Nagamatsu S, Nakamichi Y, Inoue N, Inoue M, Nishino H, Sawa H
Department of Biochemistry, Kyorin University School of Medicine, Tokyo, Japan.
Biochem J. 1996 Oct 15;319 ( Pt 2)(Pt 2):477-82. doi: 10.1042/bj3190477.
In order to establish whether growth of glioma cells is associated with glucose transport and metabolism, we investigated expression of the glucose transporter and hexokinase, as well as glucose transport and glucose phosphorylation in rat C6 glioma cells growing at different rates. Rat C6 glioma cells were subcloned to produce four different cell lines (CL1, CL2, CL3 and CL4) differing in growth, differentiation and morphology: CL1 cells were slow-growing with an astrocytic appearance whereas CL4 cells grew rapidly and were small and spindle-shaped. Immunocytochemical analysis using glial fibrillary acidic protein and galactocerebroside antibodies revealed that CL1 and CL4 cells differentiate to astrocytes and oligodendrocytes respectively. Both of these cell lines expressed GLUT1 mRNA predominantly, whereas little GLUT3 mRNA was evident by Northern-blot analysis. The GLUT1 mRNA level was much higher in CL4 than in CL1 cells, and the uptake of 2-deoxy-D-glucose and 3-O-methyl-D-glucose by CL4 cells was markedly higher than that by CL1 cells, indicating a correlation between the growth rate, glucose transporter (GLUT1) level and glucose-transport rate of C6 glioma cells. We then studied glucose metabolism by CL1 and CL4 cells by measuring their hexokinase activities and intracellular concentrations of glucose and ATP. The mitochondrial hexokinase activity of CL4 cells was about three times higher than that of CL1 cells, whereas the cytosolic hexokinase activity of CL4 cells was only about half that of CL1 cells. As the total amount of cellular hexokinase protein in CL4 cells was only slightly higher (about 20%) than that in CL1 cells, the hexokinase protein of CL4 cells was considered to have moved from the cytosol to the mitochondrial membranes. Consistent with the increased mitochondrial hexokinase activity of CL4 cells, the intracellular glucose concentration was undetectable, and the ATP concentration was higher than that of CL1 cells, suggesting that glucose transport is the rate-limiting factor for overall glucose metabolism is rapidly growing C6 cells. Therefore the present data demonstrate that glioma cell growth is related to glucose transport, which is closely associated with glucose metabolism.
为了确定胶质瘤细胞的生长是否与葡萄糖转运和代谢相关,我们研究了葡萄糖转运蛋白和己糖激酶的表达,以及不同生长速率的大鼠C6胶质瘤细胞中的葡萄糖转运和葡萄糖磷酸化情况。将大鼠C6胶质瘤细胞亚克隆以产生四种生长、分化和形态不同的细胞系(CL1、CL2、CL3和CL4):CL1细胞生长缓慢,呈星形胶质细胞外观,而CL4细胞生长迅速,体积小且呈纺锤形。使用胶质纤维酸性蛋白和半乳糖脑苷脂抗体进行免疫细胞化学分析表明,CL1和CL4细胞分别分化为星形胶质细胞和少突胶质细胞。这两种细胞系均主要表达GLUT1 mRNA,而通过Northern印迹分析几乎未检测到GLUT3 mRNA。CL4细胞中的GLUT1 mRNA水平远高于CL1细胞,并且CL4细胞对2-脱氧-D-葡萄糖和3-O-甲基-D-葡萄糖的摄取明显高于CL1细胞,表明C6胶质瘤细胞的生长速率、葡萄糖转运蛋白(GLUT1)水平和葡萄糖转运速率之间存在相关性。然后,我们通过测量CL1和CL4细胞的己糖激酶活性以及细胞内葡萄糖和ATP的浓度来研究它们的葡萄糖代谢。CL4细胞的线粒体己糖激酶活性约为CL1细胞的三倍,而CL4细胞的胞质己糖激酶活性仅约为CL1细胞的一半。由于CL4细胞中细胞己糖激酶蛋白的总量仅比CL1细胞略高(约20%),因此认为CL4细胞的己糖激酶蛋白已从胞质溶胶转移至线粒体膜。与CL4细胞中线粒体己糖激酶活性增加一致,细胞内葡萄糖浓度无法检测到,并且ATP浓度高于CL1细胞,这表明葡萄糖转运是快速生长的C6细胞整体葡萄糖代谢的限速因素。因此,目前的数据表明胶质瘤细胞的生长与葡萄糖转运相关,而葡萄糖转运与葡萄糖代谢密切相关。