4.8 Article

Single Cell Forces after Electroporation

Journal

ACS NANO
Volume 15, Issue 2, Pages 2554-2568

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c07020

Keywords

electroporation; nanofibers; cytoskeleton; forces; mechanobiology; pulsed electric fields; actin

Funding

  1. NIH [P01CA207206]
  2. NSF [1762634]
  3. ICTAS Center for Engineered Health
  4. Directorate For Engineering
  5. Div Of Civil, Mechanical, & Manufact Inn [1762634] Funding Source: National Science Foundation

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Post-electroporation cell force undergoes three distinct stages: initial rounding and loss of contractility, followed by a biphasic stage characterized by increased contractility and subsequent force relaxation, and finally cell elongation and recovery of contractility. Increasing voltages applied perpendicular to cell orientation lead to a significant drop in cell viability, indicating that contractile force is a more sensitive metric than cell shape to electroporation.
Exogenous high-voltage pulses increase cell membrane permeability through a phenomenon known as electroporation. This process may also disrupt the cell cytoskeleton causing changes in cell contractility; however, the contractile signature of cell force after electroporation remains unknown. Here, single-cell forces post-electroporation are measured using suspended extracellular matrix-mimicking nanofibers that act as force sensors. Ten, 100 mu s pulses are delivered at three voltage magnitudes (500, 1000, and 1500 V) and two directions (parallel and perpendicular to cell orientation), exposing glioblastoma cells to electric fields between 441 V cm(-1) and 1366 V cm(-1). Cytoskeletal-driven force loss and recovery post-electroporation involves three distinct stages. Low electric field magnitudes do not cause disruption, but higher fields nearly eliminate contractility 2-10 min post-electroporation as cells round following calcium-mediated retraction (stage 1). Following rounding, a majority of analyzed cells enter an unusual and unexpected biphasic stage (stage 2) characterized by increased contractility tens of minutes post-electroporation, followed by force relaxation. The biphasic stage is concurrent with actin disruption-driven blebbing. Finally, cells elongate and regain their pre-electroporation morphology and contractility in 1-3 h (stage 3). With increasing voltages applied perpendicular to cell orientation, we observe a significant drop in cell viability. Experiments with multiple healthy and cancerous cell lines demonstrate that contractile force is a more dynamic and sensitive metric than cell shape to electroporation. A mechanobiological understanding of cell contractility post-electroporation will deepen our understanding of the mechanisms that drive recovery and may have implications for molecular medicine, genetic engineering, and cellular biophysics.

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