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A small N-terminal 60-kD fragment of gp600 (megalin), the major autoantigen of active Heymann nephritis, can induce a full-blown disease.
Oleinikov, Andrew V; Feliz, Brady J; Makker, Sudesh P.
Afiliación
  • Oleinikov AV; Department of Pediatrics, Division of Nephrology, School of Medicine, University of California, Davis, California.
  • Feliz BJ; Department of Pediatrics, Division of Nephrology, School of Medicine, University of California, Davis, California.
  • Makker SP; Department of Pediatrics, Division of Nephrology, School of Medicine, University of California, Davis, California.
J Am Soc Nephrol ; 11(1): 57-64, 2000 Jan.
Article en En | MEDLINE | ID: mdl-10616840
Active Heymann nephritis of rat, an autoimmune glomerular disease, is an immunohistological, ultrastructural, and clinical model of human membranous glomerulonephritis. Both diseases in their full-blown form are characterized by (1) the formation of large, subepithelial glomerular immune deposits, which stain for IgG, C3, and membrane attack (C5b-9) components of complement and (2) the excretion of large amounts of protein in the urine (proteinuria). The target autoantigen of active Heymann nephritis is a large transmembrane renal glycoprotein with a molecular weight of approximately 600 kD, variously named gp600, gp330, LRP-2, or "megalin." This study was performed to identify the region in this enormously large glycoprotein that would produce full-blown active Heymann nephritis. A stable, small (60-kD) proteolytic fragment of gp600 was isolated and localized to the N-terminal end of the molecule using Western blot, sequencing, and amino acid analyses. Based on its primary structure, this fragment contains approximately 60 cysteine residues, the cross-linking of which to each other probably explains its stability. Immunization of rats with this fragment induced a full-blown disease that was comparable to the disease induced by a preparation containing the whole protein. These results indicate that this small fragment, retaining the natural disulfide bonds and probably its overall structure, contains those B and T cell epitopes that are sufficient to produce this organ-specific autoimmune disease.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Autoantígenos / Glicoproteínas de Membrana / Glomerulonefritis / Glomérulos Renales Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2000 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Autoantígenos / Glicoproteínas de Membrana / Glomerulonefritis / Glomérulos Renales Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2000 Tipo del documento: Article Pais de publicación: Estados Unidos