Correlating physiology with gene expression in striatal cholinergic neurones

被引:49
作者
Richardson, PJ
Dixon, AK
Lee, K
Bell, MI
Cox, PJ
Williams, R
Pinnock, RD
Freeman, TC
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
[2] Sanger Ctr, Cambridge, England
[3] Parke Davis Neurosci Res Ctr, Cambridge, England
关键词
gene expression; functional activity correlation; rat; cholinergic neurones; striatum; transmitters;
D O I
10.1046/j.1471-4159.2000.740839.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The expression of 34 transmitter-related genes has been examined in the cholinergic neurones of rat striatal brain slices, with the aim of correlating gene expression with functional activity. The mRNAs encoding types I, II/IIA, and III alpha subunits of the voltage-sensitive sodium channels were detected, suggesting the presence of these three types of sodium channel. Similarly, mRNAs: encoding all four alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate (AMPA)-type glutamate receptor subunits and the NR1 and NR2A, 2B, and 2D subunits of the NMDA-type glutamate receptors were detected, suggesting that various combinations of these subunits mediate the cellular response to synaptically released glutamate. Other mRNAs detected included the NK1 and NK3 tachykinin receptors, all four known adenosine receptors, and the GABA-synthesising enzyme glutamate decarboxylase, Subpopulations of these cholinergic neurones have been identified on the basis of the expression of the NK3 tachykinin receptor in 5% and the trkC neurotrophin receptor in 12% of the cells investigated.
引用
收藏
页码:839 / 846
页数:8
相关论文
共 35 条
[1]
Angulo MC, 1997, J NEUROSCI, V17, P6685
[2]
[Anonymous], TRENDS NEUROSCI
[3]
Bell M. I., 1998, Society for Neuroscience Abstracts, V24, P802
[4]
Characterization of the mechanism of action of tachykinins in rat striatal cholinergic interneurons [J].
Bell, MI ;
Richardson, PJ ;
Lee, K .
NEUROSCIENCE, 1998, 87 (03) :649-658
[5]
Bernard V, 1997, J NEUROSCI, V17, P819
[6]
Spinal sensory neurons express multiple sodium channel alpha-subunit mRNAs [J].
Black, JA ;
DibHajj, S ;
McNabola, K ;
Jeste, S ;
Rizzo, MA ;
Kocsis, JD ;
Waxman, SG .
MOLECULAR BRAIN RESEARCH, 1996, 43 (1-2) :117-131
[7]
SUBUNIT COMPOSITION AT THE SINGLE-CELL LEVEL EXPLAINS FUNCTIONAL-PROPERTIES OF A GLUTAMATE-GATED CHANNEL [J].
BOCHET, P ;
AUDINAT, E ;
LAMBOLEZ, B ;
CREPEL, F ;
ROSSIER, J ;
IINO, M ;
TSUZUKI, K ;
OZAWA, S .
NEURON, 1994, 12 (02) :383-388
[8]
Options available - from start to finish - for obtaining expression data by microarray [J].
Bowtell, DDL .
NATURE GENETICS, 1999, 21 (Suppl 1) :25-32
[9]
COMPLETE SEQUENCE OF A CDNA-ENCODING AN ACTIVE-RAT CHOLINE-ACETYLTRANSFERASE - A TOOL TO INVESTIGATE THE PLASTICITY OF CHOLINERGIC PHENOTYPE EXPRESSION [J].
BRICE, A ;
BERRARD, S ;
RAYNAUD, B ;
ANSIEAU, S ;
COPPOLA, T ;
WEBER, MJ ;
MALLET, J .
JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 23 (03) :266-273
[10]
BOTH A1 AND A2A PURINE RECEPTORS REGULATE STRIATAL ACETYLCHOLINE-RELEASE [J].
BROWN, SJ ;
JAMES, S ;
REDDINGTON, M ;
RICHARDSON, PJ .
JOURNAL OF NEUROCHEMISTRY, 1990, 55 (01) :31-38