Coupling of P2Y receptors to G proteins and other signaling pathways.

Laurie Erb, Gary A Weisman
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引用次数: 157

Abstract

P2Y receptors are G protein-coupled receptors (GPCRs) that are activated by adenine and uridine nucleotides and nucleotide sugars. There are eight subtypes of P2Y receptors (P2Y1, P2Y2, P2Y4, P2Y6, P2Y11, P2Y12, P2Y13, and P2Y14), which activate intracellular signaling cascades to regulate a variety of cellular processes, including proliferation, differentiation, phagocytosis, secretion, nociception, cell adhesion, and cell migration. These signaling cascades operate mainly by the sequential activation or deactivation of heterotrimeric and monomeric G proteins, phospholipases, adenylyl and guanylyl cyclases, protein kinases, and phosphodiesterases. In addition, there are numerous ion channels, cell adhesion molecules, and receptor tyrosine kinases that are modulated by P2Y receptors and operate to transmit an extracellular signal to an intracellular response.

P2Y受体与G蛋白和其他信号通路的偶联。
P2Y受体是G蛋白偶联受体(gpcr),可被腺嘌呤和尿嘧啶核苷酸及核苷酸糖激活。P2Y受体有8种亚型(P2Y1、P2Y2、P2Y4、P2Y6、P2Y11、P2Y12、P2Y13和P2Y14),它们激活细胞内信号级联,调节多种细胞过程,包括增殖、分化、吞噬、分泌、伤害感受、细胞粘附和细胞迁移。这些信号级联主要通过异三聚体和单体G蛋白、磷脂酶、腺苷酸环化酶和胍基环化酶、蛋白激酶和磷酸二酯酶的顺序激活或失活来运作。此外,还有许多离子通道、细胞粘附分子和受体酪氨酸激酶受P2Y受体调节,并将细胞外信号传递到细胞内反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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