Fig. 5

Impairments in photoreceptors, the retinal pigment epithelium (RPE), and ocular vasculature induced by GUCA1A p.R120L in zebrafish. (a–d) Immunofluorescent staining of rhodopsin (RHO) (red; a,b), peanut agglutinin (PNA) lectin (green; a,b), and Zpr-1 (red; c,d). RHO and PNA expressions were significantly reduced in zebrafish overexpressing GUCA1A^p.R120L (a,b). Zpr-1 expression was only slightly reduced in the GUCA1A^p.R120L-injected group (d) when compared with GUCA1A^WT-injected zebrafish (c). (e–g) Relative messenger RNA (mRNA) levels of photoreceptor-, cone-, and rod-specific transcripts in GUCA1A^p.R120L- and GUCA1A^WT+p.R120L-injected zebrafish compared with the GUCA1A^WT-injected group. (h–j) Robust Zpr-2 expression was detected in retinal frozen sections of 4-dpf larvae injected with GUCA1A^WT (h), whereas Zpr-2 expression was diminished in the GUCA1A^p.R120L-injected (i) and GUCA1A^WT+p.R120L-injected (j) groups. (k) Relative mRNA levels of RPE characteristic transcripts in the GUCA1A^p.R120L- and GUCA1A^WT+p.R120L-injected groups were decreased when compared with the GUCA1A^WT-injected zebrafish. (l) No truncal vascular anomaly is revealed in transgenic (flk1: enhanced green fluorescent protein (EGFP)) zebrafish injected with GUCA1A^p.R120L. (m) Axial projections of confocal images from the two injected groups. Fluorescent intensity of EGFP is significantly reduced in the GUCA1A^p.R120L-injected group. (n) The fluorescent intensity of EGFP calculated by ImageJ in the two groups. Results were obtained from technical triplicates. Error bars represent the SE. Error bars represent the SD. NS, not significant. *P < 0.05; **P < 0.01; ***P < 0.001. Scale bar = 20 mm.