Extracellular zinc and ATP-gated P2X receptor calcium entry channels: New zinc receptors as physiological sensors and therapeutic targets

被引:16
|
作者
Schwiebert E.M. [1 ,2 ,3 ,4 ]
Liang L. [1 ,3 ]
Cheng N.-L. [1 ,3 ]
Williams C.R. [1 ]
Olteanu D. [1 ,4 ]
Welty E.A. [1 ,3 ]
Zsembery A. [1 ,3 ,5 ]
机构
[1] Department of Physiology and Biophysics, University of Alabama at Birmingham, Birmingham
[2] Department of Cell Biology, University of Alabama at Birmingham, Birmingham
[3] Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham
[4] Recessive Polycystic Kidney Disease Core Center, University of Alabama at Birmingham, Birmingham
[5] Institute of Human Physiology and Clinical Experimental Research, Semmelweis University, Budapest
基金
美国国家卫生研究院; 匈牙利科学研究基金会;
关键词
β; cells; Calcium; Cystic fibrosis; Diabetes; Epithelia; P2X receptors; Polycystic kidney disease; Sensors; Zinc;
D O I
10.1007/s11302-005-0777-7
中图分类号
学科分类号
摘要
In this review, we focus on two attributes of P2X receptor channel function, one essential and one novel. First, we propose that P2X receptors are extracellular sensors as well as receptors and ion channels. In particular, the large extracellular domain (that comprises 70% of the molecular mass of the receptor channel protein) lends itself to be a cellular sensor. Moreover, its exquisite sensitivity to extracellular pH, ionic strength, and multiple ligands evokes the function of a sensor. Second, we propose that P2X receptors are extracellular zinc receptors as well as receptors for nucleotides. We provide novel data in multiple publications and illustrative data in this invited review to suggest that zinc triggers ATP-independent activation of P2X receptor channel function. In this light, P2X receptors are the cellular site of integration between autocrine and paracrine zinc signaling and autocrine and paracrine purinergic signaling. P2X receptors may sense changes in these ligands as well as in extracellular pH and ionic strength and transduce these sensations via calcium and/or sodium entry and changes in membrane potential. © Springer 2005.
引用
收藏
页码:299 / 310
页数:11
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