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Related Experiment Video

Updated: Nov 2, 2025

Quantitative Analysis of Cell Edge Dynamics during Cell Spreading
10:54

Quantitative Analysis of Cell Edge Dynamics during Cell Spreading

Published on: May 22, 2021

5.6K

Quantitative Analysis of Cell Edge Dynamics during Cell Spreading.

Ernest Iu1, Alexander Bogatch1, Sergey V Plotnikov2

  • 1Department of Cell and Systems Biology, University of Toronto.

Journal of Visualized Experiments : Jove
|June 7, 2021
PubMed
Summary

This study details a cell spreading assay protocol and an open-source tool for analyzing cell edge dynamics. This method aids in screening molecular players that regulate lamellipodial protrusions, crucial for cell movement.

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Area of Science:

  • Cell Biology
  • Biophysics
  • Molecular Biology

Background:

  • Cell spreading involves actin polymerization in lamellipodia, essential for cell migration and endocytosis.
  • Cell spreading assays are valuable for studying lamellipodial protrusion kinetics.
  • A comprehensive protocol with data analysis tools for cell spreading assays is currently lacking.

Purpose of the Study:

  • To describe a detailed workflow for the cell spreading assay.
  • To present an open-source computational tool for quantitative analysis of cell edge dynamics.
  • To provide a method for large-scale screening of molecular regulators of lamellipodial protrusions.

Main Methods:

  • Detailed experimental procedures for the cell spreading assay.
  • Development and application of an open-source software tool for image analysis.

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Last Updated: Nov 2, 2025

Quantitative Analysis of Cell Edge Dynamics during Cell Spreading
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  • Integration with pharmacological and gene-silencing techniques.
  • Main Results:

    • A standardized protocol for performing cell spreading assays.
    • An open-source tool enabling unbiased quantification of cell edge dynamics.
    • Demonstration of the assay's utility in screening molecular players.

    Conclusions:

    • The described cell spreading assay protocol and analysis tool offer an efficient method to study lamellipodial dynamics.
    • This approach facilitates the identification of novel regulators of cell protrusion.
    • The protocol is adaptable for high-throughput screening in various cell biology research areas.