Gebhardt R, Schuler M, Schörner D
Physiologisch-chemisches, Institut der Universität, Tübingen, Germany.
Biochem Biophys Res Commun. 1998 May 29;246(3):895-8. doi: 10.1006/bbrc.1998.8720.
Cocultivation of primary pig hepatocytes with RL-ET-14 cells, an endothelial-like cell line resulted in spontaneous induction of glutamine synthetase (GS)-activity in the hepatocytes by more than 10-fold within 120 h to 144 h. Hepatocyte-specific induction was confirmed by immunocytochemistry. Addition of trijodothyronine (T3) to the culture medium inhibited the induction in a concentration dependent manner. No comparable influence of T3 was seen with pure cultures of either cell type suggesting that only the spontaneous induction was affected. Other hormones such as glucagon, insulin, growth hormone, epinephrine and testosterone did not interfere with the induction. Addition of several protein kinase-inhibitors such as staurosporine and genistein were without influence. However, a strong inhibition was found after addition of okadaic acid in nanomolar concentrations indicating an involvement of protein-phosphatase 2A in the induction process.
原代猪肝细胞与RL - ET - 14细胞(一种内皮样细胞系)共培养,导致肝细胞中的谷氨酰胺合成酶(GS)活性在120小时至144小时内自发诱导增加超过10倍。免疫细胞化学证实了肝细胞特异性诱导。向培养基中添加三碘甲状腺原氨酸(T3)以浓度依赖的方式抑制了这种诱导。在两种细胞类型的纯培养物中未观察到T3的类似影响,这表明只有自发诱导受到影响。其他激素如胰高血糖素、胰岛素、生长激素、肾上腺素和睾酮不干扰这种诱导。添加几种蛋白激酶抑制剂如星形孢菌素和染料木黄酮没有影响。然而,添加纳摩尔浓度的冈田酸后发现有强烈抑制作用,表明蛋白磷酸酶2A参与了诱导过程。