Interactions of Calmodulin and α-Actinin with the NR1 Subunit Modulate Ca²⁺-Dependent Inactivation of NMDA Receptors

Abstract

Glutamate receptors are associated with various regulatory and cytoskeletal proteins. However, an understanding of the functional significance of these interactions is still rudimentary. Studies in hippocampal neurons suggest that such interactions may be involved in calcium-induced reduction in the open probability of NMDA receptors (inactivation). Thus we examined the role of the intracellular domains of the NR1 subunit and two of its binding partners, calmodulin and alpha-actinin, on this process using NR1/NR2A heteromers expressed in human embryonic kidney (HEK) 293 cells. The presence of the first 30 residues of the intracellular C terminus of NR1 (C0 domain) was required for inactivation. Mutations in the last five residues of C0 reduced inactivation and produced parallel shifts in binding of alpha-actinin and Ca2+/calmodulin to the respective C0-derived peptides. Although calmodulin reduced channel activity in excised patches, calmodulin inhibitors did not block inactivation in whole-cell recording, suggesting that inactivation in the intact cell is more complex than binding of calmodulin to C0. Overexpression of putative Ca2+-insensitive, but not Ca2+-sensitive, forms of alpha-actinin reduced inactivation, an effect that was overcome by inclusion of calmodulin in the whole-cell pipette. The C0 domain also directly affects channel gating because NR1 subunits with truncated C0 domains that lacked calmodulin or alpha-actinin binding sites had a low open probability. We propose that inactivation can occur after C0 dissociates from alpha-actinin by two distinct but converging calcium-dependent processes: competitive displacement of alpha-actinin by calmodulin and reduction in the affinity of alpha-actinin for C0 after binding of calcium to alpha-actinin.

Organization of Ionotropic Glutamate Receptors at Dendrodendritic Synapses in the Rat Olfactory Bulb

“…An alternative explanation is that the C-terminal domain has different configurations, which depend on its dynamic interactions with the cytoskeleton. In support of this intriguing possibility, it has been shown that the binding of NR1 to ␣-actinin is displaced by calmodulin (Wyszynski et al, 1997), a process that might explain the calcium-dependent inactivation of NMDA receptors (Ehlers et al, 1996;Zhang et al, 1998;Krupp et al, 1999).…”

Dendritic spine actin cytoskeleton in autism spectrum disorder

“…Dimer formation is required for its normal function as a cross-linker of the actin cytoskeleton 111 (Figure 2). In addition to binding to actin filaments, actinins interact with membrane receptors [112][113][114][115] However, the expression and function of Villin 1 in neurons is currently unknown.…”

Zinc reverses glycine-dependent inactivation of NMDARs in cultured rat hippocampal neurons

“…Many mechanisms have been proposed to account for the mediation of the inactivation of NMDARs, including glycine-dependent desensitization, glycine-independent desensitization [5,6], Ca 2+ -dependent inactivation [7][8][9] and surface membrane receptors internalization [10]. Activation of NMDARs that have been pre-equilibrated with glycine produces a peak current, which decays or desensitizes to a steady-state level at high concentrations of NMDA.…”