Shimshek Derya R, Bus Thorsten, Schupp Bettina, Jensen Vidar, Marx Verena, Layer Liliana E, Köhr Georg, Sprengel Rolf
Department of Molecular Neurobiology, Max Planck Institute for Medical ResearchHeidelberg, Germany.
Research Group of the Max Planck Institute for Medical Research, Institute for Anatomy and Cell Biology, Heidelberg UniversityHeidelberg, Germany.
Front Mol Neurosci. 2017 Jul 4;10:214. doi: 10.3389/fnmol.2017.00214. eCollection 2017.
Spatial working memory (SWM) and the classical, tetanus-induced long-term potentiation (LTP) at hippocampal CA3/CA1 synapses are dependent on L-α-amino-3-hydroxy-5-methylisoxazole-4-propionate receptors (AMPARs) containing GluA1 subunits as demonstrated by knockout mice lacking GluA1. In GluA1 knockout mice LTP and SWM deficits could be partially recovered by transgenic re-installation of full-length GluA1 in principle forebrain neurons. Here we partially restored hippocampal LTP in GluA1-deficient mice by forebrain-specific depletion of the GluA2 gene, by the activation of a hypomorphic GluA2(Q) allele and by transgenic expression of PDZ-site truncated GFP-GluA1(TG). In none of these three mouse lines, the partial LTP recovery improved the SWM performance of GluA1-deficient mice suggesting a specific function of intact GluA1/2 receptors and the GluA1 intracellular carboxyl-terminus in SWM and its associated behavior.
空间工作记忆(SWM)以及海马体CA3/CA1突触处经典的、破伤风毒素诱导的长时程增强(LTP)依赖于含有GluA1亚基的α-氨基-3-羟基-5-甲基异恶唑-4-丙酸受体(AMPARs),这一点已被缺乏GluA1的基因敲除小鼠所证实。在GluA1基因敲除小鼠中,通过在前脑神经元中转基因重新安装全长GluA1,LTP和SWM缺陷可部分恢复。在此,我们通过前脑特异性敲除GluA2基因、激活低表达的GluA2(Q)等位基因以及转基因表达PDZ位点截短的GFP-GluA1(TG),部分恢复了GluA1缺陷小鼠的海马体LTP。在这三种小鼠品系中,LTP的部分恢复均未改善GluA1缺陷小鼠的SWM表现,这表明完整的GluA1/2受体以及GluA1细胞内羧基末端在SWM及其相关行为中具有特定功能。