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Sox11 是一种活性调节基因,在普遍的神经激活时具有齿状回特异性表达。

Sox11 is an Activity-Regulated Gene with Dentate-Gyrus-Specific Expression Upon General Neural Activation.

机构信息

Institute of Biochemistry, Emil Fischer Center, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.

Department of Biology, Animal Physiology, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany.

出版信息

Cereb Cortex. 2020 May 18;30(6):3731-3743. doi: 10.1093/cercor/bhz338.

DOI:10.1093/cercor/bhz338
PMID:32080705
Abstract

Neuronal activity initiates transcriptional programs that shape long-term changes in plasticity. Although neuron subtypes differ in their plasticity response, most activity-dependent transcription factors (TFs) are broadly expressed across neuron subtypes and brain regions. Thus, how region- and neuronal subtype-specific plasticity are established on the transcriptional level remains poorly understood. We report that in young adult (i.e., 6-8 weeks old) mice, the developmental TF SOX11 is induced in neurons within 6 h either by electroconvulsive stimulation or by exploration of a novel environment. Strikingly, SOX11 induction was restricted to the dentate gyrus (DG) of the hippocampus. In the novel environment paradigm, SOX11 was observed in a subset of c-FOS expressing neurons (ca. 15%); whereas around 75% of SOX11+ DG granule neurons were c-FOS+, indicating that SOX11 was induced in an activity-dependent fashion in a subset of neurons. Environmental enrichment or virus-mediated overexpression of SOX11 enhanced the excitability of DG granule cells and downregulated the expression of different potassium channel subunits, whereas conditional Sox11/4 knock-out mice presented the opposite phenotype. We propose that Sox11 is regulated in an activity-dependent fashion, which is specific to the DG, and speculate that activity-dependent Sox11 expression may participate in the modulation of DG neuron plasticity.

摘要

神经元活动启动了可塑造长期可塑性变化的转录程序。尽管神经元亚型在其可塑性反应上存在差异,但大多数依赖于活动的转录因子(TFs)在神经元亚型和脑区中广泛表达。因此,区域和神经元亚型特异性可塑性如何在转录水平上建立仍知之甚少。我们报告说,在年轻成年(即 6-8 周龄)小鼠中,发育性 TF SOX11 在电惊厥刺激或探索新环境后 6 小时内被诱导到神经元中。引人注目的是,SOX11 的诱导仅限于海马的齿状回(DG)。在新环境范式中,SOX11 观察到在一小部分 c-FOS 表达神经元中(约 15%);而大约 75%的 SOX11+DG 颗粒神经元为 c-FOS+,表明 SOX11 以依赖于活动的方式在一小部分神经元中被诱导。环境丰富或病毒介导的 SOX11 过表达增强了 DG 颗粒细胞的兴奋性,并下调了不同钾通道亚基的表达,而条件性 Sox11/4 敲除小鼠则表现出相反的表型。我们提出 Sox11 以依赖于活动的方式被调节,这种方式是 DG 特异性的,并推测依赖于活动的 Sox11 表达可能参与了 DG 神经元可塑性的调节。

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