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Mouse embryonic stem cells resist c-Jun induced differentiation when in suspension

机译:悬浮状态下小鼠胚胎干细胞抵抗c-Jun诱导的分化

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摘要

The oncogene c-Jun plays a key role in development and cancer. Yet, its role in cell fate decision remains poorly understood at the molecular level. Here we report that c-Jun confers different fate decisions upon mouse embryonic stem cells (mESCs) in adhesion vs suspension culture. We developed a Tet-on system for temporal induction of c-Jun expression by Doxycycline treatment in mESCs. We show that mESCs carrying the inducible c-Jun TetOn remain pluripotent and grow slowly in suspension when c-Jun expression is induced, whilst when the cells adhere they undergo differentiation and show normal proliferative potential upon c-Jun induction. Our data indicates that c-Jun pushes mESCs in suspension into cell cycle arrest at G1/S, by activating the cell cycle inhibitors Cdkn1a/b and Cdkn2/a/b/c. Despite this cell cycle arrest, they can still re-enter the cell cycle upon transfer to an adhesive surface, and grow into typical mESC colonies, albeit at a lower efficiency. These results demonstrate that mESCs respond to induced c-Jun overexpression differently in suspension or adherent cultures. Our results suggest that cells in suspension may be more resistant to differentiation than when they adhere.
机译:癌基因c-Jun在发展和癌症中起关键作用。然而,它在细胞命运决定中的作用在分子水平上仍然知之甚少。在这里我们报告c-Jun在粘附与悬浮培养中赋予小鼠胚胎干细胞(mESCs)不同的命运决定。我们开发了一种Tet-on系统,用于通过强力霉素处理在mESC中暂时诱导c-Jun表达。我们显示,携带可诱导的c-Jun TetOn的mESCs在诱导c-Jun表达时保持多能性并在悬浮液中缓慢生长,而当细胞粘附时,它们会分化并在c-Jun诱导后显示正常的增殖潜能。我们的数据表明,c-Jun通过激活细胞周期抑制剂Cdkn1a / b和Cdkn2 / a / b / c将悬浮的mESC推入G1 / S的细胞周期停滞期。尽管有这种细胞周期停滞,但它们仍然可以在转移到粘附表面后重新进入细胞周期,并生长成典型的mESC集落,尽管效率较低。这些结果表明,mESC在悬浮培养或贴壁培养中对诱导的c-Jun过表达的反应不同。我们的结果表明,悬浮中的细胞可能比粘附时更具抗分化能力。

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