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在小鼠颞叶联合皮层中恐惧条件作用激活的神经团进行 RNA 测序。

RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex.

机构信息

Harvard Medical School, Genetics Department, 77 Ave Louis Pasteur NRB Room 356, Boston, Massachusetts 02115, USA.

University of California at Los Angeles, David Geffen School of Medicine, Department of Neurology, 710 Westwood Plaza, Los Angeles, California 90095, USA.

出版信息

Sci Rep. 2016 Aug 25;6:31753. doi: 10.1038/srep31753.

Abstract

The stable formation of remote fear memories is thought to require neuronal gene induction in cortical ensembles that are activated during learning. However, the set of genes expressed specifically in these activated ensembles is not known; knowledge of such transcriptional profiles may offer insights into the molecular program underlying stable memory formation. Here we use RNA-Seq to identify genes whose expression is enriched in activated cortical ensembles labeled during associative fear learning. We first establish that mouse temporal association cortex (TeA) is required for remote recall of auditory fear memories. We then perform RNA-Seq in TeA neurons that are labeled by the activity reporter Arc-dVenus during learning. We identify 944 genes with enriched expression in Arc-dVenus+ neurons. These genes include markers of L2/3, L5b, and L6 excitatory neurons but not glial or inhibitory markers, confirming Arc-dVenus to be an excitatory neuron-specific but non-layer-specific activity reporter. Cross comparisons to other transcriptional profiles show that 125 of the enriched genes are also activity-regulated in vitro or induced by visual stimulus in the visual cortex, suggesting that they may be induced generally in the cortex in an experience-dependent fashion. Prominent among the enriched genes are those encoding potassium channels that down-regulate neuronal activity, suggesting the possibility that part of the molecular program induced by fear conditioning may initiate homeostatic plasticity.

摘要

远程恐惧记忆的稳定形成被认为需要在学习过程中激活的皮质集合体中的神经元基因诱导。然而,在这些激活的集合体中特异性表达的基因集尚不清楚;对这些转录谱的了解可能为稳定记忆形成的分子程序提供深入的见解。在这里,我们使用 RNA-Seq 来鉴定在关联性恐惧学习期间标记的激活皮质集合体中表达丰富的基因。我们首先确定,在听觉恐惧记忆的远程回忆中,需要小鼠时间关联皮层 (TeA)。然后,我们在学习过程中通过活性报告基因 Arc-dVenus 标记的 TeA 神经元中进行 RNA-Seq。我们鉴定了在 Arc-dVenus+神经元中表达丰富的 944 个基因。这些基因包括 L2/3、L5b 和 L6 兴奋性神经元的标志物,但不包括神经胶质或抑制性标志物,这证实 Arc-dVenus 是一种兴奋性神经元特异性但非层特异性的活性报告基因。与其他转录谱的交叉比较表明,125 个丰富的基因在体外也受活性调节,或者在视觉皮层中受视觉刺激诱导,这表明它们可能以经验依赖性的方式在皮层中普遍诱导。在丰富的基因中,编码钾通道的基因尤为突出,这些钾通道可下调神经元活性,这表明恐惧条件作用诱导的分子程序的一部分可能会引发同源性可塑性。

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