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First published online July 10, 2009
doi: 10.1242/10.1242/dev.036517



1 Université de Toulouse, UPS, Centre de Biologie du
Développement, Bâtiment 4R3, 118 route de Narbonne, F-31062
Toulouse, France.
2 University of Bristol, Departments of Biochemistry and Physiology &
Pharmacology, Medical Sciences Building, University Walk, Bristol BS8 1TD,
UK.
3 CNRS, UMR5547, Centre de Biologie du Développement, F-31062 Toulouse,
France.
Authors for correspondence (e-mails:
payre{at}cict.fr;
plaza{at}cict.fr)
Accepted 28 May 2009
Fascin is well characterized in vitro as an actin-bundling protein and its increased expression is correlated with the invasiveness of various cancers. However, the actual roles and regulation of Fascin in vivo remain elusive. Here we show that Fascin is required for the invasive-like migration of blood cells in Drosophila embryos. Fascin expression is highly regulated during embryonic development and, within the blood lineage, is specific to the motile subpopulation of cells, which comprises macrophage-like plasmatocytes. We show that Fascin is required for plasmatocyte migration, both as these cells undergo developmental dispersal and during an inflammatory response to epithelial wounding. Live analyses further demonstrate that Fascin localizes to, and is essential for the assembly of, dynamic actin-rich microspikes within plasmatocyte lamellae that polarize towards the direction of migration. We show that a regulatory serine of Fascin identified from in vitro studies is not required for in vivo cell motility, but is crucial for the formation of actin bundles within epithelial bristles. Together, these results offer a first glimpse into the mechanisms regulating Fascin function during normal development, which might be relevant for understanding the impact of Fascin in cancers.
Key words: Drosophila, Fascin (Singed), Hemocytes, Migration, Wound healing
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