AMOLF, Science Park 104, 1098 XG Amsterdam, the Netherlands.
AMOLF, Science Park 104, 1098 XG Amsterdam, the Netherlands.
Cell Syst. 2017 Feb 22;4(2):219-230.e6. doi: 10.1016/j.cels.2017.01.009. Epub 2017 Feb 15.
It is a fundamental open question as to how embryos develop into complex adult organisms with astounding reproducibility, particularly because cells are inherently variable on the molecular level. During C. elegans vulva induction, the anchor cell induces cell fate in the vulva precursor cells in a distance-dependent manner. Surprisingly, we found that initial anchor cell position was highly variable and caused variability in cell fate induction. However, we observed that vulva induction was "canalized," i.e., the variability in anchor cell position and cell fate was progressively reduced, resulting in an invariant spatial pattern of cell fates at the end of induction. To understand the mechanism of canalization, we quantified induction dynamics as a function of anchor cell position during the canalization process. Our experiments, combined with mathematical modeling, showed that canalization required a specific combination of long-range induction, lateral inhibition, and cell migration that is also found in other developmental systems.
胚胎如何发育成具有惊人重现性的复杂成年生物体是一个基本的开放性问题,特别是因为细胞在分子水平上固有地具有变异性。在秀丽隐杆线虫的外阴诱导过程中,锚定细胞以距离依赖的方式诱导外阴前体细胞的细胞命运。令人惊讶的是,我们发现初始锚定细胞位置高度可变,导致细胞命运诱导的可变性。然而,我们观察到外阴诱导是“管道化”的,即锚定细胞位置和细胞命运的可变性逐渐降低,导致诱导结束时细胞命运的空间模式不变。为了理解管道化的机制,我们在管道化过程中定量了锚定细胞位置对诱导动力学的影响。我们的实验结合数学建模表明,管道化需要长程诱导、侧向抑制和细胞迁移的特定组合,这种组合也存在于其他发育系统中。