Pannexin 1: The Molecular Substrate of Astrocyte "Hemichannels"

被引:304
作者
Iglesias, Rodolfo
Dahl, Gerhard [2 ]
Qiu, Feng [2 ]
Spray, David C.
Scemes, Eliana [1 ]
机构
[1] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Kennedy Ctr, Bronx, NY 10461 USA
[2] Univ Miami, Dept Physiol & Biophys, Miami, FL 33136 USA
基金
美国国家卫生研究院;
关键词
GAP-JUNCTION CHANNELS; CELL-CELL COMMUNICATION; ATP RELEASE; CONNEXIN HEMICHANNELS; GLUTAMATE RELEASE; P2X(7) RECEPTOR; CALCIUM; PERMEABILITY; EXPRESSION; COMPLEX;
D O I
10.1523/JNEUROSCI.6062-08.2009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Purinergic signaling plays distinct and important roles in the CNS, including the transmission of calcium signals between astrocytes. Gap junction hemichannels are among the mechanisms proposed by which astrocytes might release ATP; however, whether the gap junction protein connexin43 (Cx43) forms these "hemichannels" remains controversial. Recently, a new group of proteins, the pannexins, have been shown to form nonselective, high-conductance plasmalemmal channels permeable to ATP, thereby offering an alternative for the hemichannel protein. Here, we provide strong evidence that, in cultured astrocytes, pannexin1 (Panx1) but not Cx43 forms hemichannels. Electrophysiological and fluorescence microscope recordings performed in wild-type and Cx43-null astrocytes did not reveal any differences in hemichannel activity, which was mostly eliminated by treating Cx43-null astrocytes with Panx1-short interfering RNA [Panx1-knockdown (Panx1-KD)]. Moreover, quantification of the amount of ATP released from wild-type, Cx43-null, and Panx1-KD astrocytes indicates that downregulation of Panx1, but not of Cx43, prevented ATP release from these cells.
引用
收藏
页码:7092 / 7097
页数:6
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