Department of Biology, Emory University, Atlanta, GA 30322, USA.
Neuroscience. 2011 May 5;181:117-26. doi: 10.1016/j.neuroscience.2011.02.034. Epub 2011 Feb 18.
Acquiring the behavioral significance of sound has repeatedly been shown to correlate with long term changes in response properties of neurons in the adult primary auditory cortex. However, the molecular and cellular basis for such changes is still poorly understood. To address this, we have begun examining the auditory cortical expression of an activity-dependent effector immediate early gene (IEG) with documented roles in synaptic plasticity and memory consolidation in the hippocampus: Arc/Arg3.1. For initial characterization, we applied a repeated 10 min (24 h separation) sound exposure paradigm to determine the strength and consistency of sound-evoked Arc/Arg3.1 mRNA expression in the absence of explicit behavioral contingencies for the sound. We used 3D surface reconstruction methods in conjunction with fluorescent in situ hybridization (FISH) to assess the layer-specific subcellular compartmental expression of Arc/Arg3.1 mRNA. We unexpectedly found that both the intranuclear and cytoplasmic patterns of expression depended on the prior history of sound stimulation. Specifically, the percentage of neurons with expression only in the cytoplasm increased for repeated versus singular sound exposure, while intranuclear expression decreased. In contrast, the total cellular expression did not differ, consistent with prior IEG studies of primary auditory cortex. Our results were specific for cortical layers 3-6, as there was virtually no sound driven Arc/Arg3.1 mRNA in layers 1-2 immediately after stimulation. Our results are consistent with the kinetics and/or detectability of cortical subcellular Arc/Arg3.1 mRNA expression being altered by the initial exposure to the sound, suggesting exposure-induced modifications in the cytoplasmic Arc/Arg3.1 mRNA pool.
获得声音的行为意义已反复证明与成年初级听觉皮层中神经元反应特性的长期变化相关。然而,对于这种变化的分子和细胞基础仍知之甚少。为了解决这个问题,我们开始研究在海马体中具有突触可塑性和记忆巩固作用的活性依赖性效应物早期基因(IEG)在听觉皮层中的表达:Arc/Arg3.1。为了进行初步表征,我们应用了重复的 10 分钟(24 小时分离)声音暴露范式,以确定在没有声音的明确行为关联的情况下,声音诱发的 Arc/Arg3.1 mRNA 表达的强度和一致性。我们使用 3D 表面重建方法结合荧光原位杂交(FISH)来评估 Arc/Arg3.1 mRNA 的亚细胞层特异性表达。我们出人意料地发现,核内和细胞质表达模式都依赖于先前的声音刺激史。具体来说,与单次声音暴露相比,重复声音暴露时仅在细胞质中表达的神经元比例增加,而核内表达减少。相比之下,总细胞表达没有差异,与先前的初级听觉皮层 IEG 研究一致。我们的结果是针对皮质 3-6 层的,因为在刺激后几乎没有声音驱动的 Arc/Arg3.1 mRNA 在 1-2 层。我们的结果与皮质亚细胞 Arc/Arg3.1 mRNA 表达的动力学和/或可检测性被初始暴露于声音改变一致,表明暴露诱导的细胞质 Arc/Arg3.1 mRNA 库的修饰。