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通过纳米颗粒介导的基因转移靶向新型整合核 FGFR1 信号,可刺激成年大脑中的神经发生。

Targeting novel integrative nuclear FGFR1 signaling by nanoparticle-mediated gene transfer stimulates neurogenesis in the adult brain.

机构信息

Molecular and Structural Neurobiology and Gene Therapy Program, Department of Pathology and Anatomical Sciences, State University of New York, Buffalo, NY 14214, USA.

出版信息

Integr Biol (Camb). 2009 Jun;1(5-6):394-403. doi: 10.1039/b902617g. Epub 2009 May 8.

Abstract

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.

摘要

神经发生,即神经元干细胞/祖细胞(NS/PC)分化为成熟神经元的过程,是治疗各种神经退行性疾病的关键,这些疾病是世界老龄化人口的主要健康问题。我们报告称,靶向新型整合核 FGF 受体 1 信号通路(INFS)可增强 NS/PC 向神经元分化的潜在能力,从而促进成年大脑中的神经发生。我们采用有机修饰的二氧化硅(ORMOSIL)-DNA 纳米复合物将重组核形式的 FGFR1 及其 FGF-2 配体有效转染到脑室下区,发现 INFS 可刺激 NS/PC 退出细胞周期,分化为表达双皮质素的迁移性神经母细胞和神经元,这些神经元迁移到嗅球、皮质下脑区和大脑皮层。因此,纳米颗粒介导的非病毒基因转移可用于诱导 NS/PC 的选择性分化,为治疗广泛的神经退行性疾病带来潜在的重要影响。

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