Marrone Diano F, Schaner Michael J, McNaughton Bruce L, Worley Paul F, Barnes Carol A
Division of Neural Systems, Memory, and Aging, Arizona Research Laboratories, Tucson, Arizona 85724, USA.
J Neurosci. 2008 Jan 30;28(5):1030-3. doi: 10.1523/JNEUROSCI.4235-07.2008.
Immediate-early genes (IEGs) are tightly coupled to cellular activity and play a critical role in regulating synaptic plasticity. While encoding spatial experience, hippocampal principal cells express IEGs in a behaviorally dependent and cell-specific manner. This expression can be detected through the use of cellular compartment analysis of temporal activity by fluorescence in situ hybridization to generate estimates of cellular activity that match direct neuronal recording under comparable conditions. During rest, IEG expression continues to occur in a small number of cells, and the role of this basal expression is unknown. Imaging IEGs expressed during exploration and adjacent rest periods reveals that "constitutive" IEG expression during rest is not random. Rather, consistent with proposed memory consolidation mechanisms, it recapitulates a subset of the pattern generated by recent experience.
即早基因(IEGs)与细胞活动紧密相关,在调节突触可塑性方面发挥着关键作用。在编码空间经验时,海马体主细胞以行为依赖和细胞特异性的方式表达即早基因。通过荧光原位杂交对时间活动进行细胞区室分析,可以检测到这种表达,从而生成与可比条件下直接神经元记录相匹配的细胞活动估计值。在休息期间,即早基因表达仍会在少数细胞中发生,而这种基础表达的作用尚不清楚。对探索期间和相邻休息期表达的即早基因进行成像显示,休息期间的“组成性”即早基因表达并非随机的。相反,与提出的记忆巩固机制一致,它重现了近期经验产生的模式的一个子集。