ArticlePloS one2014
Live cell interferometry quantifies dynamics of biomass partitioning during cytokinesis.
Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 23 citations in OpenAlex.
- Label-free interferometry platform for drug response profiling of bioprinted tumor organoids at single-organoid resolution.Nature protocols · 2026Review
- Determination of Drug Sensitivity in Patient Derived Models of Breast Cancer by Multiparametric QPI.bioRxiv : the preprint server for biology · 2025Article
- Tracking of lineage massLab on a chip · 2024Article
- Drug screening at single-organoid resolution via bioprinting and interferometry.Nature communications · 2023Article
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- Review
- Rapid, label-free classification of tumor-reactive T cell killing with quantitative phase microscopy and machine learning.Scientific reports · 2021Article
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- Cell viscoelasticity is linked to fluctuations in cell biomass distributions.Scientific reports · 2020Article
- Identifying fates of cancer cells exposed to mitotic inhibitors by quantitative phase imaging.The Analyst · 2019Article
- Ampk regulates IgD expression but not energy stress with B cell activation.Scientific reports · 2019Article
- Deep Learning in Label-free Cell Classification.Scientific reports · 2016Article
- Hybrid random walk-linear discriminant analysis method for unwrapping quantitative phase microscopy images of biological samples.Journal of biomedical optics · 2015Article
Corrections and comments
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Authors and funding
3 authors at 3 institutions in 1 country.
Funding
Abstract
The equal partitioning of cell mass between daughters is the usual and expected outcome of cytokinesis for self-renewing cells. However, most studies of partitioning during cell division have focused on daughter cell shape symmetry or segregation of chromosomes. Here, we use live cell interferometry (LCI) to quantify the partitioning of daughter cell mass during and following cytokinesis. We use adherent and non-adherent mouse fibroblast and mouse and human lymphocyte cell lines as models and show that, on average, mass asymmetries present at the time of cleavage furrow formation persist through cytokinesis. The addition of multiple cytoskeleton-disrupting agents leads to increased asymmetry in mass partitioning which suggests the absence of active mass partitioning mechanisms after cleavage furrow positioning.
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Registered trials
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