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嘌呤和嘧啶受体。

Purine and pyrimidine receptors.

作者信息

Burnstock G

机构信息

Autonomic Neuroscience Centre, Royal Free and University College Medical School, London, UK.

出版信息

Cell Mol Life Sci. 2007 Jun;64(12):1471-83. doi: 10.1007/s00018-007-6497-0.

Abstract

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.

摘要

5'-三磷酸腺苷(ATP)除了在细胞内发挥作用外,还通过一系列已被克隆和鉴定的丰富受体作为细胞外信号分子发挥作用。P1受体对腺苷具有选择性,腺苷是ATP的一种分解产物,由胞外核苷酸酶降解后产生。已鉴定出四种亚型,即A(1)、A(2A)、A(2B)和A(3)受体。P2受体可被嘌呤激活,一些亚型也可被嘧啶激活。P2X受体是配体门控离子通道受体,已鉴定出七个亚基,它们可形成同多聚体和异多聚体。P2Y受体是G蛋白偶联受体,迄今为止已克隆并鉴定出八个亚型。

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