P2X7 receptors: Properties and relevance to CNS function
- 27 September 2006
- Vol. 54 (7), 738-746
- https://doi.org/10.1002/glia.20397
Abstract
Among seven members of P2X ionotropic receptors activated by extracellular ATP, the P2X7 subtype is unique in that it can function as a cation channel, a nonselective pore, or even a signaling complex coupled with multiple downstream components. Several roles of P2X7 receptors have been described in CNS cells in the past decade, including release of cytokines and transmitters, modulation of presynaptic transmitter release, and activation of multiple signaling pathways. The finding that P2X7 pores may directly mediate efflux of cytosolic glutamate, GABA, and ATP in glial cells is particularly interesting, as it provides a novel mechanism of glial transmitter release that may play important roles not only in physiological intercellular communication but also in pathological neural injury.Keywords
This publication has 97 references indexed in Scilit:
- Anion channels in astrocytes: Biophysics, pharmacology, and functionGlia, 2006
- Cell cycle regulation of astrocytes by extracellular nucleotides and fibroblast growth factor-2Purinergic Signalling, 2005
- P2X7 receptor-mRNA and -protein in the mouse retina; changes during retinal degeneration in BALBCrds miceNeurochemistry International, 2005
- A Role for Mitogen-activated Protein KinaseErk1/2 Activation and Non-selective Pore Formation in P2X7 Receptor-mediated Thymocyte DeathJournal of Biological Chemistry, 2005
- Characterization of a functional P2X7‐like receptor in cerebellar granule neurons from P2X7 knockout miceFEBS Letters, 2005
- Changes in expression of P2X purinoceptors in rat cerebellum during postnatal developmentDevelopmental Brain Research, 2005
- Identification and characterization of splice variants of the human P2X7 ATP channelBiochemical and Biophysical Research Communications, 2005
- The cytokine IL‐1β transiently enhances P2X7 receptor expression and function in human astrocytesGlia, 2004
- Modulation of intercellular communication in macrophages: possible interactions between GAP junctions and P2 receptorsJournal of Cell Science, 2004
- The isoquinoline derivative KN‐62 a potent antagonist of the P2Z‐receptor of human lymphocytesBritish Journal of Pharmacology, 1997