Calmodulin Mediates Calcium-Dependent Inactivation of N-Methyl-D-Aspartate Receptors

Abstract

Ca²⁺ influx through N-methyl-D-aspartate (NMDA) receptors activates signal transduction pathways critical for many forms of synaptic plasticity in the brain. NMDA receptor–mediated Ca²⁺ influx also downregulates the gating of NMDA channels through a process called Ca²⁺-dependent inactivation (CDI). Recent studies have demonstrated that the calcium binding protein calmodulin directly interacts with NMDA receptors, suggesting that calmodulin may play a role in CDI. We report here that the mutation of a specific calmodulin binding site in the C0 region of the NR1 subunit of the NMDA receptor blocks CDI. Moreover, intracellular infusion of a calmodulin inhibitory peptide markedly reduces CDI of both recombinant and neuronal NMDA receptors. Furthermore, this inactivating effect of calmodulin can be prevented by coexpressing a region of the cytoskeletal protein α-actinin2 known to interact with the C0 region of NR1. Taken together, these results demonstrate that the binding of Ca²⁺/calmodulin to NR1 mediates CDI of the NMDA receptor and suggest that inactivation occurs via Ca²⁺/calmodulin-dependent release of the receptor complex from the neuronal cytoskeleton.