A new class of ligand-gated ion channel defined by P2X receptor for extracellular ATP
- 1 October 1994
- journal article
- Published by Springer Nature in Nature
- Vol. 371 (6497) , 516-519
- https://doi.org/10.1038/371516a0
Abstract
Extracellular ATP exerts its effects through P2 purinoceptors: these are ligand-gated ion channels (P2x) or G-protein-coupled receptors (P2Y, P2U). ATP at P2x receptors mediates synaptic transmission between neurons and from neurons to smooth muscle, being responsible, for example, for sympathetic vasoconstriction in small arteries and arterioles. We have now cloned a complementary DNA encoding the P2x receptor from rat vas deferens and expressed it in Xenopus oocytes and mammalian cells. ATP activates a cation-selective ion channel with relatively high calcium permeability. Structural predictions suggest that the protein (399 amino acids long) is mostly extracellular and contains only two transmembrane domains plus a pore-forming motif which resembles that of potassium channels. The P2x receptor thus defines a new family of ligand-gated ion channels.Keywords
This publication has 28 references indexed in Scilit:
- G protein-coupled receptors for ATP and other nucleotides: a new receptor familyTrends in Pharmacological Sciences, 1994
- ATP receptor-mediated synaptic currents in the central nervous systemNature, 1992
- ATP mediates excitatory synaptic transmission in mammalian neuronesBritish Journal of Pharmacology, 1992
- ATP mediates fast synaptic transmission in mammalian neuronsNature, 1992
- Vasoconstriction of guinea‐pig submucosal arterioles following sympathetic nerve stimulation is mediated by the release of ATPBritish Journal of Pharmacology, 1992
- Pharmacology and electrophysiology of ATP-activated ion channelsTrends in Pharmacological Sciences, 1992
- Overview: Purinergic MechanismsAnnals of the New York Academy of Sciences, 1990
- ATP-Activated Channels in Excitable CellsPublished by Springer Nature ,1990
- Sympathetic purinergic transmission in small blood vesselsTrends in Pharmacological Sciences, 1988
- A novel receptor-operated Ca2+-permeable channel activated by ATP in smooth muscleNature, 1987