Developmental Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.
Dev Cell. 2020 Nov 9;55(3):341-353.e5. doi: 10.1016/j.devcel.2020.09.030. Epub 2020 Oct 21.
FGF/ERK signaling is crucial for the patterning and proliferation of cell lineages that comprise the mouse blastocyst. However, ERK signaling dynamics have never been directly visualized in live embryos. To address whether differential signaling is associated with particular cell fates and states, we generated a targeted mouse line expressing an ERK-kinase translocation reporter (KTR) that enables live quantification of ERK activity at single-cell resolution. 3D time-lapse imaging of this biosensor in embryos revealed spatially graded ERK activity in the trophectoderm prior to overt polar versus mural differentiation. Within the inner cell mass (ICM), all cells relayed FGF/ERK signals with varying durations and magnitude. Primitive endoderm cells displayed higher overall levels of ERK activity, while pluripotent epiblast cells exhibited lower basal activity with sporadic pulses. These results constitute a direct visualization of signaling events during mammalian pre-implantation development and reveal the existence of spatial and temporal lineage-specific dynamics.
FGF/ERK 信号通路对于组成小鼠囊胚的细胞谱系的模式形成和增殖至关重要。然而,ERK 信号通路的动态变化从未在活体胚胎中直接观察到。为了确定是否存在差异性信号与特定的细胞命运和状态相关,我们构建了一个表达 ERK-激酶易位报告基因(KTR)的靶向小鼠系,该报告基因可在单细胞分辨率下实时定量 ERK 活性。对该生物传感器在胚胎中的 3D 延时成像显示,在明显的极性与壁性分化之前,滋养外胚层中存在空间梯度的 ERK 活性。在内细胞团(ICM)中,所有细胞均以不同的持续时间和幅度传递 FGF/ERK 信号。原始内胚层细胞显示出更高的 ERK 活性水平,而多能的上胚层细胞则表现出较低的基础活性,且偶有脉冲。这些结果直接观察了哺乳动物植入前发育过程中的信号事件,并揭示了空间和时间上谱系特异性动力学的存在。