Fig. 5. Extra-embryonic expression of LPP3 partially rescues the placental
phenotype and reveals abnormal allantoic vasculogenesis. (A)
Rosa26
LPP3-/- chimeric embryo recovered at
E10.5. In the presence of wild-type extra-embryonic tissue (blue), the
allantois from this embryo, entirely derived from LPP3-/-
cells, contacted the chorion (arrow). The embryo is also developmentally
delayed. (B) Rosa26
LPP3-/- chimeric embryo
recovered at E10.5. This embryo, formed by a mixture of wild-type (blue) and
mutant cells showed more advanced development. Compare with the size and stage
of development of the littermate embryo shown in A. The allantois also
contacted the chorion (not shown). (C) Transverse section through the
chorio-allantoic region of the embryo shown in A. The section corresponded to
the maximum diameter of the chorioallantoic region. Although
LPP-/- mutant cells (pink) contacted the chorion
(arrowheads), the allantois remained as a compact mass of tissue that did not
invade the chorion. (D) Transverse section through the chorio-allantoic region
of the mixed chimera shown in B. Chorioallantoic placental development was
enhanced in the presence of a mixed population of LPP+/+
(blue) and LPP-/- cells. Chorionic development was
enhanced, as shown by the wavy appearance of the chorion (arrowheads),
increased diameter of the placenta and the formation of large allantoic blood
vessels (arrow). Note that the endothelial cells from the umbilical cord
vessels were predominantly of wild-type genotype (inset, blue cells). (E)
Allantois from a 5-somite wild-type embryo cultured for 36 hours. Note that
the PECAM1 positive endothelial cells (brown) developed a flat network of thin
capillary-like structures. (F) Allantois from a 5-somite
LPP3-/- embryo treated as in E. A mass of PECAM1-positive
endothelial cells remained in the center of the explant.