Signaling at Purinergic P2X Receptors

被引:438
|
作者
Surprenant, Annmarie [1 ]
North, R. Alan [1 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
ATP; ligand-gated ion channels; transgenic mice; structure-function; mutagenesis; cell signaling; ATP-GATED P2X(2); FIRST TRANSMEMBRANE DOMAIN; BINDING-SITE; TUBULOGLOMERULAR FEEDBACK; EXTRACELLULAR ATP; IN-VITRO; NEUROPATHIC PAIN; MICE LACKING; ION-CHANNEL; NEUROHYPOPHYSEAL TERMINALS;
D O I
10.1146/annurev.physiol.70.113006.100630
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
P2X receptors are membrane cation channels gated by extracellular ATP. Seven P2X receptor subunits (P2X(1-7)) are widely distributed in excitable and nonexcitable cells of vertebrates. They play key roles in inter alia afferent signaling (including pain), regulation of renal blood flow, vascular endothelium, and inflammatory responses. We summarize the evidence for these and other roles, emphasizing experimental work with selective receptor antagonists or with knockout mice. The receptors are trimeric membrane proteins: Studies of the biophysical properties of mutated subunits expressed in heterologous cells have indicated parts of the subunits involved in ATP binding, ion permeation (including calcium permeability), and membrane trafficking. We review our current understanding of the molecular properties of P2X receptors, including how this understanding is informed by the identification of distantly related P2X receptors in simple eukaryotes.
引用
收藏
页码:333 / 359
页数:27
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