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转录因子与内侧神经节隆起衍生的皮质中间神经元迁移的调控。

Transcription Factors and Regulate Medial Ganglionic Eminence-Derived Cortical Interneuron Migration.

作者信息

Tao Guangxu, Li Zhenmeiyu, Wen Yan, Song Xiaolei, Wei Song, Du Heng, Yang Zhengang, Xu Zhejun, You Yan

机构信息

State Key Laboratory of Medical Neurobiology, MOE Frontier Research Center for Brain Science, Department of Neurology, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Front Mol Neurosci. 2019 Apr 2;12:75. doi: 10.3389/fnmol.2019.00075. eCollection 2019.

Abstract

Cortical interneurons are derived from the subpallium and reach the developing cortex through long tangential migration. Mature cortical interneurons are characterized by remarkable morphological, molecular, and functional diversity. The calcium-binding protein parvalbumin (PV) and neuropeptide somatostatin (SST) identify most medial ganglionic eminence (MGE)-derived cortical interneurons. Previously, we demonstrated that plays a curial transcriptional role in regulating MGE-derived cortical interneuron development. Here, we show that SP8 protein is weekly expressed in the MGE mantle zone of wild type mice but upregulated in null mutants. PV cortical interneurons were severely lost in double conditional knockouts due to defects in tangential migration compared with single mutants, suggesting that coordinately regulate PV cortical interneuron development. We provide evidence that activity is required for normal MGE-derived cortical interneuron migration, at least in part, through regulating the expression of , , and .

摘要

皮质中间神经元起源于皮质下神经节,通过长距离的切向迁移到达发育中的皮质。成熟的皮质中间神经元具有显著的形态、分子和功能多样性。钙结合蛋白小白蛋白(PV)和神经肽生长抑素(SST)可识别大多数源自内侧神经节隆起(MGE)的皮质中间神经元。此前,我们证明了 在调节源自MGE的皮质中间神经元发育中发挥关键的转录作用。在此,我们表明SP8蛋白在野生型小鼠的MGE套层区表达较弱,但在 基因敲除突变体中上调。与 单基因敲除突变体相比,由于切向迁移缺陷,PV皮质中间神经元在 双条件敲除小鼠中严重缺失,这表明 协同调节PV皮质中间神经元的发育。我们提供的证据表明, 活性对于源自MGE的皮质中间神经元的正常迁移是必需的,至少部分是通过调节 、 和 的表达来实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262b/6454190/4c9a96339799/fnmol-12-00075-g0001.jpg

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