Molecular and Structural Neurobiology and Gene Therapy Program, Department of Pathology and Anatomical Sciences, State University of New York, Buffalo, NY 14214, USA.
Integr Biol (Camb). 2009 Jun;1(5-6):394-403. doi: 10.1039/b902617g. Epub 2009 May 8.
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.
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。