Lescoat G, Loreal O, Moirand R, Dezier J F, Pasdeloup N, Deugnier Y, Brissot P
Unité de Recherches Hépatologiques, INSERM U 49, CHRU Pontchaillou, Rennes, France.
Liver. 1989 Jun;9(3):179-85. doi: 10.1111/j.1600-0676.1989.tb00396.x.
In order to determine if iron was able to stimulate specifically ferritin synthesis and secretion in transformed human hepatocytes in culture, human hepatoma cell (HepG2) cultures were submitted to increasing doses of ferric nitrilotriacetate. Iron uptake by the cells was demonstrated by incorporation of 59 Fe and the staining method of Perls. The following results were obtained: 1. iron incorporation within the hepatocytes increased as a function of culture time; 2. during the first 24 h of treatment, ferritin synthesis increased progressively, in parallel to the iron uptake; 3. a dose-dependent significant stimulation of ferritin synthesis and secretion were observed when the medium iron concentration increased from 5 to 20 mumol/l; 4. albumin, transthyretin and transferrin secretions were unaffected. These data demonstrated that, in our hepatocyte culture model, iron load increased the expression of ferritin in a highly specific manner.
为了确定铁是否能够特异性地刺激培养的转化人肝细胞中铁蛋白的合成与分泌,将人肝癌细胞(HepG2)培养物用递增剂量的次氮基三乙酸铁处理。通过掺入59Fe和Perls染色法证实细胞对铁的摄取。获得了以下结果:1. 肝细胞内的铁掺入量随培养时间增加;2. 在处理的前24小时内,铁蛋白合成逐渐增加,与铁摄取平行;3. 当培养基中铁浓度从5微摩尔/升增加到20微摩尔/升时,观察到铁蛋白合成和分泌有剂量依赖性的显著刺激;4. 白蛋白、转甲状腺素蛋白和转铁蛋白的分泌未受影响。这些数据表明,在我们的肝细胞培养模型中,铁负荷以高度特异性的方式增加了铁蛋白的表达。