Tammam Salma, Malak Peter, Correa Daphne, Rothfuss Oliver, Azzazy Hassan M E, Lamprecht Alf, Schulze-Osthoff Klaus
Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, 53121 Bonn, Germany.
Department of Chemistry, The American University in Cairo, 11835 Cairo, Egypt.
Oncotarget. 2016 Jun 21;7(25):37728-37739. doi: 10.18632/oncotarget.9276.
Protein-based reprogramming of somatic cells is a non-genetic approach for the generation of induced pluripotent stem cells (iPSCs), whereby reprogramming factors, such as OCT4, SOX2, KLF4 and c-MYC, are delivered as functional proteins. The technique is considered safer than transgenic methods, but, unfortunately, most protein-based protocols provide very low reprogramming efficiencies. In this study, we developed exemplarily a nanoparticle (NP)-based delivery system for the reprogramming factor OCT4. To this end, we expressed human OCT4 in Sf9 insect cells using a baculoviral expression system. Recombinant OCT4 showed nuclear localization in Sf9 cells indicating proper protein folding. In comparison to soluble OCT4 protein, encapsulation of OCT4 in nuclear-targeted chitosan NPs strongly stabilized its DNA-binding activity even under cell culture conditions. OCT4-loaded NPs enabled cell treatment with high micromolar concentrations of OCT4 and successfully delivered active OCT4 into human fibroblasts. Chitosan NPs therefore provide a promising tool for the generation of transgene-free iPSCs.
基于蛋白质的体细胞重编程是一种用于生成诱导多能干细胞(iPSC)的非遗传方法,通过这种方法,重编程因子,如OCT4、SOX2、KLF4和c-MYC,作为功能蛋白被递送。该技术被认为比转基因方法更安全,但不幸的是,大多数基于蛋白质的方案提供的重编程效率非常低。在本研究中,我们示例性地开发了一种用于重编程因子OCT4的基于纳米颗粒(NP)的递送系统。为此,我们使用杆状病毒表达系统在Sf9昆虫细胞中表达人OCT4。重组OCT4在Sf9细胞中显示出核定位,表明蛋白质折叠正确。与可溶性OCT4蛋白相比,即使在细胞培养条件下,将OCT4封装在核靶向壳聚糖纳米颗粒中也能强烈稳定其DNA结合活性。负载OCT4的纳米颗粒能够用高微摩尔浓度的OCT4处理细胞,并成功地将活性OCT4递送至人成纤维细胞中。因此,壳聚糖纳米颗粒为生成无转基因的iPSC提供了一种有前景的工具。