Research in my laboratory focuses on the properties and molecular mechanisms of synaptic plasticity at mammalian cortical glutamatergic synapses. Our primary approach is to use electrophysiological recordings from neurons in brain slices. This is combined with techniques such as viral expression of genes of interest in slices, 2 photon calcium imaging and glutamate uncaging.? We are investigating the roles of phosphorylation and trafficking motifs and of proteins that interact with AMPA, NMDA and kainate receptor subunits in the functional regulation of these receptors. We use four primary approaches: 1) acute blockade of specific interactions by introducing peptides into individual neurons, 2) chronic over expression of constructs of interest using Sindbis virus in cultured slices, 3) shRNA knock down using Lenti virus in cultured slices, and 4) acute slice electrophysiology in transgenic mice. The effects of these manipulations are then assessed by investigating changes in AMPA, kainate or NMDA receptor-mediated synaptic transmission and plasticity. ? Current studies are focusing on PICK1. We have found that PICK1, which interacts directly with AMPA receptors at synapses and is a calcium-sensitive protein, is critical for NMDA receptor-dependent long-term potentiation (LTP) in hippocampus. Moreover, PICK1 mediates a novel activity-dependent switch in the GluR2 subunit composition of AMPA receptors during LTP, rendering them calcium-permeable. This novel mechanism provides a potential process by which the calcium-permeability of AMPA receptors is regulated during neurological disorders such as cerebral ischemia. ? We are also characterizing the function of novel phosphorylation sites in the regulation of NMDA and kainate receptor trafficking. Recently we have defined a number of new PKA and PKC phosphorylation sites on the kainate receptor GluR6 subunit and find that some of these regulate endocytocis.? Therefore, these studies are defining novel mechanisms regulating the expression and function of glutamate receptors at synapses that are critical for the expression of forms of long-term synaptic plasticity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Intramural Research (Z01)
Project #
1Z01NS003035-01
Application #
7594726
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2007
Total Cost
$1,211,608
Indirect Cost
City
State
Country
United States
Zip Code
Isaac, John T R; Ashby, Michael; McBain, Chris J (2007) The role of the GluR2 subunit in AMPA receptor function and synaptic plasticity. Neuron 54:859-71