Conformational signaling required for synaptic plasticity by the NMDA receptor complex

被引:71
|
作者
Aow, Jonathan
Dore, Kim
Malinow, Roberto [1 ]
机构
[1] Univ Calif San Diego, Dept Neurosci, Ctr Neural Circuits & Behav, San Diego, CA 92093 USA
关键词
long-term depression; LTD; NMDAR-PP1; FRET; NMDAR-CaMKII interaction; ion-flow independent; LONG-TERM DEPRESSION; PROTEIN-KINASE-II; POSTSYNAPTIC DENSITY; CAMKII; LTP; MECHANISM; PHOSPHORYLATION; POTENTIATION; ACCUMULATION; PHOSPHATASES;
D O I
10.1073/pnas.1520029112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The NMDA receptor (NMDAR) is known to transmit important information by conducting calcium ions. However, some recent studies suggest that activation of NMDARs can trigger synaptic plasticity in the absence of ion flow. Does ligand binding transmit information to signaling molecules that mediate synaptic plasticity? Using Forster resonance energy transfer (FRET) imaging of fluorescently tagged proteins expressed in neurons, conformational signaling is identified within the NMDAR complex that is essential for downstream actions. Ligand binding transiently reduces FRET between the NMDAR cytoplasmic domain (cd) and the associated protein phosphatase 1 (PP1), requiring NMDARcd movement, and persistently reduces FRET between the NMDARcd and calcium/calmodulin-dependent protein kinase II (CaMKII), a process requiring PP1 activity. These studies directly monitor agonist-driven conformational signaling at the NMDAR complex required for synaptic plasticity.
引用
收藏
页码:14711 / 14716
页数:6
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