Copine-6 is a Ca2+ sensor for activity-induced AMPA receptor exocytosis

Abstract

The recruitment of synaptic α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors underlies the strengthening of neuronal connectivity during learning and memory. This process is triggered by N-methyl-D-aspartate (NMDA) receptor-dependent postsynaptic Ca²⁺ influx. Synaptotagmin (Syt)-1 and -7 have been proposed as Ca²⁺ sensors for AMPA receptor exocytosis but are functionally redundant. Here, we identify a cytosolic C2 domain-containing Ca²⁺-binding protein, Copine-6, that forms a complex with AMPA receptors. Loss of Copine-6 expression impairs activity-induced exocytosis of AMPA receptors in primary neurons, which is rescued by wild-type Copine-6 but not Ca²⁺-binding mutants. In contrast, Copine-6 loss of function does not affect steady-state expression or tetrodotoxin-induced synaptic upscaling of surface AMPA receptors. Loss of Syt-1/Syt-7 significantly reduces Copine-6 protein expression. Interestingly, overexpression of wild-type Copine-6, but not the Ca²⁺-binding mutants, restores activity-dependent exocytosis of AMPA receptors in Syt-1/Syt-7 double-knockdown neurons. We conclude that Copine-6 is a postsynaptic Ca²⁺ sensor that mediates AMPA receptor exocytosis during synaptic potentiation.

Keywords: AMPA receptors; C2 domain; CP: Cell biology; CP: Neuroscience; Copine; calcium sensor; dendrite; endosomes; exocytosis; glutamate; synaptic potentiation; trafficking.