Elasticity and tumorigenic characteristics of cells in a monolayer after nanosecond pulsed electric field exposure

Investor logo

Warning

This publication doesn't include Faculty of Arts. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

STEUER A. WENDE K. BABICA Pavel KOLB J. F.

Year of publication 2017
Type Article in Periodical
Magazine / Source European Biophysics Journal With Biophysics Letters
MU Faculty or unit

Faculty of Science

Citation
Web https://link.springer.com/article/10.1007%2Fs00249-017-1205-y
Doi http://dx.doi.org/10.1007/s00249-017-1205-y
Keywords nsPEF; Elasticity; Elastic modulus; AFM; Actin cytoskeleton; Anchorage-independent growth
Description Nanosecond pulsed electric fields (nsPEFs) applied to cells can induce different biological effects depending on pulse duration and field strength. One known process is the induction of apoptosis whereby nsPEFs are currently investigated as a novel cancer therapy. Another and probably related change is the breakdown of the cytoskeleton. We investigated the elasticity of rat liver epithelial cells WB-F344 in a monolayer using atomic force microscopy (AFM) with respect to the potential of cells to undergo malignant transformation or to develop a potential to metastasize. We found that the elastic modulus of the cells decreased significantly within the first 8 min after treatment with 20 pulses of 100 ns and with a field strength of 20 kV/cm but was still higher than the elasticity of their tumorigenic counterpart WB-ras. AFM measurements and immunofluorescent staining showed that the cellular actin cytoskeleton became reorganized within 5 min. However, both a colony formation assay and a cell migration assay revealed no significant changes after nsPEF treatment, implying that cells seem not to adopt malignant characteristics associated with metastasis formation despite the induced transient changes to elasticity and cytoskeleton that can be observed for up to 1 h.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.