Chua B H, Chua C C, Zhao Z Y, Krebs C J
Department of Pathology, Wayne State University, School of Medicine, Detroit, MI 48202.
J Recept Res. 1991;11(6):941-57. doi: 10.3109/10799899109064689.
The genetically diabetic db/db mouse is an excellent model to study the effect of diabetes on hormone receptors. The decrease of EGF binding sites could be detected in the hepatic microsomes of diabetic mice as early as 3 weeks of age. In addition, there was an age-related decrease in the autophosphorylating activity of EGF receptor isolated from the liver of diabetic mice. Estrone feeding (0.005%) partially restored this autophosphorylating activity. Northern blot analysis showed that the hepatic EGF receptor transcripts were dramatically decreased during the progression of diabetes and could be reversed by estrone feeding. Transfection experiments carried out on HepG2 cells using EGF receptor promoter (pERCAT-6) demonstrated that addition of 2 x 10(-8) M estrone stimulated chloramphenicol acetyltransferase activity. Our results suggest that estrone modulates EGF receptor by enhancing EGF receptor transcripts and the promoter activity of this gene.
遗传性糖尿病db/db小鼠是研究糖尿病对激素受体影响的优良模型。早在3周龄时,就能在糖尿病小鼠的肝微粒体中检测到表皮生长因子(EGF)结合位点的减少。此外,从糖尿病小鼠肝脏分离出的EGF受体的自身磷酸化活性也存在与年龄相关的降低。给予雌酮(0.005%)可部分恢复这种自身磷酸化活性。Northern印迹分析表明,在糖尿病进展过程中,肝脏中的EGF受体转录本显著减少,而给予雌酮可使其逆转。使用EGF受体启动子(pERCAT-6)对HepG2细胞进行的转染实验表明,添加2×10⁻⁸ M的雌酮可刺激氯霉素乙酰转移酶活性。我们的结果表明,雌酮通过增强EGF受体转录本和该基因的启动子活性来调节EGF受体。