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Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes

Short-term cultures of human peripheral blood monocytes were shown to synthesize the alternative pathway complement components C3, factors B (B) and D (D), and properdin, the regulatory proteins C3b inactivator (C3bINA) and beta 1H, in addition to C2, C4, and C5. B, D, properdin, C3bINA, and C2 were...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1980
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185797/
https://www.ncbi.nlm.nih.gov/pubmed/6444659
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description Short-term cultures of human peripheral blood monocytes were shown to synthesize the alternative pathway complement components C3, factors B (B) and D (D), and properdin, the regulatory proteins C3b inactivator (C3bINA) and beta 1H, in addition to C2, C4, and C5. B, D, properdin, C3bINA, and C2 were detected by functional assays, whereas beta 1H, C4, C3, and C5 could only be detected using immunochemical procedures. Immunoperoxidase localization studies showed that all the cells in each culture contained each component, so it is possible that all monocytes synthesize each component. It is concluded that cells of the monocyte- macrophage series form a mobile source of complement components and regulatory proteins which can be concentrated at sites of inflammation.
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spelling pubmed-21857972008-04-17 Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes J Exp Med Articles Short-term cultures of human peripheral blood monocytes were shown to synthesize the alternative pathway complement components C3, factors B (B) and D (D), and properdin, the regulatory proteins C3b inactivator (C3bINA) and beta 1H, in addition to C2, C4, and C5. B, D, properdin, C3bINA, and C2 were detected by functional assays, whereas beta 1H, C4, C3, and C5 could only be detected using immunochemical procedures. Immunoperoxidase localization studies showed that all the cells in each culture contained each component, so it is possible that all monocytes synthesize each component. It is concluded that cells of the monocyte- macrophage series form a mobile source of complement components and regulatory proteins which can be concentrated at sites of inflammation. The Rockefeller University Press 1980-03-01 /pmc/articles/PMC2185797/ /pubmed/6444659 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
Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
title Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
title_full Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
title_fullStr Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
title_full_unstemmed Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
title_short Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
title_sort biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185797/
https://www.ncbi.nlm.nih.gov/pubmed/6444659