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Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture

Human umbilical vein endothelial cells grown in vitro under standard conditions contain a high level of mRNA specific for the complement regulatory factors H and I. An additional 1.8-kb mRNA encoding a truncated form of factor H is also present. IFN-gamma stimulation of the cells causes a 6-7 fold i...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1988
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189095/
https://www.ncbi.nlm.nih.gov/pubmed/2972796
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collection PubMed
description Human umbilical vein endothelial cells grown in vitro under standard conditions contain a high level of mRNA specific for the complement regulatory factors H and I. An additional 1.8-kb mRNA encoding a truncated form of factor H is also present. IFN-gamma stimulation of the cells causes a 6-7 fold increase in both factor H mRNA species, and a greater than 10-fold increase in factor I mRNA. IL-1 and LPS slightly suppressed factor H mRNA, while TNF had no effect. mRNA for factor B is also detectable in IFN-gamma-stimulated cells, but messengers for C1q, C4bp, and CR3 beta chain were not found. Secretion of factor H protein was also stimulated by IFN-gamma. The presence of mRNA for factors H, B, and I, together with C3 secretion, demonstrated by others, suggests that endothelial cells can assemble the complete alternative complement pathway. Endothelial cell complement may be involved in leukocyte- endothelium interactions mediated by leukocyte C3 receptors.
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spelling pubmed-21890952008-04-17 Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture J Exp Med Articles Human umbilical vein endothelial cells grown in vitro under standard conditions contain a high level of mRNA specific for the complement regulatory factors H and I. An additional 1.8-kb mRNA encoding a truncated form of factor H is also present. IFN-gamma stimulation of the cells causes a 6-7 fold increase in both factor H mRNA species, and a greater than 10-fold increase in factor I mRNA. IL-1 and LPS slightly suppressed factor H mRNA, while TNF had no effect. mRNA for factor B is also detectable in IFN-gamma-stimulated cells, but messengers for C1q, C4bp, and CR3 beta chain were not found. Secretion of factor H protein was also stimulated by IFN-gamma. The presence of mRNA for factors H, B, and I, together with C3 secretion, demonstrated by others, suggests that endothelial cells can assemble the complete alternative complement pathway. Endothelial cell complement may be involved in leukocyte- endothelium interactions mediated by leukocyte C3 receptors. The Rockefeller University Press 1988-11-01 /pmc/articles/PMC2189095/ /pubmed/2972796 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
Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
title Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
title_full Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
title_fullStr Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
title_full_unstemmed Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
title_short Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
title_sort interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189095/
https://www.ncbi.nlm.nih.gov/pubmed/2972796