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Connective tissue origin of the amyloid-related protein SAA

Protein SAA is a serum protein related to the major constituent of secondary amyloid fibrils, protein AA, and has been suggested to be a precursor of the amyloid protein AA. In the present study, the origin of SAA was investigated by studying human fetal tissues and cultured human fetal fibroblasts...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1976
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190449/
https://www.ncbi.nlm.nih.gov/pubmed/792382
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collection PubMed
description Protein SAA is a serum protein related to the major constituent of secondary amyloid fibrils, protein AA, and has been suggested to be a precursor of the amyloid protein AA. In the present study, the origin of SAA was investigated by studying human fetal tissues and cultured human fetal fibroblasts with the indirect immunofluorescence technique. Anti-SAA antibodies reacted strongly with cultured fibroblasts producing a fine fibrillary cytoplasmic staining and with extracellular fibrils in loose connective tissues and vessel walls. The reactions were specifically inhibited by absorption with degraded amyloid material, isolated protein AA, isolated protein SAA, and sera from patients with elevated levels of SAA. In contrast, no inhibition was seen with amyloid fibril material devoid of AA protein or by human sera in which SAA was not detectable by double-diffusion tests. These observations showed that SAA-like material is produced by fibroblasts and indicate that it is a normal constituent of developing extracellular connective tissue fibers.
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spelling pubmed-21904492008-04-17 Connective tissue origin of the amyloid-related protein SAA J Exp Med Articles Protein SAA is a serum protein related to the major constituent of secondary amyloid fibrils, protein AA, and has been suggested to be a precursor of the amyloid protein AA. In the present study, the origin of SAA was investigated by studying human fetal tissues and cultured human fetal fibroblasts with the indirect immunofluorescence technique. Anti-SAA antibodies reacted strongly with cultured fibroblasts producing a fine fibrillary cytoplasmic staining and with extracellular fibrils in loose connective tissues and vessel walls. The reactions were specifically inhibited by absorption with degraded amyloid material, isolated protein AA, isolated protein SAA, and sera from patients with elevated levels of SAA. In contrast, no inhibition was seen with amyloid fibril material devoid of AA protein or by human sera in which SAA was not detectable by double-diffusion tests. These observations showed that SAA-like material is produced by fibroblasts and indicate that it is a normal constituent of developing extracellular connective tissue fibers. The Rockefeller University Press 1976-11-02 /pmc/articles/PMC2190449/ /pubmed/792382 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
Connective tissue origin of the amyloid-related protein SAA
title Connective tissue origin of the amyloid-related protein SAA
title_full Connective tissue origin of the amyloid-related protein SAA
title_fullStr Connective tissue origin of the amyloid-related protein SAA
title_full_unstemmed Connective tissue origin of the amyloid-related protein SAA
title_short Connective tissue origin of the amyloid-related protein SAA
title_sort connective tissue origin of the amyloid-related protein saa
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190449/
https://www.ncbi.nlm.nih.gov/pubmed/792382