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Pannexin-1 as a potentiator of ligand-gated receptor signaling

机译:Pannexin-1作为配体门控受体信号的增强剂

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摘要

Pannexins are a class of plasma membrane spanning proteins that presumably form a hexameric, non-selective ion channel. Although similar in secondary structure to the connexins, pannexins notably do not form endogenous gap junctions and act as bona fide ion channels. The pannexins have been primarily studied as ATP-release channels, but the overall diversity of their functions is still being elucidated. There is an intriguing theme with pannexins that has begun to develop. In this review we analyze several recent reports that converge on the idea that pannexin channels (namely Panx1) can potentiate ligand-gated receptor signaling. Although the literature remains sparse, this emerging concept appears consistent between both ionotropic and metabotropic receptors of several ligand families
机译:Pannexins是一类质膜跨膜蛋白,可能形成六聚体非选择性离子通道。尽管泛素在二级结构上与连接蛋白相似,但是泛素明显不形成内源性间隙连接,并充当真正的离子通道。 Pannexins主要作为ATP释放通道进行研究,但其功能的总体多样性仍在阐明中。 Pannexins的一个有趣主题已经开始发展。在这篇综述中,我们分析了一些最新的报告,这些报告都集中在pannexin通道(即Panx1)可以增强配体门控受体信号转导的观点上。尽管文献仍然很少,但是这个新兴概念在几个配体家族的离子型和代谢型受体之间似乎是一致的

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