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. 2020 Feb 25;61(2):39. doi: 10.1167/iovs.61.2.39

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Copyright 2020 The Authors

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Figure 4. — Progressive vascular pathology in znf408-mutant zebrafish larvae and adults. (a) Confocal micrographs at 5, 90, or 180 days postfertilization (dpf) of the hyaloid (5 dpf, top row) or retinal vessels (90 dpf, second row and 180 dpf, third row) in znf408^+/+, znf408^rmc105/+, znf408^{rmc105/rmc105}, znf408^{rmc103/rmc103}, and znf408^{rmc104/rmc104} zebrafish crossed onto the Tg(flk1:GFP) background (vessels shown in green) following injection with rhodamine-conjugated dextran (plasma shown in red). (b) Quantification of the number of hyaloid vessels at 5 dpf from the groups shown in (a). n = 10, ANOVA: P < 0.001, Dunnett's post hoc: ***P < 0.001. (c) Quantification of the number of sprouts in the retinal vessels at 90 dpf from the groups shown in (a). n = 10, ANOVA: P < 0.001, Dunnett's post hoc: ***P < 0.001. (d) Quantification of the leaked dextran as a percentage of total dextran in the retinal vasculature at 180 dpf from the groups shown in (a). n = 10, ANOVA: P < 0.001, Dunnett's post hoc: ***P < 0.001.