Fig. S8
- ID
- ZDB-IMAGE-160516-14
- Publication
- Ando et al., 2016 - Clarification of mural cell coverage of vascular endothelial cells by live imaging of zebrafish
- All Figures
- Figures for Ando et al., 2016
Fig. S8
Investigation of the origin of MCs in the hyaloid vessels and the vessels in the pharyngeal region. (A) Confocal images of hyaloid vessels in the 3 dpfTgBAC(pdgfrb:EGFP);Tg(fli1a:Myr-mCherry) larvae injected with control MO (upper panels in A and B)or either both foxd3 and tfap2a MOs (lower panel in A) or both tbx6 and hand2 MOs (lower panel in B). Lateral view, anterior to the left. Left, pdgfrb:EGFP; center, the merged images of pdgfrb:EGFP (green) and fli1a:Myr-mCherry(red); right, fli1a:Myr-mCherry. (C, D) Confocal images of vessels in the pharyngeal region in the 4 dpfTgBAC(pdgfrb:EGFP);Tg(fli1a:Myr-mCherry) larvae injected with control MO(left columns in C and D) or eitherboth foxd3 and tfap2a MOs (right column in C) or foxd3 MO (right column in D). Top, pdgfrb:EGFP; middle, the merged images of pdgfrb:EGFP (green) and fli1a:Myr-mCherry(red); bottom, fli1a:Myr-mCherry.In D, the boxed areas are enlarged to the right. Note that foxd3/tfap2a-double morphant larva exhibited severe structural defects in the head, although it could form abnormal HA. AA, aortic arches; HA, hypobranchial artery.Scale bars, 20 µm (enlarged image in D) or 50 µm (A-E).