Fig. 4

Fig. 4

Phenotype evaluation and renal protein loss determination after induction of HPS1^KD, HPS3^KD, HPS4^KD and HPS5^KD in zebrafish. (A) The larval phenotype was analyzed at 96 hpf following HPS^KD at the 1–2 cell stage. Both HPS1^{KD i6e7} and HPS1^{KD ATG} larvae showed pericardial effusion and yolk sac edema and a slight curvature of the tail. HPS3^{KD e7i7} and similarly HPS3^{KD ATG} embryos revealed mild pericardial effusion without yolk sac edema and a straight tail. A similar effect of the knockdown was detected in both the HPS4^{KD e8i8} and HPS4^{KD ATG} groups which showed no pericardial effusion, yolk sac edema while a straight tail occurred. The HPS5^{KD e12i12} led to the most severe pericardial effusion, yolk sac edema and tail curvature, and the HPS5^{KD ATG} caused a milder degree of pericardial effusion, yolk sac edema but a tail curvature, while CTRL-MO injected larvae showed no signs of an abnormal phenotype. Scale bar = 500 µm. (B) Phenotypic changes, indicating glomerular filtration barrier impairment, were determined by grading each larva at 96 hpf in terms of severity of pericardial effusion and yolk sac edema. Applying this grading system, a physiological appearance was scored as a P1 while the most severe edema and pericardial effusion was scored as P4. The number of dead larvae at 96 hpf is also stated. Both HPS1^{KD i6e7} and HPS1^{KD ATG} resulted in either death or aberrance from the normal P1 condition in more than 50%, while a P2 phenotype in HPS1^{KD i6e7} and the P1 was in HPS5^{KD ATG} were the most prominent. HPS3^{KD e7i7} did not show phenotypic changes in comparison with the control group, while the HPS3^{KD ATG} showed a higher death rate but only mild to severe aberration in a minority of the larvae in comparison with the control group. In both HPS3^{KD e7i7} and HPS3^{KD ATG} larvae, a P1 phenotype was the most common. The HPS4^{KD e8i8} induced a higher death rate but only mild aberration in some larvae from the normal phenotype in comparison with the control group. The HPS4^{KD ATG} showed a similar death rate compared to the control while only the minority of larvae displayed a varying degree of aberration. HPS5^{KD e12i12} resulted in either death or deviated from the normal P1 condition in more than 50% of the cases, the P3 was in HPS5^{KD e12i12} the most prominent phenotype. The HPS5^{KD ATG} showed overall similar results as the control group. (C) Quantification of maximum fluorescence intensity in the retinal vessel plexus of a Tg(l-fabp:eGFP-DBP) transgene zebrafish line depicted in arbitrary units (AU). Scatterplot presenting maximum fluorescence intensity of the fish eye was analyzed with ImageJ. All HPS^KD groups were compared with the CTRL-MO injected group. HPS1^{KD i6e7}, HPS1^{KD ATG}, HPS5^{KD e12i12} and HPS5^{KD ATG} led to a decrease of fluorescence intensity, while HPS3^{KD e7i7}, HPS3^{KD ATG}, HPS4^{KD e8i8} and HPS4^{KD ATG} did not induce a reduction of fluorescence intensity. At least 26 animals were measured for each condition. The error bars indicate the mean ± SEM. n.s. = p ≥ 0.05, ***p ≤ 0.001, ****p ≤ 0.0001 by one-way ANOVA followed by Tukey’s multiple comparisons test.