Functional interplay between the cell cycle and cell phenotypes

被引:23
作者
Chen, Wei-Chiang [1 ,2 ]
Wu, Pei-Hsun [1 ,2 ]
Phillip, Jude M. [1 ,2 ]
Khatau, Shyam B. [1 ,2 ]
Choi, Jae Min [2 ]
Dallas, Matthew R. [1 ,2 ]
Konstantopoulos, Konstantinos [1 ,2 ]
Sun, Sean X. [1 ,3 ]
Lee, Jerry S. H. [2 ,4 ]
Hodzic, Didier [5 ]
Wirtz, Denis [1 ,2 ]
机构
[1] Johns Hopkins Univ, Johns Hopkins Phys Sci Oncol Ctr, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Mech Engn, Baltimore, MD 21218 USA
[4] NCI, Ctr Strateg Sci Initiat, Off Director, NIH, Bethesda, MD 20892 USA
[5] Washington Univ, Sch Med, Dept Ophthalmol, St Louis, MO 63110 USA
基金
美国国家科学基金会;
关键词
DISTINCT ROLES; FIBROBLASTS; CONNECTIONS; PROGRESSION; CANCER; ACTIN; SYNCHRONIZATION; RESOLUTION; INHIBITOR; NUCLEUS;
D O I
10.1039/c2ib20246h
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cell cycle distribution of adherent cells is typically assessed using flow cytometry, which precludes the measurements of many cell properties and their cycle phase in the same environment. Here we develop and validate a microscopy system to quantitatively analyze the cell-cycle phase of thousands of adherent cells and their associated cell properties simultaneously. This assay demonstrates that population-averaged cell phenotypes can be written as a linear combination of cell-cycle fractions and phase-dependent phenotypes. By perturbing the cell cycle through inhibition of cell-cycle regulators or changing nuclear morphology by depletion of structural proteins, our results reveal that cell cycle regulators and structural proteins can significantly interfere with each other's prima facie functions. This study introduces a high-throughput method to simultaneously measure the cell cycle and phenotypes at single-cell resolution, which reveals a complex functional interplay between the cell cycle and cell phenotypes.
引用
收藏
页码:523 / 534
页数:12
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