Orioli Elisa, De Marchi Elena, Giuliani Anna Lisa, Adinolfi Elena
Department of Morphology, Surgery and Experimental Medicine, Section of Experimental Pathology, Oncology and Biology, University of Ferrara, Ferrara, Italy.
Curr Med Chem. 2017;24(21):2261-2275. doi: 10.2174/0929867324666170303161659.
P2X7 receptor is an ion channel activated by extracellular adenosine trisphosphate (eATP) that attracted increasing attention for its role in immune reactions, neurobiology and oncology. As receptor for an extracellular ligand, P2X7 activates a series of intracellular signalling pathways mainly via alterations of the ion permeability, but also through formation of a large unselective pore and direct interaction with other proteins. Here we wish to give an overview on the main biochemical paths initiated by P2X7 activation by revising recent and established literature on P2X7-triggered signalling cascades leading to cell death, inflammatory and immune response activation, proliferation and metabolism modulation. We will focus on the well-known P2X7 inflammasome/NF-kB and pro-apoptotic networks but also cover P2X7-activated emerging autophagic, pyroptotic and proliferativeoncogenic pathways, like beclin-1/LC3-II, caspase-11, Akt and VEGF axes.
P2X7受体是一种由细胞外三磷酸腺苷(eATP)激活的离子通道,因其在免疫反应、神经生物学和肿瘤学中的作用而受到越来越多的关注。作为一种细胞外配体的受体,P2X7主要通过改变离子通透性,也通过形成一个大的非选择性孔道以及与其他蛋白质的直接相互作用,激活一系列细胞内信号通路。在这里,我们希望通过回顾最近和已有的关于P2X7触发的信号级联反应导致细胞死亡、炎症和免疫反应激活、增殖和代谢调节的文献,对P2X7激活引发的主要生化途径进行概述。我们将重点关注著名的P2X7炎性小体/NF-κB和促凋亡网络,但也会涵盖P2X7激活的新兴自噬、焦亡和增殖致癌途径,如贝林-1/LC3-II、半胱天冬酶-11、Akt和VEGF轴。