Structural basis of long-term potentiation in single dendritic spines
Masanori Matsuzaki,
Naoki Honkura,
Graham C. R. Ellis-Davies and
Haruo Kasai ()
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Masanori Matsuzaki: National Institute for Physiological Sciences and The Graduate University of Advanced Studies (Sokendai)
Naoki Honkura: National Institute for Physiological Sciences and The Graduate University of Advanced Studies (Sokendai)
Graham C. R. Ellis-Davies: Drexel University College of Medicine
Haruo Kasai: National Institute for Physiological Sciences and The Graduate University of Advanced Studies (Sokendai)
Nature, 2004, vol. 429, issue 6993, 761-766
Abstract:
Abstract Dendritic spines of pyramidal neurons in the cerebral cortex undergo activity-dependent structural remodelling1,2,3,4,5 that has been proposed to be a cellular basis of learning and memory6. How structural remodelling supports synaptic plasticity4,5, such as long-term potentiation7, and whether such plasticity is input-specific at the level of the individual spine has remained unknown. We investigated the structural basis of long-term potentiation using two-photon photolysis of caged glutamate at single spines of hippocampal CA1 pyramidal neurons8. Here we show that repetitive quantum-like photorelease (uncaging) of glutamate induces a rapid and selective enlargement of stimulated spines that is transient in large mushroom spines but persistent in small spines. Spine enlargement is associated with an increase in AMPA-receptor-mediated currents at the stimulated synapse and is dependent on NMDA receptors, calmodulin and actin polymerization. Long-lasting spine enlargement also requires Ca2+/calmodulin-dependent protein kinase II. Our results thus indicate that spines individually follow Hebb's postulate for learning. They further suggest that small spines are preferential sites for long-term potentiation induction, whereas large spines might represent physical traces of long-term memory.
Date: 2004
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DOI: 10.1038/nature02617
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