Stem Cells and Neurogenesis Unit, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
PLoS One. 2010 Dec 30;5(12):e16092. doi: 10.1371/journal.pone.0016092.
Recent data demonstrates that stem cells can exist in two morphologically, molecularly and functionally distinct pluripotent states; a naïve LIF-dependent pluripotent state which is represented by murine embryonic stem cells (mESCs) and an FGF-dependent primed pluripotent state represented by murine and rat epiblast stem cells (EpiSCs). We find that derivation of induced pluripotent stem cells (iPSCs) under EpiSC culture conditions yields FGF-dependent iPSCs from hereon called FGF-iPSCs) which, unexpectedly, display naïve ES-like/ICM properties. FGF-iPSCs display X-chromosome activation, multi-lineage differentiation, teratoma competence and chimera contribution in vivo. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions. Characterization of the key molecular signalling pathways revealed FGF-iPSCs to depend on the Activin/Nodal and FGF pathways, while signalling through the JAK-STAT pathway is not required for FGF-iPS cell maintenance. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions.
最近的数据表明,干细胞可以存在于两种形态、分子和功能上不同的多能状态中;一种是原始的 LIF 依赖性多能状态,由小鼠胚胎干细胞(mESCs)代表,另一种是由小鼠和大鼠上胚层干细胞(EpiSCs)代表的 FGF 依赖性初始多能状态。我们发现,在 EpiSC 培养条件下诱导多能干细胞(iPSCs)的衍生产生了 FGF 依赖性 iPSCs(以下简称 FGF-iPSCs),它们出人意料地表现出原始 ES 样/ICM 特性。FGF-iPSCs 表现出 X 染色体激活、多能性分化、畸胎瘤能力和体内嵌合体贡献。我们的研究结果表明,在 129 和 Bl6 小鼠品系中,iPSCs 可以在不依赖于培养生长因子条件的情况下,主要采用原始的多能状态。对关键分子信号通路的特征分析表明,FGF-iPSCs 依赖于 Activin/Nodal 和 FGF 通路,而 JAK-STAT 通路的信号传导对于 FGF-iPS 细胞的维持不是必需的。我们的研究结果表明,在 129 和 Bl6 小鼠品系中,iPSCs 可以在不依赖于培养生长因子条件的情况下,主要采用原始的多能状态。