Department of Genetics and Bioengineering, Faculty of Engineering, Yeditepe University, Istanbul, Turkey.
Methods Mol Biol. 2022;2520:101-115. doi: 10.1007/7651_2021_402.
Mouse embryonic stem cells (mESCs) were first derived and cultured nearly 30 years ago and have been beneficial tools to create transgenic mice and to study early mammalian development so far. Fibroblast feeder cell layers are often used at some stage in the culture protocol of mESCs. The feeder layer-often mouse embryonic fibroblasts (MEFs)-contribute to the mESC culture as a substrate to increase culture efficiency, maintain pluripotency, and facilitate survival and growth of the stem cells. Various feeder-dependent and feeder-independent culture and differentiation protocols have been established for mESCs. Here we describe the isolation, culture, and preparation feeder cell layers and establishment of feeder-dependent/independent protocol for mESC culture. In addition, basic mESC protocols for culture, storage, and differentiation were described.
小鼠胚胎干细胞(mESCs)于近 30 年前首次被分离和培养,迄今为止一直是用于创建转基因小鼠和研究早期哺乳动物发育的有益工具。在 mESC 的培养方案的某个阶段,通常会使用成纤维细胞饲养层。饲养层-通常是小鼠胚胎成纤维细胞(MEFs)-作为基质有助于 mESC 的培养,提高培养效率,维持多能性,并促进干细胞的存活和生长。已经建立了各种依赖饲养层和不依赖饲养层的 mESC 培养和分化方案。在这里,我们描述了饲养层细胞的分离、培养和制备,以及建立 mESC 培养的依赖/不依赖饲养层的方案。此外,还描述了基本的 mESC 培养、储存和分化方案。