Single-cell monitoring of dry mass and dry mass density reveals exocytosis of cellular dry contents in mitosis

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.

Automated summary

This study reveals that mammalian cells lose dry mass and increase dry mass density upon entering mitosis, with large non-genetic variability. These changes are reversed at the metaphase-anaphase transition, and dry mass continues to accumulate. Early mitotic cells increase lysosomal exocytosis, and inhibition of this process reduces dry mass loss and dry mass density increase. Overall, this work provides a new method for monitoring single-cell dry mass and density, and uncovers the connection between mitosis and extensive exocytosis-mediated secretion of cellular contents.