Department of Life Sciences, University of Trieste, via Giorgieri 5, 34127, Trieste, Italy.
Adv Exp Med Biol. 2017;1051:7-16. doi: 10.1007/5584_2017_56.
P2X3 receptors are ion channels expressed by autonomic and sensory nerves and specialised in transducing extracellular ATP signals. Structural data, together with functional and biochemical studies, suggest that conformational changes of P2X3 receptors upon agonist binding influence downstream intracellular molecular mechanisms relevant for neuronal responses. Activity of P2X3 receptors is implicated in pain, itch, asthma, cardiovascular dysfunction and other pathologies. The study of these receptors has therefore a large potential in the field of drug development and interdisciplinary efforts could clarify molecular mechanisms controlling P2X3 receptor function in different physiological or pathological contexts.
P2X3 受体是由自主神经和感觉神经表达的离子通道,专门用于转导细胞外 ATP 信号。结构数据,以及功能和生化研究表明,激动剂结合后 P2X3 受体的构象变化影响与神经元反应相关的下游细胞内分子机制。P2X3 受体的活性与疼痛、瘙痒、哮喘、心血管功能障碍和其他病理有关。因此,这些受体的研究在药物开发领域具有很大的潜力,跨学科的努力可以阐明控制 P2X3 受体在不同生理或病理情况下功能的分子机制。