Department for Reproductive Medicine, Ghent University Hospital, De Pintelaan 185, Ghent, Belgium.
Stem Cells Dev. 2013 Jan 15;22(2):296-306. doi: 10.1089/scd.2012.0256. Epub 2012 Aug 6.
In embryonic stem cell culture, small molecules can be used to alter key signaling pathways to promote self-renewal and inhibit differentiation. In mice, small-molecule inhibition of both the FGF/MEK/Erk and the GSK3β pathways during preimplantation development suppresses hypoblast formation, and this results in more pluripotent cells of the inner cell mass (ICM). In this study, we evaluated the effects of different small-molecule inhibitors of the FGF/MEK/Erk and GSK3β pathway on embryo preimplantation development, early lineage segregation, and subsequent embryonic stem cell derivation in the humans. We did not observe any effect on blastocyst formation, but small-molecule inhibition did affect the number of OCT3/4- and NANOG-positive cells in the human ICM. We found that combined inhibition of the FGF/MEK/Erk and GSK3β pathways by PD0325901 and CHIR99021, respectively, resulted in ICMs containing significantly more OCT3/4-positive cells. Inhibition of FGF/MEK/Erk alone as well as in combination with inhibition of GSK3β significantly increased the number of NANOG-positive cells in blastocysts possessing good-quality ICMs. Secondly, we verified the influence of this increased pluripotency after 2i culture on the efficiency of stem cell derivation. Similar human embryonic stem cell (hESC) derivation rates were observed after 2i compared to control conditions, resulting in 2 control hESC lines and 1 hESC line from an embryo cultured in 2i conditions. In conclusion, we demonstrated that FGF/MEK/Erk and GSK3β signaling increases the number of OCT3/4- and NANOG-positive cells in the human ICM, but does not improve stem cell derivation.
在胚胎干细胞培养中,可以使用小分子来改变关键信号通路,以促进自我更新并抑制分化。在小鼠中,在植入前发育过程中同时抑制 FGF/MEK/Erk 和 GSK3β 途径的小分子会抑制下胚层的形成,从而导致内细胞团 (ICM) 中的多能细胞增多。在这项研究中,我们评估了不同的 FGF/MEK/Erk 和 GSK3β 途径的小分子抑制剂对胚胎植入前发育、早期谱系分离以及随后在人类中的胚胎干细胞衍生的影响。我们没有观察到对囊胚形成有任何影响,但小分子抑制确实会影响人类 ICM 中 OCT3/4 和 NANOG 阳性细胞的数量。我们发现,分别用 PD0325901 和 CHIR99021 联合抑制 FGF/MEK/Erk 和 GSK3β 会导致 ICM 中含有更多的 OCT3/4 阳性细胞。单独抑制 FGF/MEK/Erk 以及与 GSK3β 联合抑制都会增加具有良好 ICM 的囊胚中 NANOG 阳性细胞的数量。其次,我们验证了 2i 培养后这种增加的多能性对干细胞衍生效率的影响。与对照条件相比,2i 培养后观察到类似的人类胚胎干细胞 (hESC) 衍生率,从而得到了 2 个对照 hESC 系和 1 个从 2i 条件下培养的胚胎中获得的 hESC 系。总之,我们证明 FGF/MEK/Erk 和 GSK3β 信号会增加人类 ICM 中 OCT3/4 和 NANOG 阳性细胞的数量,但不能提高干细胞的衍生效率。