GluR7 is an essential subunit of presynaptic kainate autoreceptors at hippocampal mossy fiber synapses

被引:111
|
作者
Pinheiro, Paulo S.
Perrais, David
Coussen, Francois
Barhanin, Jacques
Bettler, Bernhard
Mann, Jeffrey R.
Malva, Joao O.
Heinemar, Stephen F.
Mulle, Christophe [1 ]
机构
[1] Univ Bordeaux 1, Bordeaux Neurosci Inst, Ctr Natl Rech Sci, LAb Physiol Cellular Synapse, F-33077 Bordeaux, France
[2] Univ Coimbra, Fac Med, Inst Biochem, Ctr Neurosci & Cell Biol Coimbra, P-3004 Coimbra, Portugal
[3] Salk Inst Biol Studies, Mol Neurobiol Lab, La Jolla, CA 92037 USA
[4] City Hope Natl Med Ctr, Beckman Res Inst, Div Biol, Duarte, CA 91010 USA
关键词
kainate receptors; presynaptic glutamate receptors; short-term plasticity; synaptic plasticity;
D O I
10.1073/pnas.0608891104
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
Presynaptic ionotropic glutamate receptors are emerging as key players in the regulation of synaptic transmission. Here we identify GluR7 a kainate receptor (KAR) subunit with no known function in the brain, as an essential subunit of presynaptic autoreceptors that facilitate hippocampal mossy fiber synaptic transmission. GluR7-1mice display markedly reduced short- and long-term synaptic potentiation. Our data suggest that presynaptic KARs are GluR6/ GluR7 heteromers that coassemble and are localized within synapses. We show that recombinant GluR6/GluR7 KARs exhibit low sensitivity to glutamate, and we provide evidence that presynaptic KARs at mossy fiber synapses are likely activated by high concentrations of glutamate. Overall, from our data, we propose a model whereby presynaptic KARs are localized in the presynaptic active zone close to release sites, display low affinity for glutamate, are likely Ca2+-permeable, are activated by single release events, and operate within a short time window to facilitate the subsequent release of glutamate.
引用
收藏
页码:12181 / 12186
页数:6
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