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Fig. 2. Severe liver hypoplasia in vHnf1-/- embryos.
(A) Direct observation of WT and vHnf1-/- mouse
embryos at E13.5 shows an essentially empty abdominal cavity in the mutants
(arrows). (B) Liver dissection at E14.5 reveals the liver hypoplasia of
mutant embryos. (C,D) Hematoxylin and Eosin (H&E) staining
of sagittal sections of WT (C) and vHnf1-/- (D) embryos at
E13.5 show the reduced volume of mutant liver and the presence of hemorrhagic
regions (arrow). At higher magnification, the strong disorganization of mutant
liver tissue is evident (compare insets). (E,F) Immunostaining
at E13.5 indicates the absence of E-cadherin expression in mutant liver (F),
in contrast to WT (E) in which the staining reveals the epithelial
organization of hepatoblasts. The insets illustrate correct E-cadherin
expression in the stomach epithelium of WT (E) and of mutant (F) embryos.
(G,H) TUNEL analysis at E13.5 shows a massive apoptosis of the
majority of cells that compose the mutant liver (H), whereas in WT embryos few
apoptotic cells are observed (G). The dashed line outlines the liver.