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Insulin secretion, insulin content and glucose phosphorylation in RINm5F insulinoma cells after transfection with human GLUT2 glucose-transporter cDNA

机译:人GLUT2葡萄糖转运蛋白cDNA转染后的RINm5F胰岛素瘤细胞中的胰岛素分泌,胰岛素含量和葡萄糖磷酸化

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pThe insulin-secretory response to glucose is defective in the RINm5F insulin-producing tumour cell line. Stable transfection with human low-affinity GLUT2 glucose-transporter cDNA revealed a significant improvement in stimulus-secretion coupling in these insulinoma cells. 3-O-Methylglucose uptake increased 10-fold in the concentration range 10-20 mM, whereas non-transfected control cells were unresponsive. Northern-blot analysis revealed a 7-fold increase in expression of the insulin gene in the GLUT2-transfected RINm5F cell clone T1. In contrast, glucokinase and GLUT1 glucose-transporter mRNA gene expression were not affected by transfection with GLUT2 glucose-transporter cDNA. The insulin content of transfected RINm5F cells was 7-fold higher after tissue culture at high glucose concentrations than in non-transfected controls. GLUT2-transfected RINm5F cells also regained insulin-secretory responsiveness toward high glucose concentrations. Tissue culture for 72 h in 20 mM glucose induced glucokinase activity in the GLUT2-transfected RINm5F clone T1, raising the glucokinase/hexokinase phosphorylation ratio from 0.2 to 0.6. The experiments demonstrate that an increased glucose uptake via a low-affinity glucose transporter and an increased metabolic flux rate are important factors in the induction of insulin-gene expression and glucokinase activity and thus improved glucose-induced biosynthesis and secretion of insulin in RINm5F insulinoma cells./p
机译:>在产生RINm5F的胰岛素的肿瘤细胞系中对葡萄糖的胰岛素分泌反应有缺陷。人低亲和力GLUT2葡萄糖转运蛋白cDNA的稳定转染显示出这些胰岛素瘤细胞中刺激-分泌偶联的显着改善。在10-20 mM的浓度范围内,3-O-甲基葡萄糖的摄取增加了10倍,而未转染的对照细胞则无反应。 Northern印迹分析表明,在GLUT2转染的RINm5F细胞克隆T1中,胰岛素基因的表达增加了7倍。相反,葡萄糖激酶和GLUT1葡萄糖转运蛋白mRNA基因表达不受GLUT2葡萄糖转运蛋白cDNA转染的影响。组织培养后在高葡萄糖浓度下转染的RINm5F细胞的胰岛素含量比未转染的对照组高7倍。 GLUT2转染的RINm5F细胞还恢复了对高葡萄糖浓度的胰岛素分泌反应。在GLUT2转染的RINm5F克隆T1中,在20 mM葡萄糖中进行的组织培养72小时诱导了葡萄糖激酶活性,使葡萄糖激酶/己糖激酶的磷酸化率从0.2提高到0.6。实验表明,通过低亲和力葡萄糖转运蛋白增加的葡萄糖摄取和增加的代谢通量速率是诱导胰岛素基因表达和葡萄糖激酶活性从而改善RINm5F胰岛素瘤细胞中葡萄糖诱导的生物合成和胰岛素分泌的重要因素。

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