von Kügelgen I, Wetter A
Department of Pharmacology, University of Bonn, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 2000 Nov;362(4-5):310-23. doi: 10.1007/s002100000310.
Membrane-bound P2-receptors mediate the actions of extracellular nucleotides in cell-to-cell signalling. P2X-receptors are ligand-gated ion channels, whereas P2Y-receptors belong to the superfamily of G-protein-coupled receptors. So far, the P2Y family is composed of eight cloned and functionally defined subtypes. Five of them (P2Y1, P2Y2, P2Y4, P2Y6 and P2Y11) are present in human tissues. The P2Y3-, p2y8- and tp2y-receptors may be species orthologues. The principal physiological agonists of the cloned human P2Y-receptors are ADP (P2Y1), UTP/ATP (P2Y2), UTP (P2Y4), UDP (P2Y6) and ATP (P2Y11). The rat P2Y4-receptor is activated by both UTP and ATP. Specific patterns of polar amino acid residues in the exofacial portions of transmembrane domains (TMs) 6 and 7 of the P2Y-receptors may account for the ligand specificity of the subtypes. Suramin acts as an antagonist at most P2Y-receptors with the exception of P2Y4- and tp2y-receptors. PPADS has been shown to block P2Y1-, the human P2Y4- and P2Y6-receptors. The nucleotide analogue 2'-deoxy-N6-methyladenosine-3',5'-bisphosphate (MRS 2179), in contrast, seems to be a potent and selective antagonist at the P2Y1-receptor. All cloned and functionally expressed P2Y-receptors are able to couple to phospholipase C. The P2Y11-receptor mediates in addition a stimulation of adenylate cyclase and the tp2y-receptor an inhibition of this signal transduction pathway. Other functionally defined subtypes, e.g., the receptor mediating an inhibition of adenylate cyclase in blood platelets, are not yet cloned. The distribution of P2Y1 mRNA is widespread. The receptor plays a crucial role in blood platelet aggregation and mediates the adenine nucleotide-induced release of the endothelium-derived relaxing factor nitric oxide. P2Y1-receptors may also be involved in the modulation of neuro-neural signalling transmission. P2Y2 transcripts are abundantly distributed. One important example for its functional role is the control of chloride ion fluxes in airway epithelia. The P2Y4-receptor is highly expressed in the placenta. The distribution of the P2Y6-receptor is widespread including heart, blood vessels and brain. The P2Y11-receptor may play a role in the differentiation of immunocytes.
膜结合型P2受体介导细胞间信号传导中细胞外核苷酸的作用。P2X受体是配体门控离子通道,而P2Y受体属于G蛋白偶联受体超家族。到目前为止,P2Y家族由8种已克隆且功能明确的亚型组成。其中5种(P2Y1、P2Y2、P2Y4、P2Y6和P2Y11)存在于人体组织中。P2Y3、P2Y8和P2Y受体可能是物种同源物。已克隆的人P2Y受体的主要生理激动剂是ADP(P2Y1)、UTP/ATP(P2Y2)、UTP(P2Y4)、UDP(P2Y6)和ATP(P2Y11)。大鼠P2Y4受体可被UTP和ATP激活。P2Y受体跨膜结构域(TMs)6和7胞外侧部分极性氨基酸残基的特定模式可能解释了各亚型的配体特异性。除P2Y4和P2Y受体外,苏拉明在大多数P2Y受体上起拮抗剂作用。已证明PPADS可阻断P2Y1、人P2Y4和P2Y6受体。相比之下,核苷酸类似物2'-脱氧-N6-甲基腺苷-3',5'-双磷酸(MRS 2179)似乎是P2Y1受体的强效选择性拮抗剂。所有已克隆并功能性表达的P2Y受体都能够与磷脂酶C偶联。此外,P2Y11受体介导腺苷酸环化酶的刺激,而P2Y受体介导该信号转导途径的抑制。其他功能明确的亚型,例如介导血小板中腺苷酸环化酶抑制的受体,尚未被克隆。P2Y1 mRNA分布广泛。该受体在血小板聚集中起关键作用,并介导腺嘌呤核苷酸诱导的内皮源性舒张因子一氧化氮的释放。P2Y1受体也可能参与神经-神经信号传递的调节。P2Y2转录本分布丰富。其功能作用的一个重要例子是气道上皮中氯离子通量的控制。P2Y4受体在胎盘中高度表达。P2Y6受体分布广泛,包括心脏、血管和大脑。P2Y11受体可能在免疫细胞分化中起作用。