Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition

NMDA (N-methyl-D-aspartate) receptors and non-NMDA receptors represent the two major classes of ion channel-linked glutamate receptors. Unlike the NMDA receptor channels, non-NMDA receptor channels have usually been thought to conduct monovalent cations only. Non-NMDA receptor ion channels that can be gated by kainic acid (KA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) are formed by the glutamate receptor subunits GluR1, GluR2, and GluR3. These subunits were expressed in various combinations in Xenopus oocytes so that their permeability to divalent cations could be studied. At physiological resting potentials, KA and AMPA elicited inward calcium currents in oocytes expressing GluR1, GluR3, and GluR1 plus GluR3. In contrast, oocytes expressing GluR1 plus GluR2 or GluR3 plus GluR2 showed no such permeability. Thus, in neurons expressing certain KA-AMPA receptor subunits, glutamate may trigger calcium-dependent intracellular events by activating non-NMDA receptors.

[1]  R. Miledi,et al.  A calcium-dependent transient outward current in Xenopus laevis oocytes , 1982, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[2]  M E Barish,et al.  A transient calcium‐dependent chloride current in the immature Xenopus oocyte. , 1983, The Journal of physiology.

[3]  R. Miledi,et al.  Chloride current induced by injection of calcium into Xenopus oocytes. , 1984, The Journal of physiology.

[4]  L. Nowak,et al.  Magnesium gates glutamate-activated channels in mouse central neurones , 1984, Nature.

[5]  M. Mayer,et al.  Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones , 1984, Nature.

[6]  M. Mishina,et al.  Location of functional regions of acetylcholine receptor α-subunit by site-directed mutagenesis , 1985, Nature.

[7]  Stephen J. Smith,et al.  NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurones , 1986, Nature.

[8]  M. Mayer,et al.  Permeation and block of N‐methyl‐D‐aspartic acid receptor channels by divalent cations in mouse cultured central neurones. , 1987, The Journal of physiology.

[9]  M. Mayer,et al.  The physiology of excitatory amino acids in the vertebrate central nervous system , 1987, Progress in Neurobiology.

[10]  Samuel Thayer,et al.  The effects of excitatory amino acids on intracellular calcium in single mouse striatal neurons in vitro , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  M. Mayer,et al.  Agonist- and voltage-gated calcium entry in cultured mouse spinal cord neurons under voltage clamp measured using arsenazo III , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  C. Stevens,et al.  Glutamate activates multiple single channel conductances in hippocampal neurons , 1987, Nature.

[13]  T. Bliss,et al.  NMDA receptors - their role in long-term potentiation , 1987, Trends in Neurosciences.

[14]  L. Nowak,et al.  Quisqualate‐ and kainate‐activated channels in mouse central neurones in culture. , 1988, The Journal of physiology.

[15]  D. Choi,et al.  Pharmacology of glutamate neurotoxicity in cortical cell culture: attenuation by NMDA antagonists , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  S N Davies,et al.  Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonists. , 1988, Science.

[17]  L. Nowak,et al.  The role of divalent cations in the N‐methyl‐D‐aspartate responses of mouse central neurones in culture. , 1988, The Journal of physiology.

[18]  G. Collingridge,et al.  Excitatory amino acid receptors in the vertebrate central nervous system. , 1989, Pharmacological reviews.

[19]  J. Olney Excitotoxicity and N‐methyl‐D‐Aspartate receptors , 1989 .

[20]  B. Christensen,et al.  Horizontal cells isolated from catfish retina contain two types of excitatory amino acid receptors. , 1989, Journal of neurophysiology.

[21]  M. Ashburner Drosophila. A laboratory manual. , 1989 .

[22]  N. Dascal,et al.  Two calcium‐activated chloride conductances in Xenopus laevis oocytes permeabilized with the ionophore A23187. , 1989, The Journal of physiology.

[23]  S. Heinemann,et al.  Cloning by functional expression of a member of the glutamate receptor family , 1989, Nature.

[24]  R. Miller,et al.  Regulation of Ca++ influx into striatal neurons by kainic acid. , 1989, The Journal of pharmacology and experimental therapeutics.

[25]  S. Ozawa,et al.  Permeation of calcium through excitatory amino acid receptor channels in cultured rat hippocampal neurones. , 1990, The Journal of physiology.

[26]  S. Kelso,et al.  Apparent desensitization of NMDA responses in xenopus oocytes involves calcium-dependent chloride current , 1990, Neuron.

[27]  A. Ogura,et al.  Non-NMDA receptor mediates cytoplasmic Ca2+ elevation in cultured hippocampal neurones , 1990, Neuroscience Research.

[28]  D. Choi,et al.  The role of glutamate neurotoxicity in hypoxic-ischemic neuronal death. , 1990, Annual review of neuroscience.

[29]  B. Sakmann,et al.  Flip and flop: a cell-specific functional switch in glutamate-operated channels of the CNS. , 1990, Science.

[30]  S. Heinemann,et al.  Cloning of a novel glutamate receptor subunit, GluR5: Expression in the nervous system during development , 1990, Neuron.

[31]  B. Sakmann,et al.  A family of AMPA-selective glutamate receptors. , 1990, Science.

[32]  S. Heinemann,et al.  Molecular cloning and functional expression of glutamate receptor subunit genes. , 1990, Science.

[33]  R. Axel,et al.  A family of glutamate receptor genes: Evidence for the formation of heteromultimeric receptors with distinct channel properties , 1990, Neuron.