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Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease

Using monoclonal antibody affinity chromatography, we isolated a 48,000 mol wt, glucose-rich glycoprotein (3M-1) from collagenase-solubilized rabbit renal tubular basement membrane (SRTA). The purified 3M-1 protein is noncollagenous, and is capable of inducing anti-TBM (tubular basement membrane) an...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187569/
https://www.ncbi.nlm.nih.gov/pubmed/3882878
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description Using monoclonal antibody affinity chromatography, we isolated a 48,000 mol wt, glucose-rich glycoprotein (3M-1) from collagenase-solubilized rabbit renal tubular basement membrane (SRTA). The purified 3M-1 protein is noncollagenous, and is capable of inducing anti-TBM (tubular basement membrane) antibodies and interstitial nephritis in susceptible hosts. Further, when SRTA, at a normally nephritogenic dose, was selectively depleted of 3M-1, it lost its ability to induce disease. As shown by immunofluorescent techniques, 3M-1 appears to be localized on rodent TBM to the exclusion of the glomerular basement membrane, but was lacking in the TBM of the LEW rat, a strain devoid of the relevant antigen of anti-TBM disease. Immunoelectron microscopy revealed that 3M- 1 was associated with the most lateral aspect of the TBM, which borders, and lies in the interstitium. These results indicate that 3M-1 is the nephritogenic antigen producing experimental anti-TBM disease.
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spelling pubmed-21875692008-04-17 Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease J Exp Med Articles Using monoclonal antibody affinity chromatography, we isolated a 48,000 mol wt, glucose-rich glycoprotein (3M-1) from collagenase-solubilized rabbit renal tubular basement membrane (SRTA). The purified 3M-1 protein is noncollagenous, and is capable of inducing anti-TBM (tubular basement membrane) antibodies and interstitial nephritis in susceptible hosts. Further, when SRTA, at a normally nephritogenic dose, was selectively depleted of 3M-1, it lost its ability to induce disease. As shown by immunofluorescent techniques, 3M-1 appears to be localized on rodent TBM to the exclusion of the glomerular basement membrane, but was lacking in the TBM of the LEW rat, a strain devoid of the relevant antigen of anti-TBM disease. Immunoelectron microscopy revealed that 3M- 1 was associated with the most lateral aspect of the TBM, which borders, and lies in the interstitium. These results indicate that 3M-1 is the nephritogenic antigen producing experimental anti-TBM disease. The Rockefeller University Press 1985-02-01 /pmc/articles/PMC2187569/ /pubmed/3882878 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
title Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
title_full Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
title_fullStr Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
title_full_unstemmed Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
title_short Isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
title_sort isolation and characterization of the nephritogenic antigen producing anti-tubular basement membrane disease
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187569/
https://www.ncbi.nlm.nih.gov/pubmed/3882878