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Effect of CAV-1 on Aibp2-regulated LEC specification. a Representative TEM images of control and cav1−/− zebrafish. Arrows show typical caveolae in cardinal vein ECs. b Quantification of caveolae in a. n = 27 (control) and n = 20 (cav1−/−) cells. c Maxi-projection confocal images of Prox1+ cells in the 36 hpf apoa1bp−/−; fli1a:egfp zebrafish with cav-1 crRNA alone or cav1-crRNA and Cas12a protein co-administration. Arrows show the Prox1+ LECs in cardinal vein. Green marks blood vessels, and red marks Prox1 staining. d Quantitative data of Prox1+ LECs in cardinal vein (7 somites) of (c). n = 34 embryos in both groups. e Representative confocal images of LEC specification in the cardinal veins of Vegfr3AAA knock-in zebrafish at 36 hpf. Green marks blood vessels, and red marks Prox1+ cells. f Quantitative data of LEC numbers in (e). n = 13 (flt4+/+) and n = 11 (flt4+/AAA) embryos. g Confocal imaging of Prox1+ LECs in the indicated genetically modified fli1a:egfp zebrafish at 36 hpf. Green marks blood vessels, and red marks Prox1 staining. h Quantitative data of Prox1+ LECs of 7 somites in (g). n = 22 (apoa1bp−/−; flt4+/+) and n = 26 (apoa1bp−/−; flt4+/AAA) embryos. Mean ± SE in b, d, f, and h; unpaired two-sided t-test with Welch’s correction. CV cardinal vein. Scale bar: 500 nm in a; 50 µm in c, e, g. Source data are provided as a Source Data file.
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