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Open AccessJournal ArticleDOI

Evidence for multiple AMPA receptor complexes in hippocampal CA1/CA2 neurons.

TLDR
The results show that AMPA receptor complexes with different subunit compositions are present in CA1/CA2 pyramidal neurons and suggest an additional mechanism to regulate receptor expression in neurons.
Abstract
The AMPA receptor, which is involved in most fast glutamatergic transmission in the mammalian brain and is expressed in most neurons, is made up of four subunits, GluR1-4. In situ hybridzation, immunocytochemistry studies, and single-cell PCR analyses show that the number and type of AMPA receptor subunits expressed vary among neuronal populations and that two to four subunits usually are expressed in each neuron. Neurons that express two or more subunits theoretically could produce multiple pentameric receptor complexes that differ in their subunit compositions, and these complexes could be targeted to different synaptic populations. To determine whether a single neuronal population produces multiple AMPA receptor complexes, we used a preparation of CA1/CA2 hippocampal pyramidal neurons and immunoprecipitation with subunit-specific antibodies to characterize the receptor complexes. The CA1/CA2 pyramidal neurons express high levels of GluR1-3 and receive multiple excitatory inputs, offering the possibility that distinct receptor complexes may be assembled and expressed selectively at different synaptic populations. Our results suggest the presence of two major populations of AMPA receptor complexes: those made up of GluR1 and GluR2 and those made up of GluR2 and GluR3. Very few complexes contained both GluR1 and GluR3, whereas approximately 8% of the total AMPA receptor complexes was homomeric GluR1. The integrity of the receptor complex was verified by measuring [3H]AMPA binding activity in the immunoprecipitated fractions. These results show that AMPA receptor complexes with different subunit compositions are present in CA1/CA2 pyramidal neurons and suggest an additional mechanism to regulate receptor expression in neurons.

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The glutamate receptor ion channels

TL;DR: The cloning of cDNAs encoding glutamate receptor subunits, which occurred mainly between 1989 and 1992, stimulated the development of ionotropic glutamate receptors in the brain.
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AMPA Receptor Trafficking and Synaptic Plasticity

TL;DR: The growing literature that supports a critical role for AMPA receptors trafficking in LTP and LTD is reviewed, focusing on the roles proposed for specific AMPA receptor subunits and their interacting proteins.
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Driving AMPA Receptors into Synapses by LTP and CaMKII: Requirement for GluR1 and PDZ Domain Interaction

TL;DR: Results show that LTP and CaMKII activity drive AMPA-Rs to synapses by a mechanism that requires the association between GluR1 and a PDZ domain protein.
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Synaptic plasticity: multiple forms, functions, and mechanisms.

TL;DR: Current understanding of the mechanisms of the major forms of synaptic plasticity at excitatory synapses in the mammalian brain are reviewed.
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The Self-Tuning Neuron: Synaptic Scaling of Excitatory Synapses

TL;DR: Current evidence suggests that neurons detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites.
References
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Journal ArticleDOI

A family of AMPA-selective glutamate receptors

TL;DR: Four cloned cDNAs encoding 900-amino acid putative glutamate receptors with approximately 70 percent sequence identity were isolated from a rat brain cDNA library and in situ hybridization revealed differential expression patterns of the cognate mRNAs throughout the brain.
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Flip and flop: a cell-specific functional switch in glutamate-operated channels of the CNS

TL;DR: These results identify a switch in the molecular and functional properties of glutamate receptors operated by alternative splicing.
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Relative abundance of subunit mRNAs determines gating and Ca2+ permeability of AMPA receptors in principal neurons and interneurons in rat CNS

TL;DR: Analysis of AMPARs in principal neurons and interneurons of hippocampus and neocortex and in auditory relay neurons and Bergmann glial cells indicates that the GluR-B subunit in its flip version determines formation of receptors with relatively slow gating, whereas the GLUR-D subunit promotes assembly of more rapidly gated receptors.
Journal ArticleDOI

Cloning by functional expression of a member of the glutamate receptor family.

TL;DR: A complementary DNA clone is isolated by screening a rat brain cDNA library for expression of kainate-gated ion channels in Xenopus oocytes which on expression in oocytes forms a functional ion channel possessing the electrophysiological and pharmacological properties of the kainates subtype of the glutamate receptor family in the mammalian central nervous system.
Journal ArticleDOI

Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain.

TL;DR: Staining was most prominent in forebrain structures such as the olfactory bulb and tubercle, septal nuclei, amygdaloid complex, hippocampus, induseum griseum, habenula, and interpeduncular nucleus, and in the cerebellum, with limited evidence of stained presynaptic terminals, excepting Bergmann glia.
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