Involvement of the Secretory Pathway for AMPA Receptors in NMDA-Induced Potentiation in Hippocampus

A chemical form of synaptic potentiation was produced with a brief bath application of NMDA to rat hippocampal slices. Two methods were used to assess changes in membrane-bound AMPA receptors. Traditional subcellular fractionation was used to isolate synaptic membranes; alternatively, membrane receptors were cross-linked with the membrane-impermeable reagent bis(sulfosuccinimidyl) suberate, and levels of nonmembrane receptors were determined. In both cases, Western blots were used to determine the content of receptor subunits in various subcellular fractions. NMDA-induced potentiation was associated with increased levels of glutamate receptor 1 (GluR1) and GluR2/3 subunits of AMPA receptors in synaptic membrane preparations, whereas no change was observed in whole homogenates. Both KN-62, an inhibitor of calcium/calmodulin kinase, and calpain inhibitor III, a calpain inhibitor, inhibited NMDA-induced potentiation and changes in GluR1 and GluR2/3 subunits of AMPA receptors. Brefeldin A (BFA) inhibits protein trafficking between the Golgi apparatus and cell membranes. Pretreatment of hippocampal slices with BFA significantly decreased NMDA-induced potentiation and completely prevented an NMDA-induced increase in GluR1 levels in membrane fractions. Thus, the levels of GluR1 and GluR2/3 subunits of AMPA receptors are rapidly upregulated in synaptic membranes under conditions associated with potentiation of synaptic responses, and this upregulation requires a functional secretory pathway.

[1]  R. Nicoll,et al.  Synaptic plasticity and dynamic modulation of the postsynaptic membrane , 2000, Nature Neuroscience.

[2]  Roberto Malinow,et al.  LTP mechanisms: from silence to four-lane traffic , 2000, Current Opinion in Neurobiology.

[3]  G. Turrigiano AMPA Receptors Unbound Membrane Cycling and Synaptic Plasticity , 2000, Neuron.

[4]  R. Malinow,et al.  Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction. , 2000, Science.

[5]  D. Linden,et al.  Expression of Cerebellar Long-Term Depression Requires Postsynaptic Clathrin-Mediated Endocytosis , 2000, Neuron.

[6]  Yu Tian Wang,et al.  Regulation of AMPA Receptor–Mediated Synaptic Transmission by Clathrin-Dependent Receptor Internalization , 2000, Neuron.

[7]  N. Toni,et al.  LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite , 1999, Nature.

[8]  R. Nicoll,et al.  Dynamin-dependent endocytosis of ionotropic glutamate receptors. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Mark von Zastrow,et al.  Role of AMPA Receptor Cycling in Synaptic Transmission and Plasticity , 1999, Neuron.

[10]  J. Isaac,et al.  Silent glutamatergic synapses in the mammalian brain. , 1999, Canadian journal of physiology and pharmacology.

[11]  R. Wenthold,et al.  Differential Distribution of Intracellular Glutamate Receptors in Dendrites , 1999, The Journal of Neuroscience.

[12]  K. Svoboda,et al.  Rapid spine delivery and redistribution of AMPA receptors after synaptic NMDA receptor activation. , 1999, Science.

[13]  G. Collingridge,et al.  Surface Expression of AMPA Receptors in Hippocampal Neurons Is Regulated by an NSF-Dependent Mechanism , 1999, Neuron.

[14]  M. Krug,et al.  Glycosylation of proteins during a critical time window is necessary for the maintenance of long-term potentiation in the hippocampal CA1 region , 1999, Neuroscience.

[15]  F. Engert,et al.  Dendritic spine changes associated with hippocampal long-term synaptic plasticity , 1999, Nature.

[16]  K. Svoboda,et al.  Rapid dendritic morphogenesis in CA1 hippocampal dendrites induced by synaptic activity. , 1999, Science.

[17]  Mark F Bear,et al.  NMDA Induces Long-Term Synaptic Depression and Dephosphorylation of the GluR1 Subunit of AMPA Receptors in Hippocampus , 1998, Neuron.

[18]  R. Malinow,et al.  Calcium-Evoked Dendritic Exocytosis in Cultured Hippocampal Neurons. Part I: Trans-Golgi Network-Derived Organelles Undergo Regulated Exocytosis , 1998, The Journal of Neuroscience.

[19]  R. Malinow,et al.  Calcium-Evoked Dendritic Exocytosis in Cultured Hippocampal Neurons. Part II: Mediation by Calcium/Calmodulin-Dependent Protein Kinase II , 1998, The Journal of Neuroscience.

[20]  R. Huganir,et al.  Interaction of the N-Ethylmaleimide–Sensitive Factor with AMPA Receptors , 1998, Neuron.

[21]  S. Shenolikar,et al.  Gating of CaMKII by cAMP-regulated protein phosphatase activity during LTP. , 1998, Science.

[22]  M. Baudry,et al.  High‐ and Low‐Affinity α‐[3H]Amino‐3‐Hydroxy‐5‐Methylisoxazole‐4‐Propionic Acid ([3H]AMPA) Binding Sites Represent Immature and Mature Forms of AMPA Receptors and Are Composed of Differentially Glycosylated Subunits , 1998, Journal of neurochemistry.

[23]  G. Lynch,et al.  Effects of aniracetam after LTP induction are suggestive of interactions on the kinetics of the AMPA receptor channel , 1998, Brain Research.

[24]  R. Nicoll,et al.  Postsynaptic membrane fusion and long-term potentiation. , 1998, Science.

[25]  G Tocco,et al.  Glycine-induced long-term potentiation is associated with structural and functional modifications of alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionic acid receptors. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[26]  T W Berger,et al.  Novel expression mechanism for synaptic potentiation: alignment of presynaptic release site and postsynaptic receptor. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[27]  T. Soderling,et al.  Surface Expression of the AMPA Receptor Subunits GluR1, GluR2, and GluR4 in Stably Transfected Baby Hamster Kidney Cells , 1997, Journal of neurochemistry.

[28]  K M Harris,et al.  Three-Dimensional Organization of Smooth Endoplasmic Reticulum in Hippocampal CA1 Dendrites and Dendritic Spines of the Immature and Mature Rat , 1997, The Journal of Neuroscience.

[29]  J. Isaac,et al.  Expression mechanisms of long-term potentiation in the hippocampus , 1996, Journal of Physiology-Paris.

[30]  P. Somogyi,et al.  High-resolution immunogold localization of AMPA type glutamate receptor subunits at synaptic and non-synaptic sites in rat hippocampus , 1995, Neuroscience.

[31]  R. Nicoll,et al.  Calcium/calmodulin-dependent kinase II and long-term potentiation enhance synaptic transmission by the same mechanism. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[32]  J. Isaac,et al.  Evidence for silent synapses: Implications for the expression of LTP , 1995, Neuron.

[33]  G. Lynch,et al.  Proteolysis of spectrin by calpain accompanies theta-burst stimulation in cultured hippocampal slices. , 1995, Brain research. Molecular brain research.

[34]  R. Malinow,et al.  Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice , 1995, Nature.

[35]  J. Henley Subcellular localization and molecular pharmacology of distinct populations of [3H]‐AMPA binding sites in rat hippocampus , 1995, British journal of pharmacology.

[36]  R. Malinow,et al.  Potentiated transmission and prevention of further LTP by increased CaMKII activity in postsynaptic hippocampal slice neurons. , 1994, Science.

[37]  P. Somogyi,et al.  Synaptic and nonsynaptic localization of the GluR1 subunit of the AMPA- type excitatory amino acid receptor in the rat cerebellum , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[38]  M E Martone,et al.  Three-dimensional visualization of the smooth endoplasmic reticulum in Purkinje cell dendrites , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[39]  G Tocco,et al.  Postsynaptic factors in the expression of long-term potentiation (LTP): increased glutamate receptor binding following LTP induction in vivo. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[40]  G. Lynch,et al.  Waveform analysis suggests that LTP alters the kinetics of synaptic receptor channels , 1993, Brain Research.

[41]  G Lynch,et al.  Channel gating kinetics and synaptic efficacy: a hypothesis for expression of long-term potentiation. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[42]  M. Baudry,et al.  High concentrations of glycine induce long-lasting changes in synaptic efficacy in rat hippocampal slices , 1993, Neuroscience Letters.

[43]  J. Lippincott-Schwartz,et al.  Brefeldin A: insights into the control of membrane traffic and organelle structure , 1992, The Journal of cell biology.

[44]  M. Wayner,et al.  Calpain inhibitors block long-term potentiation , 1990, Brain Research.

[45]  G. Lynch,et al.  Development of hippocampal long-term potentiation is reduced by recently introduced calpain inhibitors , 1990, Brain Research.

[46]  R. Tsien,et al.  Inhibition of postsynaptic PKC or CaMKII blocks induction but not expression of LTP. , 1989, Science.

[47]  G. Lynch,et al.  Long-lasting physiological effects of bath applied N-methyl-d-aspartate , 1989, Brain Research.

[48]  K. Harris,et al.  Dendritic spines of rat cerebellar Purkinje cells: serial electron microscopy with reference to their biophysical characteristics , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[49]  R. Nicoll,et al.  NMDA application potentiates synaptic transmission in the hippocampus , 1988, Nature.

[50]  Y. Misumi,et al.  Brefeldin A arrests the intracellular transport of a precursor of complement C3 before its conversion site in rat hepatocytes , 1987, FEBS letters.

[51]  Y. Misumi,et al.  Novel blockade by brefeldin A of intracellular transport of secretory proteins in cultured rat hepatocytes. , 1986, The Journal of biological chemistry.

[52]  G. Lynch,et al.  The biochemistry of memory: a new and specific hypothesis. , 1984, Science.

[53]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

[54]  M. Baudry,et al.  Posttranslational regulation of ionotropic glutamate receptors and synaptic plasticity. , 1998, International review of neurobiology.

[55]  G. Lynch,et al.  Receptor changes and LTP: An analysis using aniracetam, a drug that reversibly modifies glutamate (AMPA) receptors , 1992, Hippocampus.