Parini P, Angelin B, Lobie P E, Norstedt G, Rudling M
Department of Medicine, Karolinska Institute, Huddinge University Hospital, Sweden.
Endocrinology. 1995 Sep;136(9):3767-73. doi: 10.1210/endo.136.9.7649083.
Human GH (hGH) has been shown to stimulate hepatic low density lipoprotein (LDL) receptor expression in man in vivo. To further characterize this effect in vitro, we determined the expression of LDL receptors in cultured human hepatoma (HepG2) cells exposed to hGH. After incubation with hGH, stimulation of LDL receptors appeared at a concentration of 0.25 nM hGH. The presence of hGH receptors on HepG2 cells could be demonstrated by immunocytochemistry using a hGH receptor-specific monoclonal antibody. Binding studies, using 125I-labeled hGH, revealed high affinity binding with the appropriate somatogenic specificity. The LDL receptor induction was specific for hGH, as both bovine GH and recombinant human PRL were without effect. The LDL receptor stimulation occurred in parallel with increased levels of LDL receptor messenger RNA. Inclusion of dexamethasone and thyroid hormone in the incubation medium enhanced the LDL receptor stimulation by hGH. Although incubation with insulin-like growth factor-I (IGF-I) stimulated LDL receptor expression, the hGH-induced stimulation was unaltered after preincubation of cells with a monoclonal mouse anti-IGF-I antibody, suggesting that the release of IGF-I is not involved in LDL receptor stimulation by hGH. We conclude that hGH specifically induces the LDL receptor in cultured HepG2 cells at both the protein and the messenger RNA level, and that the induction is independent of IGF-I release.
已证实在人体内,人生长激素(hGH)可刺激肝脏低密度脂蛋白(LDL)受体的表达。为在体外进一步明确这种作用,我们测定了暴露于hGH的培养人肝癌(HepG2)细胞中LDL受体的表达。用hGH孵育后,在0.25 nM hGH浓度时出现LDL受体的刺激作用。使用hGH受体特异性单克隆抗体通过免疫细胞化学可证实HepG2细胞上存在hGH受体。利用125I标记的hGH进行的结合研究显示出具有适当促生长特异性的高亲和力结合。LDL受体诱导对hGH具有特异性,因为牛生长激素和重组人催乳素均无作用。LDL受体刺激与LDL受体信使核糖核酸水平升高同时发生。在孵育培养基中加入地塞米松和甲状腺激素可增强hGH对LDL受体的刺激作用。虽然用胰岛素样生长因子-I(IGF-I)孵育可刺激LDL受体表达,但在用小鼠抗IGF-I单克隆抗体对细胞进行预孵育后,hGH诱导的刺激作用未改变,这表明IGF-I的释放不参与hGH对LDL受体的刺激作用。我们得出结论,hGH在蛋白质和信使核糖核酸水平上均能特异性诱导培养的HepG2细胞中的LDL受体,且这种诱导作用与IGF-I的释放无关。