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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Nature Neurosciencearrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Nature Neuroscience
Article . 2005 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
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TARP γ-8 controls hippocampal AMPA receptor number, distribution and synaptic plasticity

Authors: Nathalie, Rouach; Keith, Byrd; Ronald S, Petralia; Guillermo M, Elias; Hillel, Adesnik; Susumu, Tomita; Siavash, Karimzadegan; +3 Authors

TARP γ-8 controls hippocampal AMPA receptor number, distribution and synaptic plasticity

Abstract

Synaptic plasticity involves activity-dependent trafficking of AMPA-type glutamate receptors. Numerous cytoplasmic scaffolding proteins are postulated to control AMPA receptor trafficking, but the detailed mechanisms remain unclear. Here, we show that the transmembrane AMPA receptor regulatory protein (TARP) gamma-8, which is preferentially expressed in the mouse hippocampus, is important for AMPA receptor protein levels and extrasynaptic surface expression. By controlling the number of AMPA receptors, gamma-8 is also important in long-term potentiation, but not long-term depression. This study establishes gamma-8 as a critical protein for basal AMPA receptor expression and localization at extrasynaptic sites in the hippocampus and raises the possibility that TARP-dependent control of AMPA receptors during synapse development and plasticity may be widespread.

Keywords

Mice, Knockout, Kainic Acid, Neuronal Plasticity, Blotting, Western, Green Fluorescent Proteins, Excitatory Postsynaptic Potentials, Dose-Response Relationship, Radiation, In Vitro Techniques, Blotting, Northern, Hippocampus, Immunohistochemistry, Electric Stimulation, Membrane Potentials, Mice, Inbred C57BL, Blotting, Southern, Mice, Gene Expression Regulation, Excitatory Amino Acid Agonists, Animals, Microscopy, Immunoelectron

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Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
257
Top 1%
Top 10%
Top 1%