Increased ambient glutamate concentration alters the expression of NMDA receptor subunits in cerebellar granule neurons

被引:24
作者
Cebers, G [1 ]
Cebere, A [1 ]
Kovács, AD [1 ]
Högberg, H [1 ]
Moreira, T [1 ]
Liljequist, S [1 ]
机构
[1] Karolinska Inst, Karolinska Hosp, Div Drug Dependence Res, Dept Clin Neurosci, SE-17176 Stockholm, Sweden
关键词
glutamate transporters; L-trans-pyrrolidine-2,4-dicarboxylate; immunocytochemistry; RT-PCR; neurotoxicity; rat;
D O I
10.1016/S0197-0186(01)00014-6
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
Effects of prolonged (48 h) inhibition of glutamate reuptake on the relative abundance of mRNAs coding for N-methyl-D-aspartate (NMDA) receptor subunits, and the expression of corresponding proteins were investigated in primary cultures of rat cerebellar granule neurons. In cells exposed to the glutamate transport blocker, L-trans-pyrrolidine-2,4-dicarboxylate (PDC), the expression of the C1 exon-positive NR1 mRNA variant was reduced by about 40% whereas, the expression of Cl-negative mRNA was increased leading to significant reduction of the +Cl/-C1 ratio. The expression of the Nl-negative NR1 variants was slightly reduced following exposure to PDC, indicating that increased medium levels of glutamate changed the relative abundance of NR1 splice-variant expression but did not reduce the overall NR1 transcription. Expression of NR2A and NR2B mRNAs was 40-50% lower in PDC-treated cells as compared to control. Immunoblot experiments revealed that PDC exposure reduced the expression of NR1 and all NR2 proteins with NR2A and NR2B proteins being reduced to a greater extent than NRL The overall decrease in NMDA receptor subunit protein expression was considerably more pronounced than the reduction of their corresponding mRNAs, suggesting involvement of a post-transcriptional regulation. Our data support the hypothesis that functional activity and number of NMDA receptors are regulated by strength of the glutamatergic input. Thus, reduced glutamate uptake resulting in increased concentration of ambient glutamate initiate a series of adaptive responses manifested as a gradual down-regulation of the functional activity and expression of NMDA receptors. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:151 / 160
页数:10
相关论文
共 58 条
[1]   CLONING AND ANALYSIS OF THE 5' FLANKING SEQUENCE OF THE RAT N-METHYL-D-ASPARTATE RECEPTOR-1 (NMDAR1) GENE [J].
BAI, G ;
KUSIAK, JW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1152 (01) :197-200
[2]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[3]   MOLECULAR-CLONING AND FUNCTIONAL EXPRESSION OF GLUTAMATE RECEPTOR SUBUNIT GENES [J].
BOULTER, J ;
HOLLMANN, M ;
OSHEAGREENFIELD, A ;
HARTLEY, M ;
DENERIS, E ;
MARON, C ;
HEINEMANN, S .
SCIENCE, 1990, 249 (4972) :1033-1037
[4]  
BULLER AL, 1994, J NEUROSCI, V14, P5471
[5]   THE CELLULAR NEUROBIOLOGY OF NEURONAL DEVELOPMENT - THE CEREBELLAR GRANULE CELL [J].
BURGOYNE, RD ;
CAMBRAYDEAKIN, MA .
BRAIN RESEARCH REVIEWS, 1988, 13 (01) :77-101
[6]   N-METHYL-D-ASPARTATE RAISES CYTOSOLIC CALCIUM-CONCENTRATION IN RAT CEREBELLAR GRANULE CELLS IN CULTURE [J].
BURGOYNE, RD ;
PEARCE, IA ;
CAMBRAYDEAKIN, M .
NEUROSCIENCE LETTERS, 1988, 91 (01) :47-52
[7]   Enhancement of NMDA-induced functional responses without concomitant NMDA receptor changes following chronic ethanol exposure in cerebellar granule cells [J].
Cebere, A ;
Cebers, G ;
Liljequist, S .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1999, 360 (06) :623-632
[8]   Prolonged inhibition of glutamate reuptake down-regulates NMDA receptor functions in cultured cerebellar granule cells [J].
Cebers, G ;
Cebere, A ;
Wägner, A ;
Liljequist, S .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (05) :2181-2190
[9]   MODULATION OF AMPA/KAINATE RECEPTORS BY CYCLOTHIAZIDE INCREASES CYTOPLASMIC FREE CA2+ AND CA-45(2+) UPTAKE IN BRAIN NEURONS [J].
CEBERS, G ;
LILJEQUIST, S .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1995, 290 (02) :105-115
[10]   EXCITOTOXIC CELL-DEATH [J].
CHOI, DW .
JOURNAL OF NEUROBIOLOGY, 1992, 23 (09) :1261-1276