Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, United States.
MIT Center for Precision Cancer Medicine, Massachusetts Institute of Technology, Cambridge, United States.
Elife. 2022 May 10;11:e76664. doi: 10.7554/eLife.76664.
Cell mass and composition change with cell cycle progression. Our previous work characterized buoyant mass dynamics in mitosis (Miettinen et al., 2019), but how dry mass and cell composition change in mitosis has remained unclear. To better understand mitotic cell growth and compositional changes, we develop a single-cell approach for monitoring dry mass and the density of that dry mass every ~75 s with 1.3% and 0.3% measurement precision, respectively. We find that suspension grown mammalian cells lose dry mass and increase dry mass density following mitotic entry. These changes display large, non-genetic cell-to-cell variability, and the changes are reversed at metaphase-anaphase transition, after which dry mass continues accumulating. The change in dry mass density causes buoyant and dry mass to differ specifically in early mitosis, thus reconciling existing literature on mitotic cell growth. Mechanistically, cells in early mitosis increase lysosomal exocytosis, and inhibition of lysosomal exocytosis decreases the dry mass loss and dry mass density increase in mitosis. Overall, our work provides a new approach for monitoring single-cell dry mass and dry mass density, and reveals that mitosis is coupled to extensive exocytosis-mediated secretion of cellular contents.
细胞质量和组成随细胞周期进程而变化。我们之前的工作描述了有丝分裂中悬浮质量的动力学(Miettinen 等人,2019 年),但有丝分裂中细胞的干质量和细胞组成如何变化仍不清楚。为了更好地了解有丝分裂细胞的生长和组成变化,我们开发了一种单细胞方法,以约 75 秒的时间间隔分别监测干质量及其密度,精度分别为 1.3%和 0.3%。我们发现,悬浮培养的哺乳动物细胞在进入有丝分裂后会失去干质量并增加干质量密度。这些变化显示出大的、非遗传的细胞间变异性,并且在中期-后期转变时发生逆转,之后干质量继续积累。干质量密度的变化导致有丝分裂早期的浮力和干质量出现特异性差异,从而调和了现有关于有丝分裂细胞生长的文献。从机制上讲,早期有丝分裂的细胞增加溶酶体胞吐作用,而溶酶体胞吐作用的抑制会减少有丝分裂中的干质量损失和干质量密度增加。总的来说,我们的工作提供了一种监测单细胞干质量和干质量密度的新方法,并揭示了有丝分裂与广泛的胞吐作用介导的细胞内容物分泌密切相关。