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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >SiRNA down-regulation of FGA mRNA in HepG2 cells demonstrated that heterozygous abnormality of the Aα-chain gene does not affect the plasma fibrinogen level
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SiRNA down-regulation of FGA mRNA in HepG2 cells demonstrated that heterozygous abnormality of the Aα-chain gene does not affect the plasma fibrinogen level

机译:SiRNA下调HepG2细胞中FGA mRNA的表达证明Aα链基因的杂合异常不会影响血浆纤维蛋白原水平

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Introduction We encountered two afibrinogenemia patients with homozygous and compound heterozygous FGA mutation. Of interest, the patients' parents, who are heterozygous, had normal levels of plasma fibrinogen; thus, we hypothesized that liver FGA mRNA levels were higher than those of FGB and/or FGG mRNA. Materials and Methods To test the hypothesis, we quantitated mRNA levels of a normal liver and a human hepatocyte cell line, HepG2 cells, and performed siRNA-mediated down-regulation of the fibrinogen gene in HepG2 cells. mRNA levels were determined using real-time quantitative RT- PCR for three normal livers and HepG2 cells. Down-regulation of FGA, FGB, or FGG in HepG2 cells was performed by the addition of siRNA corresponding to each of the three genes, and the mRNA levels determined in the cells and the secreted fibrinogen concentration in media. Results The mRNA level of normal human liver was FGA = FGB > FGG and the FGG mRNA level was about 2-fold lower than the others, that of HepG2 cells was FGA > FGG > FGB and FGA mRNA was approximately 2- or 4-fold higher than FGG mRNA and FGB mRNA. When FGA, FGB, or FGG mRNA expression levels were down-regulated by nearby 50%, fibrinogen concentrations in media were 78%, 49%, or 57% of the control, respectively. Conclusions Our results suggest that FGG mRNA levels limit fibrinogen expression in normal liver and HepG2 cells and that 50% reduction of FGA mRNA levels would not limit fibrinogen expression in normal liver and HepG2 cells.
机译:简介我们遇到了两名具有纯合和复合杂合FGA突变的纤维蛋白原血症患者。有趣的是,患者父母是杂合子,血浆纤维蛋白原水平正常。因此,我们假设肝脏的FGA mRNA水平高于FGB和/或FGG mRNA。材料和方法为了检验该假设,我们定量了正常肝脏和人肝细胞系HepG2细胞的mRNA水平,并进行了siRNA介导的HepG2细胞中纤维蛋白原基因的下调。使用实时定量RT-PCR测定三个正常肝脏和HepG2细胞的mRNA水平。通过添加对应于三个基因的siRNA进行HepG2细胞中FGA,FGB或FGG的下调,并测定细胞中的mRNA水平和培养基中分泌的纤维蛋白原浓度。结果正常人肝脏的mRNA水平为FGA = FGB> FGG,FGG mRNA水平比其他人低2倍,HepG2细胞的FGA> FGG> FGB,FGA mRNA约为2或4倍。高于FGG mRNA和FGB mRNA。当FGA,FGB或FGG mRNA表达水平下调约50%时,培养基中的纤维蛋白原浓度分别为对照的78%,49%或57%。结论我们的结果表明FGG mRNA水平限制了正常肝脏和HepG2细胞中纤维蛋白原的表达,FGA mRNA水平降低50%不会限制正常肝脏和HepG2细胞中纤维蛋白原的表达。

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