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      Requirement of AMPA receptor GluR2 phosphorylation for cerebellar long-term depression.

      Science (New York, N.Y.)
      Animals, Calcium, metabolism, Carrier Proteins, Cells, Cultured, Cerebellar Cortex, cytology, physiology, Enzyme Activation, Excitatory Postsynaptic Potentials, Long-Term Synaptic Depression, Mice, Mice, Knockout, Nerve Tissue Proteins, Nuclear Proteins, Nuclear Receptor Coactivator 2, Patch-Clamp Techniques, Phorbol Esters, pharmacology, Phosphorylation, Phosphoserine, Point Mutation, Protein Binding, Protein Kinase C, Purkinje Cells, Receptors, AMPA, genetics, Transcription Factors, Transfection

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          Abstract

          Cerebellar long-term depression (LTD) is a model of synaptic memory that requires protein kinase C (PKC) activation and is expressed as a reduction in the number of postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptors. LTD was absent in cultured cerebellar Purkinje cells from mutant mice lacking the AMPA receptor GluR2 subunit and could be rescued by transient transfection with the wild-type GluR2 subunit. Transfection with a point mutant that eliminated PKC phosphorylation of Ser880 in the carboxy-terminal PDZ ligand of GluR2 failed to restore LTD. In contrast, transfection with a point mutant that mimicked phosphorylation at Ser880 occluded subsequent LTD. Thus, PKC phosphorylation of GluR2 Ser880 is a critical event in the induction of cerebellar LTD.

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