Hockemeyer Dirk, Soldner Frank, Cook Elizabeth G, Gao Qing, Mitalipova Maisam, Jaenisch Rudolf
The Whitehead Institute, 9 Cambridge Center, Cambridge, MA 02142, USA.
Department of Biology, Massachusetts Institute of Technology, 31 Ames Street, Cambridge, MA 02139 USA.
Cell Stem Cell. 2008 Sep 11;3(3):346-353. doi: 10.1016/j.stem.2008.08.014.
Current approaches to reprogram human somatic cells to pluripotent iPSCs utilize viral transduction of different combinations of transcription factors. These protocols are highly inefficient because only a small fraction of cells carry the appropriate number and stoichiometry of proviral insertions to initiate the reprogramming process. Here we have generated genetically homogeneous "secondary" somatic cells, which carry the reprogramming factors as defined doxycycline (DOX)-inducible transgenes. These cells were obtained by infecting fibroblasts with DOX-inducible lentiviruses, isolating "primary" iPSCs in the presence of the drug, and finally differentiating to "secondary" fibroblasts. When "secondary" fibroblast lines were cultured in the presence of DOX without further viral infection, up to 2% of the cells were reprogrammed to pluripotent "secondary" human iPSCs. This system will facilitate the characterization of the reprogramming process and provides a unique platform for genetic or chemical screens to enhance reprogramming or replace individual factors.
目前将人类体细胞重编程为多能诱导多能干细胞(iPSC)的方法是利用病毒转导不同组合的转录因子。这些方案效率极低,因为只有一小部分细胞携带适当数量和化学计量的前病毒插入片段来启动重编程过程。在此,我们生成了基因同质的“二级”体细胞,其携带作为强力霉素(DOX)诱导型转基因定义的重编程因子。这些细胞是通过用DOX诱导型慢病毒感染成纤维细胞、在药物存在下分离“一级”iPSC,最后分化为“二级”成纤维细胞而获得的。当“二级”成纤维细胞系在DOX存在下培养而无需进一步病毒感染时,高达2%的细胞可重编程为多能“二级”人类iPSC。该系统将有助于重编程过程的表征,并为基因或化学筛选提供独特平台,以增强重编程或替代单个因子。