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经典条件反射中的两阶段 AMPA 受体转运和谷氨酸受体亚基 4(tGluA4)翻转剪接变体的选择性作用。

Two-stage AMPA receptor trafficking in classical conditioning and selective role for glutamate receptor subunit 4 (tGluA4) flop splice variant.

机构信息

Neuroscience Group, Division of Basic Biomedical Sciences, University of South Dakota, Sanford School of Medicine, Vermillion, SD 57069, USA.

出版信息

J Neurophysiol. 2012 Jul;108(1):101-11. doi: 10.1152/jn.01097.2011. Epub 2012 Apr 4.

Abstract

Previously, we proposed a two-stage model for an in vitro neural correlate of eyeblink classical conditioning involving the initial synaptic incorporation of glutamate receptor A1 (GluA1)-containing α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid type receptors (AMPARs) followed by delivery of GluA4-containing AMPARs that support acquisition of conditioned responses. To test specific elements of our model for conditioning, selective knockdown of GluA4 AMPAR subunits was used using small-interfering RNAs (siRNAs). Recently, we sequenced and characterized the GluA4 subunit and its splice variants from pond turtles, Trachemys scripta elegans (tGluA4). Analysis of the relative abundance of mRNA expression by real-time RT-PCR showed that the flip/flop variants of tGluA4, tGluA4c, and a novel truncated variant tGluA4trc1 are major isoforms in the turtle brain. Here, transfection of in vitro brain stem preparations with anti-tGluA4 siRNA suppressed conditioning, tGluA4 mRNA and protein expression, and synaptic delivery of tGluA4-containing AMPARs but not tGluA1 subunits. Significantly, transfection of abducens motor neurons by nerve injections of tGluA4 flop rescue plasmid prior to anti-tGluA4 siRNA application restored conditioning and synaptic incorporation of tGluA4-containing AMPARs. In contrast, treatment with rescue plasmids for tGluA4 flip or tGluA4trc1 failed to rescue conditioning. Finally, treatment with a siRNA directed against GluA1 subunits inhibited conditioning and synaptic delivery of tGluA1-containing AMPARs and importantly, those containing tGluA4. These data strongly support our two-stage model of conditioning and our hypothesis that synaptic incorporation of tGluA4-containing AMPARs underlies the acquisition of in vitro classical conditioning. Furthermore, they suggest that tGluA4 flop may have a critical role in conditioning mechanisms compared with the other tGluA4 splice variants.

摘要

先前,我们提出了一个两阶段模型,用于体外眨眼经典条件反射的神经相关研究,该模型涉及谷氨酸受体 A1 (GluA1) 包含的 α-氨基-3-羟基-5-甲基异恶唑-4-丙酸型受体 (AMPAR) 的初始突触整合,随后是支持条件反应获得的 GluA4 包含的 AMPAR 的传递。为了测试我们的条件反射模型的特定元素,使用小干扰 RNA (siRNA) 对 GluA4 AMPAR 亚基进行选择性敲低。最近,我们对池塘龟(Trachemys scripta elegans)的 GluA4 亚基及其剪接变体进行了测序和特征分析。实时 RT-PCR 分析相对 mRNA 表达丰度表明,tGluA4 的翻转变体 tGluA4c 和一种新型截断变体 tGluA4trc1 是龟脑中的主要同工型。在这里,用抗 tGluA4 siRNA 转染体外脑干制备物可抑制条件反射、tGluA4 mRNA 和蛋白表达以及包含 tGluA4 的 AMPAR 的突触传递,但不抑制 tGluA1 亚基。重要的是,在应用抗 tGluA4 siRNA 之前,通过神经注射 tGluA4 翻转挽救质粒转染外展运动神经元可恢复条件反射和包含 tGluA4 的 AMPAR 的突触整合。相比之下,用 tGluA4 翻转或 tGluA4trc1 的挽救质粒处理未能挽救条件反射。最后,用针对 GluA1 亚基的 siRNA 处理抑制了条件反射和包含 tGluA1 的 AMPAR 的突触传递,重要的是,还抑制了包含 tGluA4 的 AMPAR 的突触传递。这些数据强烈支持我们的条件反射两阶段模型以及我们的假设,即包含 tGluA4 的 AMPAR 的突触整合是体外经典条件反射获得的基础。此外,它们表明与其他 tGluA4 剪接变体相比,tGluA4 翻转可能在调节机制中发挥关键作用。

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