Lu D, Hoshino H, Takeuchi T
Department of Molecular Medicine, Institute for Molecular and Cellular Regulation, Gunma University, Japan.
FEBS Lett. 1996 Dec 9;399(1-2):37-42. doi: 10.1016/s0014-5793(96)01275-6.
We engineered a hepatoma cell line that produces an up-regulation of insulin in response to cAMP, dexamethasone, and retinoic acid, and a down-regulation in response to insulin. We devised a regulatory secretion system by placing proinsulin DNA under the regulatable promoter for phosphoenolpyruvate carboxykinase (PEPCK). To assess the ability to regulate insulin secretion, we used the rat hepatoma cell line, H4IIE. The H4IIE cells secreted immunoreactive insulin (IRI) constantly at a level of 1-3 fmol/10(6) cells/h. IRI increased approximately two-fold upon stimulation with 0.5 mM cAMP and five-fold with the addition of the cAMP-dependent phosphodiesterase inhibitor IBMX, as compared to baseline IRI secretion. IRI increased 18-fold by 1-500 nM dexamethasone together with cAMP and IBMX. Addition of exogenous insulin to the culture medium significantly decreased insulin mRNA expression on Northern blot.
我们构建了一种肝癌细胞系,该细胞系在受到环磷酸腺苷(cAMP)、地塞米松和视黄酸刺激时会产生胰岛素上调,而在受到胰岛素刺激时会产生下调。我们通过将胰岛素原DNA置于磷酸烯醇式丙酮酸羧激酶(PEPCK)的可调节启动子下,设计了一种调节分泌系统。为了评估调节胰岛素分泌的能力,我们使用了大鼠肝癌细胞系H4IIE。H4IIE细胞以1 - 3 fmol/10⁶细胞/小时的水平持续分泌免疫反应性胰岛素(IRI)。与基线IRI分泌相比,用0.5 mM cAMP刺激后IRI增加约两倍,添加cAMP依赖性磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)后增加五倍。与cAMP和IBMX一起,1 - 500 nM地塞米松使IRI增加18倍。向培养基中添加外源性胰岛素在Northern印迹上显著降低了胰岛素mRNA表达。