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Publication : Barrel cortex critical period plasticity is independent of changes in NMDA receptor subunit composition.

First Author  Lu HC Year  2001
Journal  Neuron Volume  32
Issue  4 Pages  619-34
PubMed ID  11719203 Mgi Jnum  J:107683
Mgi Id  MGI:3621670 Doi  10.1016/s0896-6273(01)00501-3
Citation  Lu HC, et al. (2001) Barrel cortex critical period plasticity is independent of changes in NMDA receptor subunit composition. Neuron 32(4):619-34
abstractText  The regulation of NMDA receptor (NMDAR) subunit composition and expression during development is thought to control the process of thalamocortical afferent innervation, segregation, and plasticity. Thalamocortical synaptic plasticity in the mouse is dependent on NMDARs containing the NR2B subunit, which are the dominant form during the 'critical period' window for plasticity. Near the end of the critical period there is a gradual increase in the contribution of NR2A subunits that happens in parallel to changes in NMDAR-mediated current kinetics. However, no extension of the critical period occurs in NR2A knockout mice, despite the fact that NMDA subunit composition and current kinetics remain immature past the end of the critical period. These data suggest that regulation of NMDAR subunit composition is not essential for closing the critical period plasticity window in mouse somatosensory barrel cortex.
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