Harden T K, Boyer J L, Nicholas R A
Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill 27599, USA.
Annu Rev Pharmacol Toxicol. 1995;35:541-79. doi: 10.1146/annurev.pa.35.040195.002545.
Extracellular adenine nucleotides interact with P2-purinergic receptors to regulate a broad range of physiological processes. These receptors include the P2Y-, P2U-, P2T-, P2X-, and P2Z-purinergic receptor subtypes. This review focuses on the first three of these receptor subtypes, which couple to G proteins and regulate the inositol lipid, cyclic AMP, and other second-messenger signaling cascades. Both pharmacological data and the occurrence of selectivity of coupling to second-messenger pathways indicate the existence of multiple members in several of the classes of P2-purinergic receptor subtypes. Complementary DNAs cloned for P2Y- and P2U-purinergic receptors predict proteins with seven transmembrane-spanning motifs, typical of that of other G protein-linked receptors.
细胞外腺嘌呤核苷酸与P2 - 嘌呤能受体相互作用,以调节广泛的生理过程。这些受体包括P2Y -、P2U -、P2T -、P2X -和P2Z -嘌呤能受体亚型。本综述聚焦于前三种受体亚型,它们与G蛋白偶联并调节肌醇脂质、环磷酸腺苷及其他第二信使信号级联反应。药理学数据以及与第二信使途径偶联的选择性的存在均表明,P2 - 嘌呤能受体亚型的几个类别中存在多个成员。为P2Y -和P2U -嘌呤能受体克隆的互补DNA预测的蛋白质具有七个跨膜结构域,这是其他G蛋白偶联受体所特有的。