The N-methyl-D-aspartate (NMDA) glutamate receptor (NMDAR), long implicated in developmental plasticity, shows decay time kinetics that shorten postnatally as NR2A subunits are added to the receptor. Neither the mechanism nor immediate effect of this change is known. We studied developing NMDAR currents by using visual neurons in slices from NR2A knockout (NR2AKO) and WT mice. Both strains show increased dendritic levels of synaptic density scaffolding protein PSD-95 with age. Dendritic levels of NR2A increased at the same time in WT and immunoprecipitated with PSD-95. PSD-95͞NMDAR binding was significantly decreased in the NR2AKO. Moreover, NMDAR miniature currents (minis) were lost and rise times of NMDAR evoked currents increased in mutant mice. Age-matched WT cells showed NR2A-rich receptors predominating in minis, yet slow NR2B mediated currents persisted in evoked currents. Disrupting photoreceptor activation of retinal ganglion cells eliminated increases in PSD-95 and NR2A in superior collicular dendrites of WT mice and slowed the loss of miniature NMDAR currents in NR2AKOs. These data demonstrate that NMDARs that respond to single quantal events mature faster during development by expressing the NR2A subunit earlier than NMDARs that respond to evoked release. We hypothesize that NR2A-rich NMDARs may be localized to the center of developing synapses by an activity-dependent process that involves the targeting of PSD-95 to the postsynaptic density. Neonatal receptors become restricted to perisynpatic or extrasynaptic sites, where they participate primarily in evoked currents.
I n visual pathways, N-methyl-D-aspartate (NMDA) receptors(NMDARs) contain NR1 (GluR 1) plus varying proportions of NR2A (GluR 1) and NR2B (GluR 2) subunits (1, 2). The decay times of evoked NMDAR currents (NMDARcs) become faster during development as NR2A is incorporated (3-6). Reducing visual activity, delays synaptic refinement in the visual cortex (VC) (7,8), delays the shortening of NMDRc decay time (9) and up-regulation of NR2A (10). Furthermore dark-reared rats rapidly up-regulate NR2A at cortical synapses upon light exposure, whereas rats placed in darkness down-regulate NR2A in dendrites over several days (11,12). The mechanism of this rapid activity-dependent trafficking is unknown, but related work in our laboratory suggests that scaffolding of the NMDAR by PSD-95 may be involved.
MethodsAnimals. All surgical procedures were compliant with the Massachusetts Institute of Technology Committee on Animal Care (CAC) animal protocol review. WT C57BL͞6 mice and NR2AKO mice (13) with a C57BL͞6 background were used in all experiments. All animals were killed before eye opening on postnatal day 13 (P13).Surgery. Preparation of Elvax plastic (DuPont) for drug delivery in the eye was carried out as in ref. 14. Glutamate antagonists were dissolved in DMSO and Elvax [MK801 final concentration ϭ 6 mM, estimated active concentration in eye ϭ 200 M and 2,3-dihydroxy-6-nitro-7-sulfamoylbenzo[f]quinoxaline (NBQX) final concentration ϭ 600 M, ...