Time-Lapse Analysis of Human Embryonic Stem Cells Reveals Multiple Bottlenecks Restricting Colony Formation and Their Relief upon Culture Adaptation

• Published in: Stem cell reports Vol. 3; no. 1; pp. 142 - 155
• Main Authors: Barbaric, Ivana, Biga, Veronica, Gokhale, Paul J., Jones, Mark, Stavish, Dylan, Glen, Adam, Coca, Daniel, Andrews, Peter W.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 08.07.2014; Elsevier
• Subjects: Cell Differentiation - physiology; Cells, Cultured; Embryonic Stem Cells - cytology; Embryonic Stem Cells - physiology; Humans; Time-Lapse Imaging
• ISSN: 2213-6711; 2213-6711
• DOI: 10.1016/j.stemcr.2014.05.006

Using time-lapse imaging, we have identified a series of bottlenecks that restrict growth of early-passage human embryonic stem cells (hESCs) and that are relieved by karyotypically abnormal variants that are selected by prolonged culture. Only a minority of karyotypically normal cells divided after plating, and these were mainly cells in the later stages of cell cycle at the time of plating. Furthermore, the daughter cells showed a continued pattern of cell death after division, so that few formed long-term proliferating colonies. These colony-forming cells showed distinct patterns of cell movement. Increasing cell density enhanced cell movement facilitating cell:cell contact, which resulted in increased proportion of dividing cells and improved survival postplating of normal hESCs. In contrast, most of the karyotypically abnormal cells reentered the cell cycle on plating and gave rise to healthy progeny, without the need for cell:cell contacts and independent of their motility patterns. [Display omitted] •The growth of karyotypically normal hESCs is limited by multiple bottlenecks•Bottlenecks include initial survival, entry into mitosis, and death following mitosis•A privileged clonogenic state in normal hESCs is characterized by distinct motility•Variant adapted cells and ROCK inhibition alleviate identified bottlenecks Andrews, Coca, and colleagues use time-lapse imaging of single human embryonic stem cells (hESCs) to identify aspects of their behavior that tend to restrict growth and so would be targets for mutations that provide selective advantage. They identify a series of bottlenecks that restricts growth of early-passage hESCs and that is relieved by karyotypically abnormal variants selected by prolonged culture.