FIGURE

Fig. S2

ID
ZDB-FIG-180129-13
Publication
Giger et al., 2017 - Endodermal germ-layer formation through active actin-driven migration triggered by N-cadherin
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Fig. S2

Endodermal cell internalization is independent of E-cadherin levels. (A) E-cadherin expression, assessed by immunohistochemistry, was reduced upon morpholino injection (animal views). Images were all acquired in the same conditions. (Scale bar: 20 µm.) Fluorescence intensity was quantified at cell boundaries (n = 6 embryos for each condition). ***P < 0.001. (B) To assess the importance of E-cadherin adhesion in internalization, endodermal cells were transplanted to the animal pole, E-cadherin being down-regulated either in transplanted endodermal cells or in their ectodermal neighbors. (Top) Sagittal sections showing the position of transplanted cells at midgastrulation. (Scale bar: 10 µm.) (Middle and Bottom) Distribution of embryos according to the percentage of internalized cells at midgastrulation plotted as histograms (Middle) or as a cumulative plot (Bottom). (C) E-cadherin expression assessed by immunohistochemistry in induced endodermal cells (expressing GFP) and ectodermal cells (animal view). Fluorescence intensity was quantified at boundaries between ectodermal cells and between endodermal cells (n = 5 embryos, P = 0.6). (Scale bar: 20 µm.) ns, nonsignificant (P > 0.05).

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Proc. Natl. Acad. Sci. USA