Excitation control: balancing PSD-95 function at the synapse

Dove Keith

Frontiers in Molecular Neuroscience · 2008 · 212 citations · 169 references

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Concepts

TL;DR

Neuronal excitability governs circuit activity and is regulated by synaptic molecules, receptor abundance, and signaling proteins at individual synapses. This review aims to elucidate how PSD‑95 targeting mechanisms influence synaptic protein clustering and excitation–inhibition balance. It examines the molecular pathways that direct PSD‑95 to synapses and regulate the retention of neurotransmitter receptors, adhesion molecules, ion channels, cytoskeletal elements, and signaling proteins. PSD‑95 is essential for clustering neurotransmitter receptors, adhesion molecules, ion channels, cytoskeletal elements, and signaling proteins at glutamatergic postsynaptic sites.

Abstract

Excitability of individual neurons dictates the overall excitation in specific brain circuits. This process is thought to be regulated by molecules that regulate synapse number, morphology and strength. Neuronal excitation is also influenced by the amounts of neurotransmitter receptors and signaling molecules retained at particular synaptic sites. Recent studies revealed a key role for PSD-95, a scaffolding molecule enriched at glutamatergic synapses, in modulation of clustering of several neurotransmitter receptors, adhesion molecules, ion channels, cytoskeletal elements and signaling molecules at postsynaptic sites. In this review we will highlight mechanisms that control targeting of PSD-95 at the synapse, and discuss how this molecule influences the retention and clustering of diverse synaptic proteins to regulate synaptic structure and strength. We will also discuss how PSD-95 may maintain a balance between excitation and inhibition in the brain and how alterations in this balance may contribute to neuropsychiatric disorders.

References

169