Pannexin1 is part of the pore forming unit of the P2X7 receptor death complex

被引:380
作者
Locovei, Silviu
Scemes, Eliana
Qiu, Feng
Spray, David C.
Dahl, Gerhard
机构
[1] Univ Miami, Sch Med, Dept Physiol & Biophys, Miami, FL 33136 USA
[2] Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
关键词
Pannexin; P2X(7); pore; siRNA; ion channel;
D O I
10.1016/j.febslet.2006.12.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purinergic receptor P2X(7) is part of a complex signaling mechanism participating in a variety of physiological and pathological processes. Depending on the activation scheme, P2X(7) receptors in vivo are non-selective cation channels or form large pores that can mediate apoptotic cell death. Expression of P2X(7)R in Xenopus oocytes results exclusively in formation of a non-selective cation channel. However, here we show that coexpression of P2X(7)R with pannexin1 in oocytes leads to the complex response seen in many mammalian cells, including cell death with prolonged ATP application. While the cation channel activity is resistant to carbenoxolone treatment, this gap junction and hemichannel blocking drug suppressed the currents induced by ATP in pannexin1/P2X(7)R co-expressing cells. Thus, pannexin1 appears to be the molecular substrate for the permeabilization pore (or death receptor channel) recruited into the P2X(7)R signaling complex. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:483 / 488
页数:6
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