Yang Weifeng, Wei Wei, Shi Cheng, Zhu Jinliang, Ying Wenqin, Shen Yan, Ye Xin, Fang Lingling, Duo Shuguang, Che Jie, Shen Huan, Ding Sheng, Deng Hongkui
Laboratory of Stem Cell and Generative Biology, College of Life Sciences, Peking University, Beijing, China.
Stem Cells. 2009 Feb;27(2):383-9. doi: 10.1634/stemcells.2008-0974.
Most mouse embryonic stem (ES) cells are derived from a 129 or C57BL/6 background, whereas the derivation efficiency of ES cells is extremely low on certain refractory types of background for which ES cells are highly desired. Here we report an optimized, highly efficient protocol by combining pluripotin, a small molecule, and leukemia inhibitory factor (LIF) for the derivation of mouse ES cells. With this method, we successfully isolated ES cell lines from five strains of mice, with an efficiency of 57% for NOD-scid, 63% for SCID beige, 80% for CD-1, and 100% for two F1 strains from C57BL/6xCD-1. By tracking the Oct4-positive cells in the Oct4-green fluorescent protein embryos in the process of ES cell isolation, we found that pluripotin combined with LIF improved the efficiency of ES cell isolation by selectively maintaining the Oct4-positive cells in the outgrowth. To our knowledge, this is the first report of ES cells being efficiently derived from immunodeficient mice on refractory backgrounds (NOD-scid on a NOD background and SCID beige on a BALB/c background).
大多数小鼠胚胎干细胞(ES细胞)来源于129或C57BL/6背景,而在某些迫切需要ES细胞的难治性背景类型上,ES细胞的衍生效率极低。在此,我们报告一种通过结合小分子多能蛋白和白血病抑制因子(LIF)来衍生小鼠ES细胞的优化高效方案。利用这种方法,我们成功地从五个小鼠品系中分离出ES细胞系,NOD-scid的效率为57%,SCID beige的效率为63%,CD-1的效率为80%,C57BL/6×CD-1的两个F1品系的效率为100%。通过在ES细胞分离过程中追踪Oct4绿色荧光蛋白胚胎中的Oct4阳性细胞,我们发现多能蛋白与LIF相结合,通过在生长物中选择性地维持Oct4阳性细胞,提高了ES细胞的分离效率。据我们所知,这是首次报道在难治性背景(NOD背景上的NOD-scid和BALB/c背景上的SCID beige)的免疫缺陷小鼠中高效衍生ES细胞。