Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/87493
Citations
Scopus Web of Science® Altmetric
?
?
Type: Book chapter
Title: Imaging pluripotent cell migration in drosophila
Author: Murray, M.
Saint, R.
Citation: Stem Cell Migration, 2011 / Filippi, M., Geiger, H. (ed./s), vol.750, Ch.12, pp.169-184
Publisher: Humana Press
Publisher Place: USA
Issue Date: 2011
Series/Report no.: Methods in Molecular Biology; 750
ISBN: 9781617791444
Editor: Filippi, M.
Geiger, H.
Statement of
Responsibility: 
Michael J. Murray and Robert Saint
Abstract: Drosophila melanogaster offers a powerful system for the analysis of cell migration. In the embryo, ­pluripotent cells of the mesodermal and endodermal primordia undergo epithelial–mesenchymal transitions and cell migration, while primordial germ cells migrate through an endodermal barrier to form the gonads. Visualisation of these migrations has traditionally been achieved by staining fixed embryos at different developmental stages or through live imaging of cells using tissue-specific expression of marker fluorescent proteins. More recently, photoactivatable fluorescence proteins have allowed the labelling of small groups of cells or single cells so that their migratory patterns and fate can be followed. By fusing the photoactivatable fluorescent protein to proteins that mark different subcellular components, it is now possible to visualise different aspects of the cells as they migrate. Here, we review previous studies of the migration of pluripotent embryonic cells and describe, in detail, methods for visualising these cells.
Keywords: Drosophila; Mesoderm; Photoactivatable GFP; Cell migration; Cell fate mapping
Rights: © Springer Science+Business Media, LLC 2011
DOI: 10.1007/978-1-61779-145-1_12
Published version: http://dx.doi.org/10.1007/978-1-61779-145-1_12
Appears in Collections:Aurora harvest 2
Molecular and Biomedical Science publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.