Dynamic control of NMDA receptor Ca²⁺ permeability by endogenous and synthetic modulators.

Abstract

NMDA receptors are principal sources of postsynaptic Ca²⁺ in central neurons. It is widely assumed that the content of Ca²⁺ in the glutamate-elicited ionic flux is determined by the molecular composition of the NMDA receptors, whose expression varies developmentally and across brain regions and can change on a scale of minutes to hours. Here, we report that rather than being a fixed property of a given receptor assembly, the amount of Ca²⁺ in the NMDA receptor current can fluctuate in real time over a wide dynamic range in response to endogenous and synthetic allosteric modulators. We identify the extracellular N-terminal domain of the receptor as a structural modulator of its Ca²⁺ permeability and demonstrate that the mechanism involves changes in the receptor's unitary Ca²⁺ conductance. These results reveal an unsuspected lever controlling the NMDA receptor-mediated Ca²⁺ transients and, implicitly, the many physiological and pathological processes influenced by these currents.