Fladeby C, Bjønness B, Serck-Hanssen G
Department of Physiology, University of Bergen, Norway.
J Cell Physiol. 1996 Nov;169(2):242-7. doi: 10.1002/(SICI)1097-4652(199611)169:2<242::AID-JCP3>3.0.CO;2-O.
Regulation of glucose transport was studied in primary cultures of bovine chromaffin cells (BCC) using the glucose analogue 2-deoxyglucose (DOG) as a model substrate. The glucose transporter in freshly isolated and cultured BCC was identified as GLUT1 by Western immunoblots. The level of GLUT1 increased by time in culture and was followed by an enhancement in uptake of DOG. The DOG uptake was stimulated by insulin-like growth factor I (IGF-I) with an EC50 of 1 nM and a maximal response (approximately 2-fold) was obtained at 10-100 nM IGF-I. Insulin was at least 100-fold less potent than IGF-I. Exposure to 10(-8) M IGF-I also caused a redistribution of GLUT1 from an intracellular compartment to a plasma membrane-enriched fraction. Our results demonstrate a GLUT1-mediated glucose uptake in adrenomedullary cells. An enhanced glucose transport in response to IGF-I appears to be coupled to activation of IGF receptor type 1 and GLUT1 translocation.
利用葡萄糖类似物2-脱氧葡萄糖(DOG)作为模型底物,对牛嗜铬细胞(BCC)原代培养物中的葡萄糖转运调节进行了研究。通过蛋白质免疫印迹法将新鲜分离和培养的BCC中的葡萄糖转运蛋白鉴定为GLUT1。GLUT1的水平随培养时间增加,随后DOG摄取增强。胰岛素样生长因子I(IGF-I)刺激DOG摄取,其半数有效浓度(EC50)为1 nM,在10 - 100 nM IGF-I时获得最大反应(约2倍)。胰岛素的效力比IGF-I至少低100倍。暴露于10(-8) M IGF-I也会导致GLUT1从细胞内区室重新分布到富含质膜的部分。我们的结果表明肾上腺髓质细胞中存在GLUT1介导的葡萄糖摄取。对IGF-I的葡萄糖转运增强似乎与1型IGF受体的激活和GLUT1易位有关。