Huggett J F, Mustafa A, O'neal L, Mason D J
Connective Tissue Research Laboratories, School of Biosciences, Cardiff University, Museum Avenue, Wales, UK.
Biochem Soc Trans. 2002 Nov;30(Pt 6):890-3. doi: 10.1042/bst0300890.
The glutamate/aspartate transporter GLAST-1 is expressed in bone in vivo and also exists as a splice variant (GLAST-1a) in which exon 3 is excluded. Since GLAST-1 expression is regulated in bone in response to osteogenic mechanical stimuli in vivo and binding of glutamate to receptors on osteoblasts increases osteoblast number and activity in vitro, control of extracellular glutamate concentrations may be critical for balanced bone remodelling. To determine whether GLAST isoforms may act to regulate extracellular glutamate concentration in bone we investigated whether their pattern or level of expression is responsive to glutamate concentration in bone cells. GLAST-1a mRNA is expressed at lower levels than GLAST-1 mRNA in all cells examined. The GLAST-1a/GLAST-1 mRNA ratio is greater in MLO-Y4 osteocytes than in SaOS-2 osteoblast-like cells, although this does vary in SaOS-2 cells in response to extracellular glutamate concentration. Transfection of MLO-Y4 cells with green fluorescent protein (GFP)-tagged GLAST isoforms revealed a plasma membrane localization of GLAST-1, consistent with its transporter function, whereas GLAST-1a appeared to be expressed within internal vesicles. Interestingly, low extracellular glutamate concentrations redistributed GLAST-1-GFP into a similar internal expression pattern. Regulation of the expression and distribution of GLAST-1 by extracellular glutamate in bone cells indicates that it may regulate glutamate signalling in bone, consistent with its operation in the central nervous system.
谷氨酸/天冬氨酸转运体GLAST-1在体内骨组织中表达,并且还以一种剪接变体(GLAST-1a)的形式存在,其中外显子3被排除。由于GLAST-1的表达在体内骨组织中会响应成骨机械刺激而受到调节,并且谷氨酸与成骨细胞上的受体结合会增加体外成骨细胞的数量和活性,因此控制细胞外谷氨酸浓度可能对平衡的骨重塑至关重要。为了确定GLAST同工型是否可能在骨组织中调节细胞外谷氨酸浓度,我们研究了它们的表达模式或水平是否对骨细胞中的谷氨酸浓度有反应。在所有检测的细胞中,GLAST-1a mRNA的表达水平低于GLAST-1 mRNA。MLO-Y4骨细胞中的GLAST-1a/GLAST-1 mRNA比值高于SaOS-2成骨样细胞,尽管在SaOS-2细胞中该比值会因细胞外谷氨酸浓度而有所变化。用绿色荧光蛋白(GFP)标记的GLAST同工型转染MLO-Y4细胞后发现,GLAST-1定位于质膜,与其转运功能一致,而GLAST-1a似乎在内质网泡中表达。有趣的是,低细胞外谷氨酸浓度会使GLAST-1-GFP重新分布为类似的内质网表达模式。骨细胞中细胞外谷氨酸对GLAST-1表达和分布的调节表明,它可能在骨组织中调节谷氨酸信号传导,这与其在中枢神经系统中的作用一致。