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Cell Migration

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Cover of 'Cell Migration'

Table of Contents

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    Book Overview
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    Chapter 1 Random Migration Assays of Mammalian Cells and Quantitative Analyses of Single Cell Trajectories
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    Chapter 2 Directional Collective Migration in Wound Healing Assays
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    Chapter 3 An In Vitro System to Study the Mesenchymal-to-Amoeboid Transition
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    Chapter 4 An In Vitro System to Study the Epithelial–Mesenchymal Transition In Vitro
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    Chapter 5 Detection of Migrasomes
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    Chapter 6 3D Endothelial Cell Migration
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    Chapter 7 Transmigration of Leukocytes Across Epithelial Monolayers
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    Chapter 8 Evaluation of Tumor Cell Invasiveness In Vivo: The Chick Chorioallantoic Membrane Assay
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    Chapter 9 Analysis of Invasion Dynamics of Matrix-Embedded Cells in a Multisample Format
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    Chapter 10 Using Systems Microscopy to Understand the Emergence of Cell Migration from Cell Organization
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    Chapter 11 Neuronal Precursor Migration in Ex Vivo Brain Slice Culture
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    Chapter 12 In Vitro Models to Analyze the Migration of MGE-Derived Interneurons
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    Chapter 13 Cell Migration in Tissues: Explant Culture and Live Imaging
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    Chapter 14 Intravital Imaging of Tumor Cell Motility in the Tumor Microenvironment Context
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    Chapter 15 Using the Zebrafish Embryo to Dissect the Early Steps of the Metastasis Cascade
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    Chapter 16 Analysis of In Vivo Cell Migration in Mosaic Zebrafish Embryos
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    Chapter 17 Analysis of Cell Shape and Cell Migration of Drosophila Macrophages In Vivo
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    Chapter 18 Migration of Q Cells in Caenorhabditis elegans
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    Chapter 19 Imaging the Molecular Machines That Power Cell Migration
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    Chapter 20 A Biologist-Friendly Method to Analyze Cross-Correlation Between Protrusion Dynamics and Membrane Recruitment of Actin Regulators
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    Chapter 21 Using Single-Protein Tracking to Study Cell Migration
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    Chapter 22 Optogenetic Control of Cell Migration
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    Chapter 23 Electrotaxis: Cell Directional Movement in Electric Fields
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    Chapter 24 Analysis of Random Migration of Dictyostelium Amoeba in Confined and Unconfined Environments
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    Chapter 25 Neutrophil Chemotaxis in One Droplet of Blood Using Microfluidic Assays
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    Chapter 26 Leukocyte Migration and Deformation in Collagen Gels and Microfabricated Constrictions
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    Chapter 27 Microfluidic Devices for Examining the Physical Limits of Migration in Confined Environments
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    Chapter 28 Controlling Confinement and Topology to Study Collective Cell Behaviors
Attention for Chapter 2: Directional Collective Migration in Wound Healing Assays
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Chapter title
Directional Collective Migration in Wound Healing Assays
Chapter number 2
Book title
Cell Migration
Published in
Methods in molecular biology, March 2018
DOI 10.1007/978-1-4939-7701-7_2
Pubmed ID
Book ISBNs
978-1-4939-7700-0, 978-1-4939-7701-7
Authors

Nicolas Molinie, Alexis Gautreau

Abstract

Cell migration is suppressed by confluence in a process called contact inhibition. Relieving contact inhibition upon scratching is one of the simplest ways to induce cell migration in a variety of cell types. Wound healing is probably most relevant to epithelial monolayers, because epithelial cells generally assume a barrier function, which must be restored as fast as possible by the healing process. This versatile assay, however, can also be applied to fibroblasts and to tumor cell types. Furthermore, assessing the cell response to scratch wounding requires no special equipment or reagents. It is one of the few cell migration assays, which can even be performed without videomicroscopy, since the closure of the wound can be estimated at fixed time points. Several hours after wounding, directional collective migration is easily assessed and quantified. However, cell proliferation, which is also induced by the relief of contact inhibition, is one of the confounding factors of wound healing assays that must be taken into account. A recent alternative to the scratch-induced wound is to use special inserts to seed cells into closely spaced chambers. When the insert is removed, contact inhibition is relieved, similar to the scratch-induced wound. In this chapter, we provide the protocol of the two methods and compare their advantages and disadvantages. We also provide a protocol to estimate cell proliferation upon wound healing based on the incorporation of the nucleotide analog EdU.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 55 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 55 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 8 15%
Researcher 7 13%
Student > Bachelor 6 11%
Student > Ph. D. Student 4 7%
Other 3 5%
Other 8 15%
Unknown 19 35%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 13 24%
Agricultural and Biological Sciences 5 9%
Medicine and Dentistry 4 7%
Physics and Astronomy 3 5%
Nursing and Health Professions 3 5%
Other 7 13%
Unknown 20 36%