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

Cell Polarization by Rho Proteins01:21

Cell Polarization by Rho Proteins

Cell polarity is the asymmetric distribution of cellular and membrane components, making one side of the cell different from the other. This polarity is essential to many processes such as embryogenesis, axon migration, glucose transport across epithelial cells, and directional cell migration. A migrating cell responds to intracellular or extracellular signals via molecular cascades that reorganize the actin cytoskeleton to establish this polarity. In these cells, the Rho family proteins Cdc42,...
Small GTPases - Ras and Rho01:24

Small GTPases - Ras and Rho

Ras and Rho are small monomeric GTPases that act downstream of receptor tyrosine kinase (RTK) and regulate various cellular processes. These GTPases switch between active and inactive states by binding to guanine nucleotides.
Three regulatory proteins control their activity:
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.
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.
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 II  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...
Cell Motility through Blebbing01:16

Cell Motility through Blebbing

Blebs are a type of membrane protrusion formed by the internal hydrostatic pressure of the cytoplasm. Blebs are observed in several cell types, including fibroblasts, immune cells, and single-celled organisms like the amoeba. The primary function of blebs is cell locomotion and apoptosis, but they are also found during necrosis and cell division. The life cycle of a bleb comprises an initiation phase followed by the expansion and retraction phases.
Blebbing Through the Matrix
In multicellular...

You might also read

Related Articles

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

Sort by
Same author

After Skin Wounding, Noncoding dsRNA Coordinates Prostaglandins and Wnts to Promote Regeneration.

The Journal of investigative dermatology·2017
Same author

Ultrasmall Semimetal Nanoparticles of Bismuth for Dual-Modal Computed Tomography/Photoacoustic Imaging and Synergistic Thermoradiotherapy.

ACS nano·2017
Same author

Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer.

Oncotarget·2017
Same author

Identification of a six-lncRNA signature associated with recurrence of ovarian cancer.

Scientific reports·2017
Same author

Ropivacaine versus levobupivacaine in peripheral nerve block: A PRISMA-compliant meta-analysis of randomized controlled trials.

Medicine·2017
Same author

Fabrication of fluorescent composite hydrogel using in situ synthesis of upconversion nanoparticles.

Nanotechnology·2017

Related Experiment Video

Updated: May 20, 2026

Ex vivo Culture of Mouse Embryonic Skin and Live-imaging of Melanoblast Migration
08:29

Ex vivo Culture of Mouse Embryonic Skin and Live-imaging of Melanoblast Migration

Published on: May 19, 2014

Melanoblasts on the move: Rac1 sets the pace.

Ang Li1, Laura M Machesky

  • 1The Beatson Institute for Cancer Research; Bearsden, Glasgow, Scotland UK.

Small Gtpases
|July 14, 2012
PubMed
Summary

Mouse melanoblasts migrate by extending dynamic pseudopodia and squeezing between cells, a process controlled by Rac1. This Rac1-dependent migration is crucial for embryonic development and may inform melanoma metastasis research.

Area of Science:

  • Developmental Biology
  • Cell Biology
  • Cancer Research

Background:

  • Cell migration is essential for embryonic development and tissue formation.
  • Cancer metastasis shares similarities with embryonic development, potentially involving reactivated developmental pathways.
  • Melanomas are highly invasive, and understanding melanoblast migration offers insights into melanoma metastasis.

Purpose of the Study:

  • To investigate the in vivo migration mechanisms of mouse melanoblasts in the epidermis.
  • To elucidate the role of Rac1 in melanoblast motility during embryonic development.

Main Methods:

  • Ex-vivo imaging of mouse melanoblast migration in the epidermis.
  • Analysis of actin-based protrusions and myosin motor involvement.
  • Assessment of Rac1's role in controlling pseudopodia formation and cell translocation.

More Related Videos

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
06:09

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells

Published on: June 7, 2019

Screening for Melanoma Modifiers using a Zebrafish Autochthonous Tumor Model
10:23

Screening for Melanoma Modifiers using a Zebrafish Autochthonous Tumor Model

Published on: November 13, 2012

Related Experiment Videos

Last Updated: May 20, 2026

Ex vivo Culture of Mouse Embryonic Skin and Live-imaging of Melanoblast Migration
08:29

Ex vivo Culture of Mouse Embryonic Skin and Live-imaging of Melanoblast Migration

Published on: May 19, 2014

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
06:09

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells

Published on: June 7, 2019

Screening for Melanoma Modifiers using a Zebrafish Autochthonous Tumor Model
10:23

Screening for Melanoma Modifiers using a Zebrafish Autochthonous Tumor Model

Published on: November 13, 2012

Main Results:

  • Mouse melanoblasts migrate individually, not collectively, using dynamic pseudopodia and squeezing between keratinocytes via myosin motors.
  • Short actin-based protrusions can form independently of Rac1.
  • Rac1 is essential for regulating the formation of long actin protrusions, enabling effective cell translocation.

Conclusions:

  • A novel Rac1-controlled in vivo migration mode has been identified in mouse melanoblasts.
  • This migration mechanism is vital for normal embryonic development.
  • Understanding this process may provide insights into melanoma invasion and metastasis.