Failed mitotic exit in Human Umbilical Vein Endothelial Cells

Human Umbilical Vein Endothelial Cells (HUVECs) were first cultured in 1973[1]. Since then, their isolation protocols have improved and they have become a model system for the study of a variety of vascular pathologies, such as inflammatory disease, atherosclerosis and cancer.

Endothelial cells are found in the inner layer of both blood and lymphatic vessels and they play a role in substance transport and in a variety of other physiological processes[2].

Two samples of cryopreserved HUVEC culture from a single donor, and kindly provided by Promocell GmbH[3] were observed under Nanolive’s 3D Cell Explorer.


One of the samples led to the observation of a mitotic process (left on the footage). As described in our previous post featuring Mesenchymal Stem Cells, cell division is a strongly regulated process that ensures growth, wound healing and replacement of damaged cells in eukaryotic cells.

During the live cell imaging of the sample we could observe chromatin condensation, chromosome alineation in the metaphase plate, chromatids migration and the formation of the contractile ring and further separation in two fully functional daughter cells.

Mitosis Abortion

Mitotic exit is controlled by proteolysis[4], [5] and the activity of cyclin dependent kinases (CDKs) that play a key role in anaphase spindle formation and the onset of cytokinesis[4]–[7].

This mitosis regulation machinery can sometimes detect errors that may influence mitosis progression and exit, forcing a revert into interphase[4].

On the right side of the footage, the observed cell seems to enter mitosis, but the chromatids do not complete segregation and the cell goes back to interphase without dividing.


[1]         E. A. Jaffe, R. L. Nachman, C. G. Becker, and C. R. Minick, “Culture of Human Endothelial Cells Derived from Umbilical Veins. IDENTIFICATION BY MORPHOLOGIC AND IMMUNOLOGIC CRITERIA,” J. Clin. Invest., vol. 52, no. 11, pp. 2745–2756, Nov. 1973.

[2]         C. Michiels, “Endothelial cell functions,” J. Cell. Physiol., vol. 196, no. 3, pp. 430–443, Sep. 2003.

[3]         “HUVEC: Human Umbilical Vein Endothelial Cells | PromoCell.” [Online]. Available: [Accessed: 09-Aug-2019].

[4]         F. Wolf, R. Sigl, and S. Geley, “‘… The end of the beginning’: cdk1 thresholds and exit from mitosis.,” Cell Cycle, vol. 6, no. 12, pp. 1408–11, Jun. 2007.

[5]         T. A. Potapova et al., “The reversibility of mitotic exit in vertebrate cells,” Nature, vol. 440, no. 7086, pp. 954–958, Apr. 2006.

[6]         L. Trinkle-Mulcahy and A. I. Lamond, “Mitotic phosphatases: no longer silent partners,” Curr. Opin. Cell Biol., vol. 18, no. 6, pp. 623–631, Dec. 2006.

[7]         D. H. Parry, G. R. X. Hickson, and P. H. O’Farrell, “Cyclin B destruction triggers changes in kinetochore behavior essential for successful anaphase.,” Curr. Biol., vol. 13, no. 8, pp. 647–53, Apr. 2003.

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11 Scientific publications featuring Nanolive live cell imaging

11 Scientific publications featuring Nanolive live cell imaging

April and May have been busy months for our clients with 11 new scientific publications since our last update featuring Nanolive live cell imaging. Most articles were either immuno-oncology & oncology or microbiology & biofilm-related, but there was a sprinkle...

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