Luyt Karen, Varadi Aniko, Molnar Elek
MRC Centre for Synaptic Plasticity, Department of Anatomy, University of Bristol, Bristol, UK.
J Neurochem. 2003 Mar;84(6):1452-64. doi: 10.1046/j.1471-4159.2003.01661.x.
We investigated the expression of metabotropic glutamate receptor (mGluR) isoforms in CG-4 rodent oligodendroglial progenitor cells (OPC) and rat brain oligodendrocytes. Our RT-PCR analysis detected mRNAs for mGluR3 and mGluR5 isoforms in OPCs. Although neurons express both mGluR5a and mGluR5b splice variants, only mGluR5a was identified in OPCs. Antibodies to mGluR2/3 and mGluR5 detected the corresponding receptor proteins in immunoblots of OPC membrane fractions. Furthermore, immunocytochemical analysis identified mGluR5 in oligodendrocyte marker O4-positive OPCs. The expression of mGluR5 was also demonstrated in oligodendrocyte marker (O4 and O1) positive cells in white matter of postnatal 4- and 7-day-old rat brain sections using immunofluorescent double labelling and confocal microscopy. The mGluR5 receptor function was assessed in CG-4 OPCs with fura-2 microfluorometry. Application of the mGluR1/5 specific agonist (S)-3,5-dihydroxyphenylglycine (DHPG) induced calcium oscillations, which were inhibited by the selective mGluR5 antagonist 2-methyl-6-(phenylethynyl) pyridine hydrochloride (MPEP). The DHPG induced calcium oscillations required Ca2+ release from intracellular stores. In OPCs the group II mGluR agonist (2S,2'R,3'R)-2-(2',3'-dicarboxycyclopropyl)glycine (DCG-IV) decreased forskolin-stimulated cAMP synthesis, indicating the presence of functional mGluR3. The newly identified mGluR3 and mGluR5a may be involved in the differentiation of oligodendrocytes, myelination and the development of white matter damage.
我们研究了代谢型谷氨酸受体(mGluR)亚型在CG-4啮齿动物少突胶质前体细胞(OPC)和大鼠脑少突胶质细胞中的表达。我们的逆转录聚合酶链反应(RT-PCR)分析在OPC中检测到了mGluR3和mGluR5亚型的信使核糖核酸(mRNA)。虽然神经元同时表达mGluR5a和mGluR5b剪接变体,但在OPC中仅鉴定出mGluR5a。针对mGluR2/3和mGluR5的抗体在OPC膜组分的免疫印迹中检测到了相应的受体蛋白。此外,免疫细胞化学分析在少突胶质细胞标志物O4阳性的OPC中鉴定出了mGluR5。使用免疫荧光双重标记和共聚焦显微镜,在出生后4天和7天的大鼠脑切片白质中少突胶质细胞标志物(O4和O1)阳性细胞中也证实了mGluR5的表达。用fura-2显微荧光测定法在CG-4 OPC中评估了mGluR5受体功能。代谢型谷氨酸受体1/5特异性激动剂(S)-3,5-二羟基苯甘氨酸(DHPG)的应用诱导了钙振荡,这被选择性mGluR5拮抗剂盐酸2-甲基-6-(苯乙炔基)吡啶(MPEP)所抑制。DHPG诱导的钙振荡需要从细胞内储存中释放钙离子。在OPC中,II组代谢型谷氨酸受体激动剂(2S,2'R,3'R)-2-(2',3'-二羧基环丙基)甘氨酸(DCG-IV)降低了福斯高林刺激的环磷酸腺苷(cAMP)合成,表明存在功能性mGluR3。新鉴定出的mGluR3和mGluR5a可能参与少突胶质细胞的分化、髓鞘形成以及白质损伤的发展。