Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Chemotaxis and Direction of Cell Migration01:21

Chemotaxis and Direction of Cell Migration

Cells can detect chemical cues in their environment and reorganize the cytoskeleton to migrate toward them or away from them. This directional migration, called chemotaxis, is essential during embryogenesis and development, immune response, tissue repair and regeneration, and reproduction. These chemical cues can either attract or repel the cell's movement. For example, axon development is determined by a combination of chemoattractants and chemorepellents that direct the growing axon towards...
Cell Migration01:09

Cell Migration

Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms throughout their life. When cells are not able to migrate properly to their ordained locations, various disorders may occur. For example, disruption in cell migration causes chronic inflammatory diseases such as arthritis.
Cell Migration01:19

Cell Migration

Cell migration is a process by which the cells move from one location to another, playing an essential role in embryological development, repair and regeneration, immune response, and metastasis. Cells migrate in response to chemical or mechanical signals generated by specific organs or tissues. The overall mechanism includes three steps - polarization, protrusion, and release. Polarization involves the formation of a distinct cell front and rear, which determines the direction of movement.
Actin Polymerization and Cell Motility01:13

Actin Polymerization and Cell Motility

Actin is a family of globular proteins that are highly abundant in eukaryotic cells. It makes up approximately 1-5% of total cell protein concentration. Actin monomers polymerize to form a complex network of polarized filaments, the actin cytoskeleton, that plays a crucial role in many cellular processes, including cell motility, division, endocytosis, and metastasis of cancer cells.
Actin cytoskeleton dynamics can produce pushing, pulling, and resistance forces that help the cell to migrate.
Chemotaxis in E. coli01:27

Chemotaxis in E. coli

Chemotaxis in Escherichia coli is a sensory-driven motility mechanism that enables bacteria to navigate chemical gradients, moving toward beneficial environments while avoiding harmful conditions. This process relies on a signal transduction system integrating external chemical cues with flagellar motor control.Chemoreceptors and Signal DetectionE. coli detects chemical gradients through methyl-accepting chemotaxis proteins (MCPs), which are membrane-bound chemoreceptors that sense attractants...
Role of Myosin in Cell Migration01:18

Role of Myosin in Cell Migration

Myosins are multimeric motor proteins involved in various cellular processes such as migration, adhesion, and proliferation. Myosin II is the most common type in animal cells, which binds and cross-links actin filaments.
Myosin IIĀ  is a hexamer comprising two heavy chains with globular heads and coiled-coil tails, two regulatory light chains, and two essential light chains. The ATPase sites on the myosin heads hydrolyze ATP, and the released phosphate generates the force for contraction. It is...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Ecological dynamics of pro-tumor and anti-tumor teams in the tumor microenvironment.

Physical biologyĀ·2026
Same author

Rewiring miR-22/SNAI1 via CRISPR-based edge editing destabilizes the epithelial phenotype.

NPJ systems biology and applicationsĀ·2026
Same author

Phase-field approach to cellular blebbing.

Physical review. EĀ·2026
Same author

A biophysical framework for accurately identifying antigen single-amino acid escape variants and corresponding variant-specific compensatory TCR sequences.

bioRxiv : the preprint server for biologyĀ·2026
Same author

The interaction between dynamic ligand signaling and epigenetics in Notch-induced cancer metastasis.

Physical biologyĀ·2025
Same author

A multilevel formalism to model the hybrid E/M phenotypes in epithelial-mesenchymal plasticity.

Biophysical journalĀ·2025

Related Experiment Video

Updated: May 31, 2026

Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells
08:24

Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells

Published on: September 14, 2016

Activated membrane patches guide chemotactic cell motility.

Inbal Hecht1, Monica L Skoge, Pascale G Charest

  • 1Center for Theoretical Biological Physics, University of California San Diego, La Jolla, California, United States of America. inbal.hecht@gmail.com

Plos Computational Biology
|July 9, 2011
PubMed
Summary

Cellular crawling relies on signaling patches that guide membrane protrusions. This study models how RasGTP localization drives amoeboid cell motion and pseudopod dynamics.

More Related Videos

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation
10:40

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation

Published on: November 9, 2017

Imaging G-protein Coupled Receptor (GPCR)-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum
09:40

Imaging G-protein Coupled Receptor (GPCR)-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum

Published on: September 20, 2011

Related Experiment Videos

Last Updated: May 31, 2026

Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells
08:24

Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells

Published on: September 14, 2016

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation
10:40

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation

Published on: November 9, 2017

Imaging G-protein Coupled Receptor (GPCR)-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum
09:40

Imaging G-protein Coupled Receptor (GPCR)-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum

Published on: September 20, 2011

Area of Science:

  • Cell Biology
  • Biophysics
  • Computational Biology

Background:

  • Eukaryotic cells exhibit directed motility (crawling) guided by environmental cues.
  • Cellular signaling systems interpret cues, coupling to cell mechanics and forming activated membrane patches.
  • These patches, areas of concentrated signaling components, are linked to membrane protrusions.

Purpose of the Study:

  • To investigate the relationship between activated signaling patches and cell motion.
  • To examine the spatial localization of RasGTP in chemotaxing Dictyostelium discoideum cells.
  • To develop and validate a model for amoeboid cell motion.

Main Methods:

  • Quantitative analysis of RasGTP spatial localization in restricted-height Dictyostelium discoideum cells.
  • Formulation of a two-module computational model for cell motility.
  • Incorporation of a reaction-diffusion model for signaling patch dynamics and a mechanics module for protrusion formation.

Main Results:

  • High spatial correlation observed between activated Ras patches and membrane protrusions.
  • The model successfully generated realistic amoeboid-like motion.
  • Numerical results align with experimental observations of pseudopod dynamics, including splitting.

Conclusions:

  • Activated signaling patches, specifically RasGTP, are key drivers of amoeboid cell motion.
  • The developed model accurately simulates cell crawling behavior and pseudopod dynamics.
  • Signaling patch dynamics can directly explain phenomena like pseudopod splitting.