The GluA1 cytoplasmic tail regulates intracellular AMPA receptor trafficking and synaptic transmission onto dentate gyrus GABAergic interneurons, gating response to novelty

TL;DR

This study shows how a part of the GluA1 protein controls AMPA receptor trafficking and affects brain activity and behavior in mice.

Contribution

The study reveals the GluA1 cytoplasmic tail's role in AMPAR trafficking and synaptic transmission in a cell-specific manner.

Findings

GluA1 CTD truncation alters AMPAR subunit levels and trafficking.

ΔCTD GluA1 mice show exaggerated novelty-induced hyperlocomotion and DG GC hyperactivity.

AMPAR EPSCs onto DG GABAergic interneurons are significantly reduced.

Abstract

The GluA1 subunit, encoded by the putative schizophrenia-associated gene GRIA1, is required for activity-regulated AMPA receptor (AMPAR) trafficking, and plays a key role in cognitive and affective function. The cytoplasmic, carboxy-terminal domain (CTD) is highly sequence-divergent across AMPAR subunits, and has received considerable attention for its role during long-term potentiation (LTP) at CA1 pyramidal neuron synapses. However, its function at other synapses and, more broadly, its contribution to different GluA1-dependent processes, is poorly understood. Here, we used mice with a constitutive truncation of the GluA1 CTD to dissect its role regulating AMPAR localization and function as well as its contribution to cognitive and affective processes. We found that GluA1 CTD truncation affected AMPAR subunit levels and intracellular trafficking. ΔCTD GluA1 mice exhibited no memory deficits, but presented exacerbated novelty-induced hyperlocomotion and dentate gyrus granule cell (DG GC) hyperactivity, as well as other behavioral alterations. Mechanistically, we found that AMPAR EPSCs onto DG GABAergic interneurons were significantly reduced, presumably underlying, at least in part, the observed changes in neuronal activity and behavior. In summary, this study dissociates CTD-dependent from CTD-independent GluA1 functions, unveiling the GluA1 CTD as a crucial hub regulating AMPAR function in a cell type-specific manner.

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