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Spatiotemporal characterization of dynamic epithelial filopodia during zebrafish epiboly
Author(s) -
Rutherford Nathan E.,
Wong Alexander H.,
Bruce Ashley E. E.
Publication year - 2019
Publication title -
developmental dynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.634
H-Index - 141
eISSN - 1097-0177
pISSN - 1058-8388
DOI - 10.1002/dvdy.94
Subject(s) - epiboly , filopodia , blastoderm , biology , zebrafish , microbiology and biotechnology , gastrulation , polarity in embryogenesis , cell migration , actin , cell , embryo , embryogenesis , genetics , gene
Background During zebrafish epiboly, the embryonic cell mass, or blastoderm, spreads to enclose the yolk cell. The blastoderm consists of an outer epithelial sheet, the enveloping layer (EVL), and the underlying deep cell layer (DEL). Studies have provided insights into the mechanisms of EVL and deep cell epiboly, but little is known about the interactions between the two cell layers and what role they may play during epiboly. Results We used live imaging to examine EVL basal protrusions. We identified them as filopodia based on f‐actin content and localization of fluorescently tagged filopodial markers. A spatiotemporal analysis revealed that the largest number of EVL filopodia were present during early epiboly at the animal pole. In functional studies, expression of a constitutively active actin‐bundling protein resulted in increased filopodial length and delayed gastrulation. Conclusions We identified protrusions on the basal surface of EVL cells as filopodia and showed that they are present throughout the EVL during epiboly. The largest number of filopodia was at the animal pole during early epiboly, which is when and where deep cell radial intercalations occur to the greatest extent. These findings suggest that EVL filopodia may function during epiboly to promote deep cell rearrangements during epiboly initiation.