MOLECULAR-CLONING OF THE RAT ADENOSINE-A2 RECEPTOR - SELECTIVE COEXPRESSION WITH D2-DOPAMINE RECEPTORS IN RAT STRIATUM

被引:590
作者
FINK, JS
WEAVER, DR
RIVKEES, SA
PETERFREUND, RA
POLLACK, AE
ADLER, EM
REPPERT, SM
机构
[1] HARVARD UNIV, MASSACHUSETTS GEN HOSP, SCH MED, MOLEC NEUROBIOL LAB, BOSTON, MA 02114 USA
[2] HARVARD UNIV, MASSACHUSETTS GEN HOSP, SCH MED, DEV CHRONOBIOL LAB, BOSTON, MA 02114 USA
[3] HARVARD UNIV, SCH MED, DEPT NEUROL, BOSTON, MA 02114 USA
[4] HARVARD UNIV, SCH MED, DEPT PEDIAT & ANESTHESIA, BOSTON, MA 02114 USA
来源
MOLECULAR BRAIN RESEARCH | 1992年 / 14卷 / 03期
关键词
ADENOSINE; ADENOSINE A2-RECEPTOR; BASAL GANGLIA; DOPAMINE; DOPAMINE D2-RECEPTOR; CDNA;
D O I
10.1016/0169-328X(92)90173-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A cDNA fragment homologous to other G protein-coupled receptors was isolated from rat brain using the PCR method and demonstrated to be abundantly expressed in striatum. Using this fragment as a probe, a 2.1 kb full-length cDNA was isolated from a rat striatal cDNA library. This cDNA encodes a protein of 410 amino acids and is highly homologous to previously isolated adenosine receptor cDNAs. Expression of this cDNA in COS cells revealed high affinity (K(d) = 38.6 nM) and saturable binding of the A2 adenosine receptor-selective ligand [H-3]CGS 21680. Agonist displacement profile of [H-3]CGS 21680 binding was consistent with an adenosine receptor of the A2 subtype (NECA > (R)-PIA > CPA > (S)-PIA). In situ hybridization demonstrated that rat A2 adenosine receptor mRNA was co-expressed in the same striatal neurons as D2 dopamine receptor mRNA, and never co-expressed with striatal D1 dopamine receptor mRNA. Several lines of evidence have previously suggested that dopamine-induced changes in motor behavior can be modulated by adenosine analogs acting at the A2 subtype of adenosine receptor in the forebrain. The co-expression of D2 dopamine and A2 adenosine receptors in a subset of striatal cells provides an anatomical basis for dopaminergic-adenosinergic interactions on motor behavior.
引用
收藏
页码:186 / 195
页数:10
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