Postsynaptic current mediated by metabotropic glutamate receptors in cerebellar Purkinje cells.

In rat cerebellar slices, repetitive parallel fiber stimulation evokes an inward, postsynaptic current in Purkinje cells with a fast component mediated by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/kainate receptors and a slower component mediated by metabotropic glutamate receptors (mGluR). The mGluR-mediated excitatory postsynaptic current (mGluR-EPSC) is evoked selectively by parallel fiber stimulation; climbing fiber stimulation is ineffective. The mGluR-EPSC is elicited most effectively with increasing frequencies of parallel fiber stimulation, from a threshold of 10 Hz to a maximum response at approximately 100 Hz. The amplitude of the mGluR-EPSC is a linear function of the number of stimulus pulses without any apparent saturation, even with >10 pulses. Thus mGluRs at the parallel fiber-Purkinje cell synapse can function as linear detectors of the number of spikes in a burst of activity in parallel fibers. The mGluR-EPSC is present from postnatal day 15 and persists into adulthood. It is inhibited by the generic mGluR antagonist (RS)-a-methyl-4-carboxyphenylglycine and by the group I mGluR antagonist (RS)-1-aminoindan-1,5-dicarboxylic acid at a concentration selective for mGluR1. Although the intracellular transduction pathway involves a G protein, the putative mediators of mGluR1 (phospholipase C and protein kinase C) are not directly involved, indicating that the mGluR-EPSC studied here is mediated by a different and still unidentified second-messenger pathway. Heparin, a nonselective antagonist of inositol-trisphosphate (IP3) receptors, has no significant effect on the mGluR-EPSC, suggesting that also IP3 might be not required for the response. Buffering intracellular Ca2+ with a high concentration of bis-(o-aminophenoxy)-N,N,N', N'-tetraacetic acid partially inhibits the mGluR-EPSC, indicating that Ca2+ is not directly responsible for the response but that resting Ca2+ levels exert a tonic potentiating effect on the mGluR-EPSC.

[1]  J. Garthwaite,et al.  Synaptic activation of metabotropic glutamate receptors in the parallel Fibre-Purkinje cell pathway in rat cerebellar slices , 1994, Neuroscience.

[2]  T. Knöpfel,et al.  Expression and Coupling to Polyphosphoinositide Hydrolysis of Group I Metabotropic Glutamate Receptors in Early Postnatal and Adult Rat Brain , 1997, The European journal of neuroscience.

[3]  G. Lombardi,et al.  Pharmacological characterization of 1-aminoindan-1,5-dicarboxylic acid, a potent mGluR1 antagonist. , 1997, The Journal of pharmacology and experimental therapeutics.

[4]  J. Garthwaite,et al.  Pharmacological Characterization of Synaptic Transmission through mGluRs in Rat Cerebellar Slices , 1997, Neuropharmacology.

[5]  B. Kemp,et al.  Protein kinase C contains a pseudosubstrate prototope in its regulatory domain. , 1987, Science.

[6]  G. Westbrook,et al.  Distribution of metabotropic glutamate receptor 7 messenger RNA in the developing and adult rat brain , 1995, Neuroscience.

[7]  S. Nakanishi,et al.  Distribution of the mRNA for a metabotropic glutamate receptor (mGluR1) in the central nervous system: An in situ hybridization study in adult and developing rat , 1992, The Journal of comparative neurology.

[8]  P. Somogyi,et al.  Subsynaptic segregation of metabotropic and ionotropic glutamate receptors as revealed by immunogold localization , 1994, Neuroscience.

[9]  J. G. Netzeband,et al.  Metabotropic glutamate receptor agonists alter neuronal excitability and Ca2+ levels via the phospholipase C transduction pathway in cultured Purkinje neurons. , 1997, Journal of neurophysiology.

[10]  R. Nicoll,et al.  Excitatory synaptic currents in Purkinje cells , 1990, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[11]  A. Konnerth,et al.  Synaptic currents in cerebellar Purkinje cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[12]  W. Regehr,et al.  Calcium control of transmitter release at a cerebellar synapse , 1995, Neuron.

[13]  Terri L. Gilbert,et al.  Cloning, expression, and gene structure of a G protein-coupled glutamate receptor from rat brain. , 1991, Science.

[14]  M. Ito,et al.  Messengers mediating long-term desensitization in cerebellar Purkinje cells. , 1990, Neuroreport.

[15]  J. Garthwaite,et al.  Novel synaptic potentials in cerebellar Purkenje cells: Probable mediation by metabotropic glutamate receptors , 1993, Neuropharmacology.

[16]  John Garthwaite,et al.  Frequency detection and temporally dispersed synaptic signal association through a metabotropic glutamate receptor pathway , 1997, Nature.

[17]  S. Nakanishi,et al.  Sequence and expression of a metabotropic glutamate receptor , 1991, Nature.

[18]  S. Wang,et al.  Confocal imaging and local photolysis of caged compounds: Dual probes of synaptic function , 1995, Neuron.

[19]  M. Kano,et al.  Quisqualate receptors are specifically involved in cerebellar synaptic plasticity , 1987, Nature.

[20]  D. Linden,et al.  Trans-ACPD, a metabotropic receptor agonist, produces calcium mobilization and an inward current in cultured cerebellar Purkinje neurons. , 1994, Journal of neurophysiology.

[21]  A. Konnerth,et al.  Synaptic‐ and agonist‐induced excitatory currents of Purkinje cells in rat cerebellar slices. , 1991, The Journal of physiology.

[22]  N. Hartell Induction of cerebellar long-term depression requires activation of glutamate metabotropic receptors. , 1994, Neuroreport.

[23]  D. Lovinger,et al.  Rat group I metabotropic glutamate receptors inhibit neuronal Ca2+ channels via multiple signal transduction pathways in HEK 293 cells. , 1998, Journal of neurophysiology.

[24]  S. Nakanishi,et al.  Antibodies inactivating mGluR1 metabotropic glutamate receptor block long-term depression in cultured Purkinje cells , 1994, Neuron.

[25]  B. Gähwiler,et al.  Trans‐ACPD-induced Ca2+ signals in cerebellar Purkinje cells , 1991, Neuroreport.

[26]  J. Penney,et al.  Metabotropic glutamate receptors are differentially regulated during development , 1994, Neuroscience.

[27]  M. Sakurai Calcium is an intracellular mediator of the climbing fiber in induction of cerebellar long-term depression. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[28]  K. Mikoshiba,et al.  Characterization of Metabotropic Glutamate Receptors in Cultured Purkinje Cells , 1993, Annals of the New York Academy of Sciences.

[29]  A. Konnerth,et al.  Intradendritic release of calcium induced by glutamate in cerebellar purkinje cells , 1991, Neuron.

[30]  S. Nakanishi,et al.  Distributions of the mRNAs for L‐2‐amino‐4‐phosphonobutyrate‐sensitive metabotropic glutamate receptors, mGluR4 and mGluR7, in the rat brain , 1995, The Journal of comparative neurology.

[31]  T. Hirano,et al.  Critical role of postsynaptic calcium in cerebellar long‐term depression , 1994, Neuroreport.

[32]  M. Dickinson,et al.  A long-term depression of AMPA currents in cultured cerebellar purkinje neurons , 1991, Neuron.

[33]  A. Konnerth,et al.  Brief dendritic calcium signals initiate long-lasting synaptic depression in cerebellar Purkinje cells. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[34]  A. N. van den Pol,et al.  Developmental regulation of the hypothalamic metabotropic glutamate receptor mGluR1 , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  R. Duvoisin,et al.  The metabotropic glutamate receptors: Structure and functions , 1995, Neuropharmacology.

[36]  S. Tonegawa,et al.  Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice , 1994, Cell.

[37]  G. Collingridge,et al.  Motor deficit and impairment of synaptic plasticity in mice lacking mGluR1 , 1994, Nature.

[38]  P. Willems,et al.  Effect of the aminosteroid, U73122, on Ca2+ uptake and release properties of rat liver microsomes. , 1995, European journal of biochemistry.

[39]  D. Linden,et al.  Participation of postsynaptic PKC in cerebellar long-term depression in culture. , 1991, Science.

[40]  J. G. Netzeband,et al.  Ca2+ signaling pathways linked to glutamate receptor activation in the somatic and dendritic regions of cultured cerebellar purkinje neurons. , 1996, Journal of neurophysiology.

[41]  W G Regehr,et al.  Calcium transients in cerebellar granule cell presynaptic terminals. , 1995, Biophysical journal.

[42]  O. Garaschuk,et al.  Fractional calcium current through neuronal AMPA-receptor channels with a low calcium permeability , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[43]  K. Mikoshiba,et al.  Pharmacological and immunocytochemical characterization of metabotropic glutamate receptors in cultured Purkinje cells , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  D. Condorelli,et al.  Development profile of metabotropic glutamate receptor mRNA in rat brain. , 1992, Molecular pharmacology.

[45]  R. Llinás,et al.  Electrophysiological properties of in vitro Purkinje cell dendrites in mammalian cerebellar slices. , 1980, The Journal of physiology.

[46]  T. Knöpfel,et al.  Responses to Metabotropic Glutamate Receptor Activation in Cerebellar Purkinje Cells: Induction of an Inward Current , 1992, The European journal of neuroscience.