Quantifying the effect of electric current on cell adhesion studied by single-cell force spectroscopy

Leena Jaatinen, Eleanore Young, Jari Hyttinen, Janos Voeroes, Tomaso Zambelli, Laszlo Demko

    Research output: Contribution to journalArticleScientificpeer-review

    26 Citations (Scopus)

    Abstract

    This study presents the effect of external electric current on the cell adhesive and mechanical properties of the C2C12 mouse myoblast cell line. Changes in cell morphology, viability, cytoskeleton, and focal adhesion structure were studied by standard staining protocols, while single-cell force spectroscopy based on the fluidic force microscopy technology provided a rapid, serial quantification and detailed analysis of cell adhesion and its dynamics. The setup allowed measurements of adhesion forces up to the mu N range, and total detachment distances over 40 mu m. Force-distance curves have been fitted with a simple elastic model including a cell detachment protocol in order to estimate the Young's modulus of the cells, as well as to reveal changes in the dynamic properties as functions of the applied current dose. While the cell spreading area decreased monotonously with increasing current doses, small current doses resulted only in differences related to cell elasticity. Current doses above 11 As/m(2), however, initiated more drastic changes in cell morphology, viability, cellular structure, as well as in properties related to cell adhesion. The observed differences, eventually leading to cell death toward higher doses, might originate from both the decrease in pH and the generation of reactive oxygen species. (C) 2016 American Vacuum Society.

    Original languageEnglish
    Article number011004
    Number of pages8
    JournalBiointerphases
    Volume11
    Issue number1
    DOIs
    Publication statusPublished - Mar 2016
    Publication typeA1 Journal article-refereed

    Funding

    This work was supported by the Finnish Cultural Foundation, the Swiss National Science Foundation, and the 3DNeuroN Project in the European Unions Seventh Framework Program, Future and Emerging Technologies, Grant Agreement No. 296590. The authors thank Stephen Wheeler (ETHZ, LBB) for his valuable technical support, and acknowledge the Laboratory for Urologic Tissue Engineering and Stem Cell Therapy at the University Hospital Zurich for providing access to the fluorescent microscope used for the focal adhesion imaging, as well as Luca Hirt (ETHZ, LBB) for the idea of using the prism to take the side view images.

    Keywords

    • CALCIUM INFLUX
    • STEM-CELLS
    • FIELDS
    • MICROSCOPY
    • MECHANICS
    • MIGRATION
    • APOPTOSIS
    • GROWTH
    • PH
    • REDISTRIBUTION

    Publication forum classification

    • Publication forum level 1

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