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. 2019 Jan 28;10:453. doi: 10.1038/s41467-019-08315-w

Fig. 3.

Fig. 3

Deletion of Smad4 specifically in arterial endothelial cells does not affect vascular patterning or early embryonic development. a, b Representative pan-endothelial Tie2:Cre;Smad4fl/+ and Tie2:Cre;Smad4fl/fl whole-mount images (a) and transverse sections (b) from E10.5 embryos also transgenic for the Cre-reporter Rosa26R:LacZ. The cardinal vein (cv) cannot be identified in the Smad4fl/fl embryo, although the dorsal aorta (da) can be seen in both. Grey scale bars are 500 μm, black scale bars are 100 μm. c, d Representative arterial-specific Dll4in3:Cre;Smad4fl/+ and Dll4in3:Cre;Smad4fl/fl whole-mount images (c) and transverse sections (d) from E10.5 embryos also transgenic for the Cre-reporter Rosa26R:LacZ. Arterial-specific deletion of Smad4 had no effect on vasculature development at E10.5. Grey scale bars are 500 μm, black scale bars are 100 μm. e Observed frequency of Smad4fl/fl;Dll4in3:Cre embryos from E9.5 to P5. Only two sick (*) P5 Smad4fl/fl;Dll4in3:Cre animals were recovered. EC indicates Tie2:Cre-mediated deletion, ART indicates Dll4in3:Cre-mediated deletion, da = dorsal aorta, nt = neural tube, cv = cardinal vein, ica = inner cerebral artery, isa = intersomitic arteries. See also Supplementary Figure 3