Glutamine synthetase down-regulation reduces astrocyte protection against glutamate excitotoxicity to neurons

被引:161
作者
Zou, Jian [2 ]
Wang, Yan-Xia [2 ]
Dou, Fang-Fang [2 ]
Lue, He-Zuo [2 ]
Ma, Zheng-Wen [2 ]
Lu, Pei-Hua [2 ]
Xu, Xiao-Ming [1 ,2 ,3 ,4 ]
机构
[1] Indiana Univ Sch Med, Stark Neurosci Res Inst, Spinal Cord & Brain Injury Res Grp, Indianapolis, IN 46202 USA
[2] Shanghai Jiao Tong Univ, Dept Neurobiol, Sch Med, Shanghai 200025, Peoples R China
[3] Indiana Univ Sch Med, Dept Neurol Surg, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
关键词
Glutamate; Glutamate uptake; Glutamine; Glutamine synthetase; TNF-alpha; Astrocyte; Neuroexcitotoxicity; TUMOR-NECROSIS-FACTOR; SPINAL-CORD-INJURY; NF-KAPPA-B; FACTOR-ALPHA; GLIAL-CELLS; MULTIPLE-SCLEROSIS; NEURAL RETINA; ADULT RATS; EXPRESSION; MOUSE;
D O I
10.1016/j.neuint.2009.12.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although the role of astrocyte glutamate transporters in glutamate clearance is well illustrated, the role of glutamine synthetase (GS) that influences this process remains to be elucidated. We examined whether GS affected the uptake of glutamate in astrocytes in vitro. The glutamate uptake was assessed by measuring the concentration of glutamate and glutamine in culture medium in the presence or absence of glutamate. We demonstrated that inhibition of GS in astrocytes by MSO significantly impaired glutamate uptake and glutamine release. Conversely, induction of GS expression in astrocytes by gene transfer significantly enhanced the glutamate uptake and glutamine release. When an inflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) was applied to the cultures, it significantly reduced GS expression and inhibited glutamate-induced GS activation resulting in increased excitotoxicity to neurons. These results suggest that GS in astrocytes may represent a novel target for neuroprotection against neuronal dysfunction and death that occur in many neurological disorders. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:577 / 584
页数:8
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