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. 2013 Jul 9;8(7):e68033. doi: 10.1371/journal.pone.0068033

Figure 4. Tumor angiogenesis is abolished in PKD1 morphant tg(fli1:EGFP) zebrafish embryos.

Figure 4

A–A″, Overall morphology of Co-Mo - injected (2 ng) or PKD1 SB-Mo I5 - injected (500 pg) 96 hpf embryos. At 48 hpf 1–4 nl of Matrigel (A, B) or Matrigel/HCT116 solution (A′, A″, B′, B″) was injected in the perivitelline space. Red boxes indicate regions of pictures shown in (B–B″). B–B″, HCT116 induced tumor angiogenesis as indicated by sprouting of subintestinal venous plexus (SIV) was analyzed at 96 hpf in tg(fli1:EGFP) embryos. Injection of HCT116 tumor cells (labeled with VybrantDil in red, arrow) led to a strong formation of ectopic blood vessels originated from the SIV (asterisks). In PKD1 morphants ectopic blood vessel formation was completely blocked. C–C′, Quantification of sprouting length per embryo (C) and cumulative sprouting length (C′) with S.D. of at least 30 embryos per group. For cumulative sprouting-length all sprouts of the same number of embryos per group were summed, (C′) represents means of three independent experiments with S.D. Black scale bars: 300 µm; white scale bars: 100 µm. *P<0.05, **P<0.01, ***P<0.001.