Department of Genetics & Center for Stem Cell and Regenerative Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
Cell Stem Cell. 2011 Mar 4;8(3):318-25. doi: 10.1016/j.stem.2011.01.016.
Pluripotent stem cells provide a platform to interrogate control elements that function to generate all cell types of the body. Despite their utility for modeling development and disease, the relationship of mouse and human pluripotent stem cell states to one another remains largely undefined. We have shown that mouse embryonic stem (ES) cells and epiblast stem cells (EpiSCs) are distinct, pluripotent states isolated from pre- and post-implantation embryos respectively. Human ES cells are different than mouse ES cells and share defining features with EpiSCs, yet are derived from pre-implantation human embryos. Here we show that EpiSCs can be routinely derived from pre-implantation mouse embryos. The preimplantation-derived EpiSCs exhibit molecular features and functional properties consistent with bona fide EpiSCs. These results provide a simple method for isolating EpiSCs and offer direct insight into the intrinsic and extrinsic mechanisms that regulate the acquisition of distinct pluripotent states.
多能干细胞为研究控制元件提供了一个平台,这些控制元件的功能是产生身体的所有细胞类型。尽管它们在模拟发育和疾病方面具有实用性,但小鼠和人类多能干细胞状态之间的关系在很大程度上仍未得到明确界定。我们已经表明,小鼠胚胎干细胞(ES 细胞)和胚胎外干细胞(EpiSCs)是分别从着床前和着床后胚胎中分离出来的不同的多能状态。人类 ES 细胞不同于小鼠 ES 细胞,与 EpiSCs 具有共同的特征,但来源于着床前的人类胚胎。在这里,我们表明可以常规地从着床前的小鼠胚胎中分离出 EpiSCs。这种由着床前胚胎衍生的 EpiSCs 表现出与真正的 EpiSCs 一致的分子特征和功能特性。这些结果提供了一种简单的方法来分离 EpiSCs,并为研究内在和外在调控机制以获得不同的多能状态提供了直接的见解。