Cambuli Francesco, Murray Alexander, Dean Wendy, Dudzinska Dominika, Krueger Felix, Andrews Simon, Senner Claire E, Cook Simon J, Hemberger Myriam
1] Epigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK [2] Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Epigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.
Nat Commun. 2014 Nov 26;5:5538. doi: 10.1038/ncomms6538.
Embryonic (ES) and trophoblast (TS) stem cells reflect the first, irrevocable cell fate decision in development that is reinforced by distinct epigenetic lineage barriers. Nonetheless, ES cells can seemingly acquire TS-like characteristics upon manipulation of lineage-determining transcription factors or activation of the extracellular signal-regulated kinase 1/2 (Erk1/2) pathway. Here we have interrogated the progression of reprogramming in ES cell models with regulatable Oct4 and Cdx2 transgenes or conditional Erk1/2 activation. Although trans-differentiation into TS-like cells is initiated, lineage conversion remains incomplete in all models, underpinned by the failure to demethylate a small group of TS cell genes. Forced expression of these non-reprogrammed genes improves trans-differentiation efficiency, but still fails to confer a stable TS cell phenotype. Thus, even ES cells in ground-state pluripotency cannot fully overcome the boundaries that separate the first cell lineages but retain an epigenetic memory of their ES cell origin.
胚胎干细胞(ES)和滋养层干细胞(TS)反映了发育过程中第一个不可逆转的细胞命运决定,这种决定由独特的表观遗传谱系屏障强化。尽管如此,在操纵谱系决定转录因子或激活细胞外信号调节激酶1/2(Erk1/2)通路后,ES细胞似乎能够获得类似TS细胞的特征。在这里,我们利用可调控的Oct4和Cdx2转基因或条件性Erk1/2激活,研究了ES细胞模型中的重编程进程。尽管开始了向类似TS细胞的转分化,但在所有模型中谱系转换仍然不完全,这是由于一小部分TS细胞基因未能去甲基化所致。强制表达这些未重编程的基因可提高转分化效率,但仍无法赋予稳定的TS细胞表型。因此,即使是处于基础多能性状态的ES细胞也无法完全跨越分隔第一个细胞谱系的边界,而是保留了其ES细胞起源的表观遗传记忆。