Nagamatsu S, Sawa H, Inoue N, Nakamichi Y, Takeshima H, Hoshino T
Department of Biochemistry, Kyorin University School of Medicine, Tokyo, Japan.
Biochem J. 1994 May 15;300 ( Pt 1)(Pt 1):125-31. doi: 10.1042/bj3000125.
This study was designed to determine whether glucose regulates the gene expression of glucose transporter GLUT3 in neurons. We examined the regulation of GLUT3 mRNA by glucose in vivo in mouse brain and in vitro by using neuronal cultures from rat embryos. Hypoglycaemia (< 30 mg/dl), produced by 72 h of starvation, increased GLUT3 mRNA in mouse brain by 2-fold. Hybridization studies in situ demonstrated that hypoglycaemia-induced increases in GLUT3 mRNA expression were observed selectively in brain regions including the hippocampus, dentate gyrus, cerebral cortex and piriform cortex, but not the cerebellum. Primary neuronal cultures from rat embryos deprived of glucose for 48 h also showed an increase (4-fold over control) in GLUT3 mRNA, indicating that glucose can directly regulate expression of GLUT3 mRNA. In contrast with hypoglycaemia, hyperglycaemia produced by streptozotocin did not alter the expression of GLUT3 mRNA. We also confirmed previous findings that hypoglycaemia increases GLUT1 mRNA expression in brain. The increase in GLUT1 expression was probably limited to the blood-brain barrier in vivo, since GLUT1 mRNA could not be detected in neurons of the mouse cerebrum. Thus we conclude that up-regulation of neuronal GLUT3 in response to glucose starvation represents a protective mechanism against energy depletion in neurons.
本研究旨在确定葡萄糖是否调节神经元中葡萄糖转运蛋白GLUT3的基因表达。我们通过在小鼠脑中进行体内实验以及利用大鼠胚胎神经元培养物进行体外实验,研究了葡萄糖对GLUT3 mRNA的调节作用。饥饿72小时导致低血糖(<30mg/dl),使小鼠脑中的GLUT3 mRNA增加了2倍。原位杂交研究表明,低血糖诱导的GLUT3 mRNA表达增加选择性地出现在包括海马体、齿状回、大脑皮层和梨状皮层在内的脑区,但小脑未出现。来自大鼠胚胎的原代神经元培养物在无糖培养48小时后,GLUT3 mRNA也出现增加(比对照增加4倍),表明葡萄糖可直接调节GLUT3 mRNA的表达。与低血糖相反,链脲佐菌素诱导的高血糖并未改变GLUT3 mRNA的表达。我们还证实了先前的研究结果,即低血糖会增加脑中GLUT1 mRNA的表达。GLUT1表达的增加在体内可能仅限于血脑屏障,因为在小鼠大脑的神经元中未检测到GLUT1 mRNA。因此,我们得出结论,神经元对葡萄糖饥饿的反应中GLUT3的上调代表了一种针对神经元能量耗竭的保护机制。