Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK; Division of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, The University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Division of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, The University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Dev Cell. 2018 Nov 19;47(4):494-508.e4. doi: 10.1016/j.devcel.2018.09.023. Epub 2018 Oct 25.
Cell-cell heterogeneity can facilitate lineage choice during embryonic development because it primes cells to respond to differentiation cues. However, remarkably little is known about the origin of heterogeneity or whether intrinsic and extrinsic variation can be controlled to generate reproducible cell type proportioning seen in vivo. Here, we use experimentation and modeling in D. discoideum to demonstrate that population-level cell cycle heterogeneity can be optimized to generate robust cell fate proportioning. First, cell cycle position is quantitatively linked to responsiveness to differentiation-inducing signals. Second, intrinsic variation in cell cycle length ensures cells are randomly distributed throughout the cell cycle at the onset of multicellular development. Finally, extrinsic perturbation of optimal cell cycle heterogeneity is buffered by compensatory changes in global signal responsiveness. These studies thus illustrate key regulatory principles underlying cell-cell heterogeneity optimization and the generation of robust and reproducible fate choice in development.
细胞间的异质性可以促进胚胎发育过程中的谱系选择,因为它使细胞能够对分化信号做出反应。然而,关于异质性的起源,或者是否可以控制内在和外在的变化以产生体内所见的可重复的细胞类型比例,人们知之甚少。在这里,我们使用 D. discoideum 的实验和建模来证明群体水平的细胞周期异质性可以被优化,以产生稳健的细胞命运比例。首先,细胞周期位置与对分化诱导信号的反应性定量相关。其次,细胞周期长度的内在变化确保了在多细胞发育开始时,细胞随机分布在整个细胞周期中。最后,通过对最佳细胞周期异质性的外部干扰进行缓冲,从而实现了全局信号反应性的补偿变化。因此,这些研究说明了细胞间异质性优化和发育中稳健和可重复的命运选择的关键调节原则。