Toggle Main Menu Toggle Search

Open Access padlockePrints

Synapse-Associated Protein 97 Selectively Associates with a Subset of AMPA Receptors Early in their Biosynthetic Pathway

Lookup NU author(s): Dr Claudia Racca

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract

The regulation of AMPA receptors at the postsynaptic membrane is a fundamental component of synaptic plasticity. In the hippocampus, the induction of long-term potentiation increases the delivery of GluR1, a major AMPA receptor subunit in hippocampal pyramidal neurons, to the synaptic plasma membrane through a mechanism that requires the PDZ binding domain of GluR1. Synapse-associated protein 97 (SAP97), a member of the membrane-associated guanylate kinase family, is believed to associate with AMPA receptors (AMPARs) containing the GluR1 subunit, but the functional significance of these interactions is unclear. We investigated the interaction of GluR1 with SAP97, the only PDZ protein known to interact with GluR1. We find that interactions involving SAP97 and GluR1 occur early in the secretory pathway, while the receptors are in the endoplasmic reticulum orcis-Golgi. In contrast, few synaptic receptors associate with SAP97, suggesting that SAP97 dissociates from the receptor complex at the plasma membrane. We also show that internalization of GluR1, as triggered by NMDAR activation, does not require SAP97. These results implicate GluR1–SAP97 interactions in mechanisms underlying AMPA receptor targeting.


Publication metadata

Author(s): Sans N, Racca C, Petralia RS, Wang Y-X, McCallum J, Wenthold RJ

Publication type: Article

Publication status: Published

Journal: The Journal of Neuroscience

Year: 2001

Volume: 21

Issue: 19

Pages: 7506-7516

ISSN (print): 0270-6474

ISSN (electronic): 1529-2401

Publisher: Society for Neuroscience

URL: http://www.jneurosci.org/content/21/19/7506.short


Actions

Find at Newcastle University icon    Link to this publication


Share