Cortical waves mediate the cellular response to electric fields

Author:

Yang Qixin,Miao Yuchuan,Campanello Leonard J.,Hourwitz Matt J.,Abubaker-Sharif Bedri,Bull Abby L.,Devreotes Peter N.,Fourkas John T.,Losert Wolfgang

Abstract

AbstractElectrotaxis, the directional migration of cells in a constant electric field, is important in regeneration, development, and wound healing. Electrotaxis has a slower response and a smaller dynamic range than guidance by other cues, suggesting that the mechanism of electrotaxis share both similarities and differences with chemical-gradient-sensing pathways. We examined a mechanism centered on the excitable system consisting of cortical waves of biochemical signals coupled to cytoskeletal reorganization, which has been implicated in random cell motility. We use electro-fused giant Dictyostelium discoideum cells to decouple waves from cell motion and employ nanotopographic surfaces to limit wave dimensions and lifetimes. We demonstrate that wave propagation in these cells is guided by electric fields. The wave area and lifetime gradually increase in the first 10 minutes after an electric field is turned on, leading to more abundant and wider protrusions in the cell region nearest the cathode. The wave directions display “U-turn” behavior upon field reversal, and this switch occurs more quickly on nanotopography. Our results suggest that electric fields guide cells by controlling waves of signal transduction and cytoskeletal activity, which underlie cellular protrusions. Whereas surface receptor occupancy triggers both rapid activation and slower polarization of signaling pathways, electric fields appear to act primarily on polarization, explaining why cells respond to electric fields more slowly than to other guidance cues.

Publisher

Cold Spring Harbor Laboratory

Reference46 articles.

1. Electrophoresis of Cellular Membrane Components Creates the Directional Cue Guiding Keratocyte Galvanotaxis

2. Traveling and standing waves mediate pattern formation in cellular protrusions;Science Advances,2020

3. Controlling excitable wave behaviors through the tuning of three parameters;Biological Cybernetics,2018

4. A Coupled Excitable Network Model Dictates Cortical Wave Patterns and Controls Cellular Protrusion Morphology;Biophysical Journal,2019

5. The Three-Dimensional Dynamics of Actin Waves, a Model of Cytoskeletal Self-Organization

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