通过纳米颗粒介导的基因转移靶向新的综合核FGFR1信号传导刺激成人大脑中的神经发生。

IF 1.4
Ewa K Stachowiak, Indrajit Roy, Yu-Wei Lee, Mariolina Capacchietti, John M Aletta, Paras N Prasad, Michal K Stachowiak
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引用次数: 39

摘要

神经发生是神经干细胞/祖细胞(NS/PC)向成熟神经元分化的过程,是治疗各种神经退行性疾病的关键,是世界人口老龄化的一个主要健康问题。我们报道了靶向新的核FGF受体1信号通路(INFS)增强NS/PCs进行神经元分化的潜在潜力,从而促进成人大脑的神经发生。利用有机修饰二氧化硅(ORMOSIL)-DNA纳米复合物有效地将重组核形式的FGFR1及其FGF-2配体转染到脑室下区,我们发现INFS刺激NS/PC退出细胞周期,分化为表达双皮质素的迁移神经母细胞和神经元,并迁移到嗅球、皮质下脑区和脑皮层。因此,纳米颗粒介导的非病毒基因转移可用于诱导NS/PCs的选择性分化,为广泛的神经系统疾病的治疗提供潜在的重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting novel integrative nuclear FGFR1 signaling by nanoparticle-mediated gene transfer stimulates neurogenesis in the adult brain.

Neurogenesis, the process of differentiation of neuronal stem/progenitor cells (NS/PC) into mature neurons, holds the key to the treatment of various neurodegenerative disorders, which are a major health issue for the world's aging population. We report that targeting the novel integrative nuclear FGF Receptor 1 signaling (INFS) pathway enhances the latent potential of NS/PCs to undergo neuronal differentiation, thus promoting neurogenesis in the adult brain. Employing organically modified silica (ORMOSIL)-DNA nanoplexes to efficiently transfect recombinant nuclear forms of FGFR1 and its FGF-2 ligand into the brain subventricular zone, we find that INFS stimulates the NS/PC to withdraw from the cell cycle, differentiate into doublecortin expressing migratory neuroblasts and neurons that migrate to the olfactory bulb, subcortical brain regions and in the brain cortex. Thus, nanoparticle-mediated non-viral gene transfer may be used to induce selective differentiation of NS/PCs, providing a potentially significant impact on the treatment of a broad range of neurological disorders.

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