Placental labyrinth formation in mice requires endothelial FLRT2/UNC5B signaling

Development. 2017 Jul 1;144(13):2392-2401. doi: 10.1242/dev.149757. Epub 2017 Jun 2.


The placental labyrinth is the interface for gas and nutrient exchange between the embryo and the mother; hence its proper development is essential for embryogenesis. However, the molecular mechanism underlying development of the placental labyrinth, particularly in terms of its endothelial organization, is not well understood. Here, we determined that fibronectin leucine-rich transmembrane protein 2 (FLRT2), a repulsive ligand of the UNC5 receptor family for neurons, is unexpectedly expressed in endothelial cells specifically in the placental labyrinth. Mice lacking FLRT2 in endothelial cells exhibited embryonic lethality at mid-gestation, with systemic congestion and hypoxia. Although they lacked apparent deformities in the embryonic vasculature and heart, the placental labyrinths of these embryos exhibited aberrant alignment of endothelial cells, which disturbed the feto-maternal circulation. Interestingly, this vascular deformity was related to endothelial repulsion through binding to the UNC5B receptor. Our results suggest that the proper organization of the placental labyrinth depends on coordinated inter-endothelial repulsion, which prevents uncontrolled layering of the endothelium.

Keywords: Angiogenesis; FLRT2; Neurovascular; Placenta; UNC5B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Endothelial Cells / metabolism
  • Female
  • Gene Deletion
  • Hypoxia / pathology
  • Membrane Glycoproteins / deficiency
  • Membrane Glycoproteins / metabolism*
  • Mice, Inbred C57BL
  • Neovascularization, Physiologic
  • Netrin Receptors
  • Organogenesis*
  • Placenta / blood supply
  • Placenta / cytology
  • Placenta / embryology*
  • Placenta / metabolism*
  • Pregnancy
  • Receptors, Cell Surface / deficiency
  • Receptors, Cell Surface / metabolism
  • Signal Transduction*


  • FLRT2 protein, mouse
  • Membrane Glycoproteins
  • Netrin Receptors
  • Receptors, Cell Surface