., Ronco P., Tangelder M. M., Lange W. P., Verroust P., Koene R. A. Involvement of an antigen distinct from the Heymann antigen in membranous glomerulonephritis in the mouse. Lab Invest. 1989 Jan;60(1):138–146. [PubMed] [Google Scholar]
  4. Assmann K. J., Tangelder M. M., Lange W. P., Schrijver G., Koene R. A. Anti-GBM nephritis in the mouse: severe proteinuria in the heterologous phase. Virchows Arch A Pathol Anat Histopathol. 1985;406(3):285–299. doi: 10.1007/BF00704298. [DOI] [PubMed] [Google Scholar]
  5. Assmann K. J., Tangelder M. M., Lange W. P., Tadema T. M., Koene R. A. Membranous glomerulonephritis in the mouse. Kidney Int. 1983 Sep;24(3):303–312. doi: 10.1038/ki.1983.159. [DOI] [PubMed] [Google Scholar]
  6. Bordier C. Phase separation of integral membrane proteins in Triton X-114 solution. J Biol Chem. 1981 Feb 25;256(4):1604–1607. [PubMed] [Google Scholar]
  7. Brentjens J. R., Andres G. Interaction of antibodies with renal cell surface antigens. Kidney Int. 1989 Apr;35(4):954–968. doi: 10.1038/ki.1989.79. [DOI] [PubMed] [Google Scholar]
  8. Campbell D. J. Circulating and tissue angiotensin systems. J Clin Invest. 1987 Jan;79(1):1–6. doi: 10.1172/JCI112768. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Coombs R. R., Scott M. L., Cranage M. P. Assays using red cell-labelled antibodies. J Immunol Methods. 1987 Jul 16;101(1):1–14. doi: 10.1016/0022-1759(87)90209-2. [DOI] [PubMed] [Google Scholar]
  10. Couser W. G. Mechanisms of glomerular injury in immune-complex disease. Kidney Int. 1985 Sep;28(3):569–583. doi: 10.1038/ki.1985.167. [DOI] [PubMed] [Google Scholar]
  11. Couser W. G. Mediation of immune glomerular injury. J Am Soc Nephrol. 1990 Jul;1(1):13–29. doi: 10.1681/ASN.V1113. [DOI] [PubMed] [Google Scholar]
  12. Dekan G., Miettinen A., Schnabel E., Farquhar M. G. Binding of monoclonal antibodies to glomerular endothelium, slit membranes, and epithelium after in vivo injection. Localization of antigens and bound IgGs by immunoelectron microscopy. Am J Pathol. 1990 Oct;137(4):913–927. [PMC free article] [PubMed] [Google Scholar]
  13. Douglas J. G. Angiotensin receptor subtypes of the kidney cortex. Am J Physiol. 1987 Jul;253(1 Pt 2):F1–F7. doi: 10.1152/ajprenal.1987.253.1.F1. [DOI] [PubMed] [Google Scholar]
  14. Dzau V. J., Burt D. W., Pratt R. E. Molecular biology of the renin-angiotensin system. Am J Physiol. 1988 Oct;255(4 Pt 2):F563–F573. doi: 10.1152/ajprenal.1988.255.4.F563. [DOI] [PubMed] [Google Scholar]
  15. Dzau V. J. Multiple pathways of angiotensin production in the blood vessel wall: evidence, possibilities and hypotheses. J Hypertens. 1989 Dec;7(12):933–936. doi: 10.1097/00004872-198912000-00001. [DOI] [PubMed] [Google Scholar]
  16. Fukatsu A., Yuzawa Y., Olson L., Miller J., Milgrom M., Zamlauski-Tucker M. J., Van Liew J. B., Campagnari A., Niesen N., Patel J. Interaction of antibodies with human glomerular epithelial cells. Lab Invest. 1989 Oct;61(4):389–403. [PubMed] [Google Scholar]
  17. Gossrau R. Peptidasen II. Zur Lokalisation der Dipeptidylpeptidase IV (DPP IV). Histochemische und biochemische Untersuchung. Histochemistry. 1979 Apr 3;60(2):231–248. doi: 10.1007/BF00495756. [DOI] [PubMed] [Google Scholar]
  18. Huang T. W., Langlois J. C. Podoendin. A new cell surface protein of the podocyte and endothelium. J Exp Med. 1985 Jul 1;162(1):245–267. doi: 10.1084/jem.162.1.245. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Katz A. M. Angiotensin II: hemodynamic regulator or growth factor? J Mol Cell Cardiol. 1990 Jul;22(7):739–747. doi: 10.1016/0022-2828(90)90086-h. [DOI] [PubMed] [Google Scholar]
  20. Kerjaschki D., Farquhar M. G. Immunocytochemical localization of the Heymann nephritis antigen (GP330) in glomerular epithelial cells of normal Lewis rats. J Exp Med. 1983 Feb 1;157(2):667–686. doi: 10.1084/jem.157.2.667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kerjaschki D., Farquhar M. G. The pathogenic antigen of Heymann nephritis is a membrane glycoprotein of the renal proximal tubule brush border. Proc Natl Acad Sci U S A. 1982 Sep;79(18):5557–5561. doi: 10.1073/pnas.79.18.5557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kerjaschki D., Sharkey D. J., Farquhar M. G. Identification and characterization of podocalyxin--the major sialoprotein of the renal glomerular epithelial cell. J Cell Biol. 1984 Apr;98(4):1591–1596. doi: 10.1083/jcb.98.4.1591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kugler P. Aminopeptidase A is angiotensinase A- I. Quantitative histochemical studies in the kidney glomerulus. Histochemistry. 1982;74(2):229–245. doi: 10.1007/BF00495833. [DOI] [PubMed] [Google Scholar]
  24. Kugler P. Aminopeptidase A is angiotensinase A. II. Biochemical studies on aminopeptidase A and M in rat kidney homogenate. Histochemistry. 1982;74(2):247–261. doi: 10.1007/BF00495834. [DOI] [PubMed] [Google Scholar]
  25. Kugler P. Localization of aminopeptidase A (angiotensinase A) in the rat and mouse kidney. Histochemistry. 1981;72(2):269–278. doi: 10.1007/BF00517140. [DOI] [PubMed] [Google Scholar]
  26. Kugler P., Schiebler T. H. Quantitative histochemistry of the angiotensinase A (APA) in the renal glomeruli of rats after stimulation of the renin-angiotensin system. Cytometry. 1984 Jul;5(4):392–395. doi: 10.1002/cyto.990050416. [DOI] [PubMed] [Google Scholar]
  27. Kugler P. Ultracytochemistry of aminopeptidase A (angiotensinase A) in the kidney glomerulus and juxtaglomerular apparatus. Histochemistry. 1982;74(2):199–212. doi: 10.1007/BF00495830. [DOI] [PubMed] [Google Scholar]
  28. Köhler G., Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature. 1975 Aug 7;256(5517):495–497. doi: 10.1038/256495a0. [DOI] [PubMed] [Google Scholar]
  29. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  30. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  31. Lojda Z., Gossrau R. Study on aminopeptidase A. Histochemistry. 1980;67(3):267–290. doi: 10.1007/BF00692761. [DOI] [PubMed] [Google Scholar]
  32. Malathi P., Preiser H., Fairclough P., Mallett P., Crane R. K. A rapid method for the isolation of kidney brush border membranes. Biochim Biophys Acta. 1979 Jun 13;554(1):259–263. doi: 10.1016/0005-2736(79)90023-3. [DOI] [PubMed] [Google Scholar]
  33. Mancini G., Carbonara A. O., Heremans J. F. Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry. 1965 Sep;2(3):235–254. doi: 10.1016/0019-2791(65)90004-2. [DOI] [PubMed] [Google Scholar]
  34. Markwell M. A. A new solid-state reagent to iodinate proteins. I. Conditions for the efficient labeling of antiserum. Anal Biochem. 1982 Sep 15;125(2):427–432. doi: 10.1016/0003-2697(82)90025-2. [DOI] [PubMed] [Google Scholar]
  35. Mendelsohn F. A., Dunbar M., Allen A., Chou S. T., Millan M. A., Aguilera G., Catt K. J. Angiotensin II receptors in the kidney. Fed Proc. 1986 Apr;45(5):1420–1425. [PubMed] [Google Scholar]
  36. Mendrick D. L., Rennke H. G. Induction of proteinuria in the rat by a monoclonal antibody against SGP-115/107. Kidney Int. 1988 Apr;33(4):818–830. doi: 10.1038/ki.1988.73. [DOI] [PubMed] [Google Scholar]
  37. Miettinen A., Dekan G., Farquhar M. G. Monoclonal antibodies against membrane proteins of the rat glomerulus. Immunochemical specificity and immunofluorescence distribution of the antigens. Am J Pathol. 1990 Oct;137(4):929–944. [PMC free article] [PubMed] [Google Scholar]
  38. Natori Y., Hayakawa I., Shibata S. Passive Heymann nephritis with acute and severe proteinuria induced by heterologous antibody against renal tubular brush border glycoprotein gp108. Lab Invest. 1986 Jul;55(1):63–70. [PubMed] [Google Scholar]
  39. Navar L. G., Rosivall L. Contribution of the renin-angiotensin system to the control of intrarenal hemodynamics. Kidney Int. 1984 Jun;25(6):857–868. doi: 10.1038/ki.1984.102. [DOI] [PubMed] [Google Scholar]
  40. Nishikawa K., Fukatsu A., Tamai H., Suzuki N., Ito Y., Sakamoto N., Matsuo S. Formation of subepithelial dense deposits in rats induced by a monoclonal antibody against the glomerular cell surface antigen. Clin Exp Immunol. 1991 Jan;83(1):143–148. doi: 10.1111/j.1365-2249.1991.tb05604.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Orikasa M., Matsui K., Oite T., Shimizu F. Massive proteinuria induced in rats by a single intravenous injection of a monoclonal antibody. J Immunol. 1988 Aug 1;141(3):807–814. [PubMed] [Google Scholar]
  42. Ozaki I., Ito Y., Fukatsu A., Suzuki N., Yoshida F., Watanabe Y., Sakamoto N., Matsuo S. A plasma membrane antigen of rat glomerular epithelial cells. Antigenic determinants involving N-linked sugar residues in a 140-kilodalton sialoglycoprotein of the podocytes. Lab Invest. 1990 Nov;63(5):707–716. [PubMed] [Google Scholar]
  43. Ronco P., Allegri L., Melcion C., Pirotsky E., Appay M. D., Bariety J., Pontillon F., Verroust P. A monoclonal antibody to brush border and passive Heymann nephritis. Clin Exp Immunol. 1984 Feb;55(2):319–332. [PMC free article] [PubMed] [Google Scholar]
  44. Salant D. J., Quigg R. J., Cybulsky A. V. Heymann nephritis: mechanisms of renal injury. Kidney Int. 1989 Apr;35(4):976–984. doi: 10.1038/ki.1989.81. [DOI] [PubMed] [Google Scholar]
  45. Tauc M., Chatelet F., Verroust P., Vandewalle A., Poujeol P., Ronco P. Characterization of monoclonal antibodies specific for rabbit renal brush-border hydrolases: application to immunohistological localization. J Histochem Cytochem. 1988 May;36(5):523–532. doi: 10.1177/36.5.2895788. [DOI] [PubMed] [Google Scholar]
  46. Verroust P., Ronco P., Chatelet F. Antigenic targets in membranous glomerulonephritis. Springer Semin Immunopathol. 1987;9(4):341–358. doi: 10.1007/BF00197213. [DOI] [PubMed] [Google Scholar]
  47. Wu Q., Lahti J. M., Air G. M., Burrows P. D., Cooper M. D. Molecular cloning of the murine BP-1/6C3 antigen: a member of the zinc-dependent metallopeptidase family. Proc Natl Acad Sci U S A. 1990 Feb;87(3):993–997. doi: 10.1073/pnas.87.3.993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Wu Q., Li L., Cooper M. D., Pierres M., Gorvel J. P. Aminopeptidase A activity of the murine B-lymphocyte differentiation antigen BP-1/6C3. Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):676–680. doi: 10.1073/pnas.88.2.676. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Yamada H., Sexton P. M., Chai S. Y., Adam W. R., Mendelsohn F. A. Angiotensin II receptors in the kidney. Localization and physiological significance. Am J Hypertens. 1990 Mar;3(3):250–255. doi: 10.1093/ajh/3.3.250. [DOI] [PubMed] [Google Scholar]
  50. Yoshioka T., Mitarai T., Kon V., Deen W. M., Rennke H. G., Ichikawa I. Role for angiotensin II in an overt functional proteinuria. Kidney Int. 1986 Oct;30(4):538–545. doi: 10.1038/ki.1986.219. [DOI] [PubMed] [Google Scholar]

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