Wnts are secreted signaling molecules implicated in various developmental p
rocesses and frizzled proteins are the receptors for these Wnt ligands. To
investigate the physiological roles of frizzled proteins, we isolated and c
haracterized a novel mouse frizzled gene Fzd5, Fzd5 mRNA was expressed in t
he yolk sac, eye and lung bud at 9.5 days post coitum, Fzd5 specifically sy
nergized with Wnt2, Wnt5a and Wnt10b in ectopic axis induction assays in Xe
nopus embryos. Using homologous recombination in embryonic stem cells, we h
ave generated Fzd5 knockout mice. While the heterozygotes were viable, fert
ile and appeared normal, the homozygous embryos died in utero around 10.75
days post coitum, owing to defects in yolk sac angiogenesis. At 10.25 days
post coitum, prior to any morphological changes, endothelial cell prolifera
tion was markedly reduced in homozygous mutant yolk sacs, as measured by Br
dU labeling. By 10.75 days post coitum, large vitelline vessels were poorly
developed, and the capillary plexus was disorganized. At this stage, vascu
logenesis in the placenta was also defective, although that in the embryo p
roper was normal. Because Wnt5a and Wnt10b co-localized with Fzd5 in the de
veloping yolk sac, these two Wnts are likely physiological ligands for the
Fzd5-dependent signaling for endothelial growth in the yolk sac.