ZFIN Image: Yokota et al., 2015, Fig. 10

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Figure Caption

Fig. 10

Dll4 is involved in the selection of single stalk cells.

(A) The number of Ca²⁺-oscillating ECs following tip cells in each ISV of uninjected, or control MO- or dll4 MO-injected Tg(fli1:Gal4FF);(UAS:GCaMP7a);(fli1:H2B-mC) embryos during stalk cell budding when an EC/ECs following a tip cell is/are budding from the DA. Graph shows the occurrence rate of the indicated numbers of Ca²⁺-oscillating cells in each ISV among the total number of ISVs observed (indicated at the top). (B) 3D-rendered time-sequential images of Tg(fli1:Gal4FF);(UAS:GCaMP7a);(fli1:H2B-mC) embryos during stalk cell budding from the DA injected with dll4 MO (25 ss). A green arrowhead indicates tip cell. Orange and red arrowheads indicate budding stalk cells following tip cell. (C) The fluorescence changes in GCaMP7a (ΔF/F₀) of individual ECs from B indicated by arrowheads at the left panel are shown as a graph. (D) Ca²⁺ oscillation frequency (left) and mean ΔF/F₀ (right) in tip cells, stalk cells, and other ECs within the DA in dll4 morphants during stalk cell budding (n ≥ 10). As illustrated at the left panel, we designated budding ECs that follow tip cells as stalk cells. Scale bar, 10 mm in B. ***p < 0.001; NS, not significant. DA, dorsal aorta.

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Acknowledgments

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