Expression of glutamate transporters and ionotropic glutamate receptors in GLAST knockout mice

被引:26
作者
Ueda, Y
Doi, T
Tsuru, N
Tokumaru, J
Mitsuyama, Y
机构
[1] Miyazaki Med Coll, Dept Psychiat, Miyazaki 8891692, Japan
[2] Miyazaki Med Coll, Dept Psychol, Miyazaki 8891692, Japan
来源
MOLECULAR BRAIN RESEARCH | 2002年 / 104卷 / 02期
关键词
glutamate receptor; knockout; seizure; hippocampus; cortex; mice;
D O I
10.1016/S0169-328X(02)00325-X
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
In order to investigate the molecular mechanism underlying high seizure susceptibility of GLAST knockout mice, we carried out Western blotting for the expression of GLT-1, EAAC-1, and several kinds of glutamate receptors in the hippocampus and the cortex. Although no significant difference was observed between GLAST (+/+) and (-/-) mice in terms of expression of GLT-1 and EAAC-1 in the hippocampus, these proteins were over-expressed in the frontal cortex in GLAST (-/-) mice (GLT-1, about 210% increase; EAAC-1, about 180% increase). Expression of hippocampal Glu-R1 and Glu-R2 in GLAST (-/-) mice was remarkably increased (Glu-R1, about 140% increase; Glu-R2, about 160% increase), while Glu-R3 and NMDA receptors levels (NMDA-RI, 2A and 2B) were equal to those in control. Cortical levels of Glu-R1, -R2 and -R3 receptors in GLAST (-/-) mice were remarkably decreased (Glu-R1, about 60% decrease; Glu-R2, about 60% decrease; Glu-R3, about 70% decrease), while NMDA receptors were remarkably increased in comparison to those in GLAST (+/+) mice (N-R1, about 150% increase; N-R2A, about 150% increase;, N-R2B, about 140% increase). These data suggest that the increased susceptibility to seizures in GLAST (-/-) mice might be derived from increased expression of Glu-R1 in the hippocampus coupled with decreased cortical expression of Glu-R2 and increased NMDA-R1 and -2A, -2B expression. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:120 / 126
页数:7
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