Bristol L A, Rothstein J D
Department of Neurology, Johns Hopkins University, Baltimore, MD 21287, USA.
Ann Neurol. 1996 May;39(5):676-9. doi: 10.1002/ana.410390519.
Glutamate transport is critical for synaptic inactivation of glutamate and prevention of excitotoxicity. The following four glutamate transporters have been identified in human brain: EAAT1, EAAT2, EAAT3, and EAAT4. Deficient glutamate transport has been identified in the motor cortex and the spinal cord of tissue from amyotrophic lateral sclerosis (ALS) patients. The defect appears to be due to a selective loss of the astroglial specific glutamate transporter protein EAAT2. In these studies we sought to extend our understanding of glutamate transporters in ALS by examining the mRNA for each transporter subtype in ALS motor cortex. All tissue was matched for age and postmortem delay. There was no quantitative change in mRNA for EAAT1, EAAT2, or EAAT3 in ALS motor cortex, even in patients with a large loss of EAAT2 protein (95% decrease compared with control) and decreased tissue glutamate transport (73% decrease compared with control). These studies suggest that the dramatic abnormalities in EAAT2 may be due to translational or post-translational processes.
谷氨酸转运对于谷氨酸的突触失活和预防兴奋性毒性至关重要。在人类大脑中已鉴定出以下四种谷氨酸转运体:EAAT1、EAAT2、EAAT3和EAAT4。在肌萎缩侧索硬化症(ALS)患者的运动皮层和脊髓组织中已发现谷氨酸转运不足。这种缺陷似乎是由于星形胶质细胞特异性谷氨酸转运体蛋白EAAT2的选择性缺失所致。在这些研究中,我们试图通过检测ALS运动皮层中每种转运体亚型的mRNA来扩展我们对ALS中谷氨酸转运体的理解。所有组织均根据年龄和死后延迟进行匹配。在ALS运动皮层中,EAAT1、EAAT2或EAAT3的mRNA没有定量变化,即使在EAAT2蛋白大量缺失(与对照组相比减少95%)且组织谷氨酸转运减少(与对照组相比减少73%)的患者中也是如此。这些研究表明,EAAT2中的显著异常可能是由于翻译或翻译后过程所致。