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核因子 kappa B 信号通路启动神经干细胞的早期分化。

Nuclear factor kappa B signaling initiates early differentiation of neural stem cells.

机构信息

Laboratory of Stem Cell Biology, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, People's Republic of China.

出版信息

Stem Cells. 2012 Mar;30(3):510-24. doi: 10.1002/stem.1006.

Abstract

Inflammatory mediators, many of which activate the signaling of nuclear factor kappa B (NFκB), have received increasing attention in the field of neurogenesis. NFκB signaling regulates neurite outgrowth and neural plasticity as well as the proliferation/apoptosis and terminal differentiation of neural stem cells (NSCs). Early neurogenesis from NSCs produces identical progeny through symmetric division and committed daughter cells through asymmetric division. Here, we show that NFκB signaling is required for NSC initial differentiation. The canonical IKKβ/IκBα/p65 pathway is activated during the initial stages of neural differentiation induced by treatment with TNFα or withdrawal of epidermal growth factor/basic fibroblast growth factor. NSC-specific inhibition of NFκB in transgenic mice causes an accumulation of Nestin(+) /Sox2(+) /glial fibrillary acidic protein(+) NSCs. Inhibition of NFκB signaling in vitro blocks differentiation and asymmetric division and maintains NSCs in an undifferentiated state. The induction of initial differentiation and asymmetry by NFκB signaling occurs through the inhibition of C/EBPβ expression. Our data reveal a novel function of NFκB signaling in early neurogenesis and provide insight into the molecular mechanisms underlying neurodevelopmental disorders and neurodegenerative diseases.

摘要

在神经发生领域,炎症介质受到越来越多的关注,其中许多炎症介质激活了核因子 kappa B(NFκB)的信号转导。NFκB 信号转导调节轴突生长和神经可塑性,以及神经干细胞(NSC)的增殖/凋亡和终末分化。早期 NSCs 通过对称分裂产生相同的祖细胞,通过不对称分裂产生定向分化的子细胞。在这里,我们表明 NFκB 信号转导对于 NSC 的初始分化是必需的。在 TNFα 或表皮生长因子/碱性成纤维细胞生长因子去除诱导的神经分化的早期阶段,经典的 IKKβ/IκBα/p65 途径被激活。在转基因小鼠中特异性抑制 NFκB 会导致 Nestin(+) / Sox2(+) /胶质纤维酸性蛋白(+) NSCs 的积累。体外抑制 NFκB 信号转导会阻止分化和不对称分裂,并使 NSCs 保持未分化状态。NFκB 信号转导通过抑制 C/EBPβ 表达诱导初始分化和不对称性。我们的数据揭示了 NFκB 信号转导在早期神经发生中的新功能,并为神经发育障碍和神经退行性疾病的分子机制提供了深入了解。

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