Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Química Biológica, Instituto de Química Biológica (IQUIBICEN), Laboratorio de Regulación Génica en Células Madre, Buenos Aires, Argentina.
CONICET - Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI), Laboratorio de Investigación de Aplicación a Neurociencias (LIAN), Buenos Aires, Argentina.
Sci Rep. 2019 May 29;9(1):8051. doi: 10.1038/s41598-019-44537-0.
Mouse embryonic stem cells (mESCs) can be maintained as homogeneous populations in the ground state of pluripotency. Release from this state in minimal conditions allows to obtain cells that resemble those of the early post-implantation epiblast, providing an important developmental model to study cell identity transitions. However, the cell cycle dynamics of mESCs in the ground state and during its dissolution have not been extensively studied. By performing live imaging experiments of mESCs bearing cell cycle reporters, we show here that cells in the pluripotent ground state display a cell cycle structure comparable to the reported for mESCs in serum-based media. Upon release from self-renewal, the cell cycle is rapidly accelerated by a reduction in the length of the G1 phase and of the S/G2/M phases, causing an increased proliferation rate. Analysis of cell lineages indicates that cell cycle variables of sister cells are highly correlated, suggesting the existence of inherited cell cycle regulators from the parental cell. Together with a major morphological reconfiguration upon differentiation, our findings support a correlation between this in vitro model and early embryonic events.
小鼠胚胎干细胞(mESCs)可在多能性的基础状态下维持为同质群体。在最小条件下从这种状态释放出来,可以获得类似于早期着床后胚外层的细胞,为研究细胞身份转变提供了一个重要的发育模型。然而,mESCs 在基础状态下和在其溶解过程中的细胞周期动力学尚未得到广泛研究。通过对带有细胞周期报告基因的 mESCs 进行活细胞成像实验,我们在这里表明,多能性基础状态下的细胞显示出与在基于血清的培养基中报道的 mESCs 相当的细胞周期结构。从自我更新中释放出来后,细胞周期通过减少 G1 期和 S/G2/M 期的长度而迅速加速,导致增殖率增加。细胞谱系分析表明,姐妹细胞的细胞周期变量高度相关,表明存在来自亲本细胞的遗传细胞周期调节剂。与分化时的主要形态重构一起,我们的发现支持了该体外模型与早期胚胎事件之间的相关性。