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pubmed-article:17869127pubmed:abstractTextThe IL-6 is a typical pleiotropic cytokine, which regulates T cell response, B cell differentiation and immunoglobulin production. Endothelial cells can produce large amounts of IL-6. SNP at position -174 (G/C) in the IL-6 promoter region was found to be associated with a series of complex diseases. In this study we analyzed whether IL-6 -174 G/C polymorphism has any effect on IL-6 production of in vitro cultured HUVECs. Thirty-three fresh umbilical cords were recruited from healthy pregnancies. The endothelial cells isolated from human umbilical cords were genotyped for IL-6 -174 SNP. C allele frequency was 0.379. The IL-6 production of each primary HUVEC line was measured after IL-1beta or LPS treatment by ELISA. Serial dilutions of the stimulating agents were applied and maximum amount of produced IL-6 (R(max)) and stimulator concentrations at half-maximal IL-6 response (MR(50)) were calculated for each of the cell lines. IL-6 production was not associated with IL-6 -174 SNP genotypes or with presence of C allele. Our results showed that IL-6 production of HUVEC after proinflammatory stimulation was not influenced by IL-6 -174 SNP. Further functional studies are required to compare differences and similarities in IL-6 -174 SNP dependent expression of IL-6 among various cell types.lld:pubmed
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pubmed-article:17869127pubmed:authorpubmed-author:MakóVeronikaVlld:pubmed
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pubmed-article:17869127pubmed:pagination17-22lld:pubmed
pubmed-article:17869127pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:17869127pubmed:year2007lld:pubmed
pubmed-article:17869127pubmed:articleTitleInterleukin-6 -174 promoter polymorphism does not influence IL-6 production after LPS and IL-1 beta stimulation in human umbilical cord vein endothelial cells.lld:pubmed
pubmed-article:17869127pubmed:affiliation3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.lld:pubmed
pubmed-article:17869127pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17869127pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:17869127pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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