Pinheiro Paulo S, Perrais David, Coussen Françoise, Barhanin Jacques, Bettler Bernhard, Mann Jeffrey R, Malva João O, Heinemann Stephen F, Mulle Christophe
Laboratoire Physiologie Cellulaire de la Synapse, Centre National de la Recherche Scientifique, Bordeaux Neuroscience Institute, University of Bordeaux, 33077 Bordeaux Cedex, France.
Proc Natl Acad Sci U S A. 2007 Jul 17;104(29):12181-6. doi: 10.1073/pnas.0608891104. Epub 2007 Jul 9.
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(-/-) mice 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 Ca(2+)-permeable, are activated by single release events, and operate within a short time window to facilitate the subsequent release of glutamate.
突触前离子型谷氨酸受体正逐渐成为调节突触传递的关键因素。在此,我们确定了GluR7,一种在大脑中尚无已知功能的海人藻酸受体(KAR)亚基,它是突触前自身受体的一个重要亚基,有助于海马苔藓纤维突触传递。GluR7基因敲除小鼠表现出明显降低的短期和长期突触增强。我们的数据表明,突触前KARs是由GluR6/GluR7共同组装并定位于突触内的异聚体。我们发现重组GluR6/GluR7 KARs对谷氨酸的敏感性较低,并且我们提供证据表明苔藓纤维突触处的突触前KARs可能由高浓度谷氨酸激活。总体而言,根据我们的数据,我们提出了一个模型,即突触前KARs定位于靠近释放位点的突触前活性区,对谷氨酸具有低亲和力,可能是钙通透性的,由单个释放事件激活,并在短时间窗口内发挥作用以促进随后谷氨酸的释放。