School of Biological Sciences, University of East Anglia, Norwich, UK.
Channels (Austin). 2013 Jan 1;7(1):43-6. doi: 10.4161/chan.22737. Epub 2012 Dec 6.
P2X receptors are calcium permeable ligand-gated ion channels activated by ATP. Their role as cell surface receptors for extracellular ATP released physiologically by mammalian cells is well established. However, the cellular function of P2X receptor subtypes that populate the membranes of intracellular compartments is not defined. An initial report described how intracellular P2X receptors control the function of the contractile vacuole, an osmoregulatory organelle in Dictyostelium and other protists, and that genetic disruption of P2X receptors severely impaired cell volume control during hypotonic stress. However, later studies refuted a functional role of intracellular P2X receptors in Dictyostelium. Here we provide evidence that the discrepancies reported between the studies are due to the laboratory strain of Dictyostelium employed, which display different phenotypes in response to hypotonic stress and a varied dependency upon P2X receptors for osmoregulation. We use the recent discovery that intracellular P2X receptors are novel calcium release channels to provide some mechanistic insight in an effort to explain why the strain variance may exist.
P2X 受体是钙通透性配体门控离子通道,受 ATP 激活。它们作为细胞表面受体,可与哺乳动物细胞生理性释放的细胞外 ATP 结合,这一作用已得到充分证实。然而,位于细胞内隔室膜上的 P2X 受体亚型的细胞功能尚未明确。最初的报告描述了细胞内 P2X 受体如何控制收缩泡的功能,收缩泡是变形虫和其他原生动物的一种渗透调节细胞器,而 P2X 受体的遗传缺失严重损害了细胞在低渗胁迫下的体积控制。然而,后来的研究否定了细胞内 P2X 受体在变形虫中的功能作用。在这里,我们提供的证据表明,这些研究之间报告的差异是由于所使用的变形虫实验室品系不同,这些品系对低渗胁迫的反应不同,对渗透压调节的 P2X 受体的依赖性也不同。我们利用最近发现的细胞内 P2X 受体是新型钙释放通道这一事实,提供了一些机制上的见解,试图解释为什么会存在这种品系差异。