Barberis Andrea, Sachidhanandam Shankar, Mulle Christophe
Laboratoire Physiologie Cellulaire de la Synapse, Centre National de la Recherche Scientifique Unité Mixte de Recherche 5091, Bordeaux Neuroscience Institute, University of Bordeaux 2, 33077 Bordeaux, France.
J Neurosci. 2008 Jun 18;28(25):6402-6. doi: 10.1523/JNEUROSCI.1204-08.2008.
Kainate receptors (KARs) are ionotropic glutamate receptors contributing to EPSCs with a slow-decaying component that is likely essential for synaptic integration. The slow kinetics of KAR-EPSCs markedly contrasts with the fast kinetics reported for recombinant KARs expressed in heterologous systems, for reasons that remain unexplained. Here we have studied the properties of recombinant heteromeric GluR6/KA2 receptors, which compose synaptic KARs. We report that, in response to brief glutamate applications, currents mediated by recombinant GluR6/KA2 receptors, but not GluR6 receptors, decay with a time course similar to KAR-EPSCs. Model simulations suggest that, after brief agonist exposures, GluR6/KA2 currents undergo slow deactivation caused by the stabilization of partially bound open states. We propose, therefore, that the GluR6/KA2 gating features could contribute to the slow KAR-EPSC decay kinetics.
海人藻酸受体(KARs)是离子型谷氨酸受体,对具有缓慢衰减成分的兴奋性突触后电流(EPSCs)有贡献,该成分可能对突触整合至关重要。KAR-EPSCs的缓慢动力学与在异源系统中表达的重组KARs所报道的快速动力学形成显著对比,其原因尚不清楚。在这里,我们研究了构成突触KARs的重组异聚体GluR6/KA2受体的特性。我们报告称,响应短暂的谷氨酸应用,由重组GluR6/KA2受体介导的电流,而不是GluR6受体介导的电流,其衰减时间进程与KAR-EPSCs相似。模型模拟表明,在短暂的激动剂暴露后,GluR6/KA2电流会因部分结合的开放状态的稳定而经历缓慢失活。因此,我们提出,GluR6/KA2的门控特性可能有助于KAR-EPSC的缓慢衰减动力学。