Abstract
Specific patterns of neuronal firing induce changes in synaptic strength that may contribute to learning and memory. If the postsynaptic NMDA (N-methyl-D-aspartate) receptors are blocked, long-term potentiation (LTP) and long-term depression (LTD) of synaptic transmission and the learning of spatial information are prevented. The NMDA receptor can bind a protein known as postsynaptic density-95 (PSD-95), which may regulate the localization of and/or signalling by the receptor. In mutant mice lacking PSD-95, the frequency function of NMDA-dependent LTP and LTD is shifted to produce strikingly enhanced LTP at different frequencies of synaptic stimulation. In keeping with neural-network models that incorporate bidirectional learning rules, this frequency shift is accompanied by severely impaired spatial learning. Synaptic NMDA-receptor currents, subunit expression, localization and synaptic morphology are all unaffected in the mutant mice. PSD-95 thus appears to be important in coupling the NMDA receptor to pathways that control bidirectional synaptic plasticity and learning.
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Acknowledgements
We thank A. J. H. Smith for advice and for the 129 genomic library, J. Ure for embryo injection, L. Anderson and J. Young for mouse care, W. Janssen for technical assistance, F. Johnston and G.Brown for photography, and R. Ellaway for illustrations. This work was supported by the Fyssen Foundation (M.M.) and the BBSRC (M.M., M.D. and P.C.), by grants from the NIH and the Charles A. Dana Foundation (J.H.M. and Y.H.), the Esther A. and Joseph Klingenstein Fund and the Pew Charitable Trusts (T.J.O.), a grant from the National Institute of Mental Health (T.J.O.), and the Wellcome Trust (L.C.W. and S.G.N.G.).
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Migaud, M., Charlesworth, P., Dempster, M. et al. Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein. Nature 396, 433–439 (1998). https://doi.org/10.1038/24790
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DOI: https://doi.org/10.1038/24790
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