Author/Authors :
P. M. Coan، نويسنده , , A. C. Ferguson-Smith and G. J. Burton، نويسنده ,
Abstract :
The mouse is an extremely useful experimental model for the study of human disease owing to the ease of genetic
and physiological manipulation. A more detailed knowledge of murine placental development will, we hope,
increase our understanding of the pathogenesis of placentally related complications of human pregnancy. The
murine placenta consists of two main fetally derived compartments: the labyrinthine zone and the junctional zone.
Exchange in the labyrinthine zone takes place across an interhaemal membrane comprising an outer layer of
cytotrophoblast cells and two inner layers of syncytial trophoblast. The cytotrophoblast layer thins as gestation
advances, and in addition becomes highly perforated after embryonic day (E)12.5. Furthermore, as gestation
advances cytotrophoblast nuclear volume and DNA content increase, suggesting the formation of labyrinthine
trophoblast giant cells. The syncytial layers become increasingly microvillous, enlarging the surface area for
exchange. Separate basement membranes support the syncytium and the fetal capillary endothelium throughout
gestation, although these appear to fuse where the capillaries are closely approximated to the trophoblast. The
junctional zone consists of two principal trophoblast cell types, spongiotrophoblasts and invasive glycogen cells,
yet the functions of each remain elusive. Spongiotrophoblasts vary in their appearance even when not fully differentiated,
but a striking feature is the extensive endoplasmic reticulum of the more mature cells. Early glycogen
cells are distinguished by the presence of electron-dense glycogen granules, and large amounts of surrounding
extracellular matrix. Later the accumulations of glycogen granules occupy almost all the cytoplasm and there are
few organelles. This is the first study to use both scanning and transmission electron microscopy in an ultrastructural
description of murine placental development and is complementary to contemporary genetic investigations.
Keywords :
mouse , development , trophoblast , electron microscopy