Purine and pyrimidine receptors

被引:742
作者
Burnstock, G. [1 ]
机构
[1] UCL Royal Free & Univ Coll, Sch Med, Autonom Neurosci Ctr, London NW3 2PF, England
关键词
cloned receptors; gene regulation; G protein-coupled receptors; heteromultimers; ion channel receptors; P1; receptor; P2X receptor; P2Y receptor;
D O I
10.1007/s00018-007-6497-0
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
Adenosine 5'-triphosphate (ATP), in addition to its intracellular roles, acts as an extracellular signalling molecule via a rich array of receptors, which have been cloned and characterised. P1 receptors are selective for adenosine, a breakdown product of ATP, produced after degradation by ectonucleotidases. Four subtypes have been identified, A(1), A(2A), A(2B) and A(3) receptors. P2 receptors are activated by purines and some subtypes also by pyrimidines. P2X receptors are ligand-gated ion channel receptors and seven subunits have been identified, which form both homomultimers and heteromultimers. P2Y receptors are G protein-coupled receptors, and eight subtypes have been cloned and characterised to date.
引用
收藏
页码:1471 / 1483
页数:13
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