PUBLICATION

Imaging of Endothelial Cell Dynamic Behavior in Zebrafish

Authors
Coxam, B., Gerhardt, H.
ID
ZDB-PUB-180923-9
Date
2018
Source
Methods in molecular biology (Clifton, N.J.)   1846: 181-195 (Chapter)
Registered Authors
Coxam, Baptiste, Gerhardt, Holger
Keywords
Cell cycle, Endothelial cells, Kymograph, Membrane, Polarity, Spinning disk, Vasculature, Zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Biomarkers
  • Cell Cycle
  • Cell Membrane/metabolism
  • Cell Membrane/pathology
  • Embryo, Nonmammalian
  • Endothelial Cells/metabolism*
  • Fluorescent Antibody Technique
  • Genes, Reporter
  • Intercellular Junctions
  • Molecular Imaging*/methods
  • Zebrafish*
PubMed
30242760 Full text @ Meth. Mol. Biol.
Abstract
In recent years, use of the zebrafish embryo as a model organism to study vascular development in vivo has provided valuable insights into the genetic and cellular events shaping the embryonic vasculature. In this chapter, we aim to present the methods for the measurement of some of the most commonly investigated dynamic parameters in endothelial cells during developmental angiogenesis, namely, migration speed and acceleration, filopodia extension, front-rear polarity, cell cycle progression, membrane deformations, and junctional rearrangements. We also offer suggestions on how to deal with the most common imaging and quantifications challenges faced when acquiring and quantifying endothelial cell dynamic behavior in vivo.We intend this section to serve as an experience-based imaging primer for scientists interested in endothelial cell imaging in the zebrafish embryo.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping