Vitamin A (retinol) and its active derivatives (retinoic acids) are essenti
al for growth and development of the mammalian fetus. Maternally derived re
tinol must pass the placenta to reach the developing fetus. Despite its app
arent importance, little is known concerning placental transfer and metabol
ism of retinol, and particularly of placental production and storage of ret
inyl esters, To elucidate this metabolic pathway, we incubated, in the pres
ence of retinol, 1) human full-term placental explants and 2) primary cultu
res of major cells types contributing to placental function: trophoblasts a
nd villous mesenchymal fibroblasts. We used HPLC to determine the types and
concentrations of retinyl eaters produced by these explants and cells. Abo
ut 14% of total cellular retinol in placental explants was esterified. The
most abundant esters were myristate and palmitate. Primary cell cultures sh
owed that fibroblasts efficiently produced retinyl esters, but trophoblasts
did not. In both types of experiments, no retinyl esters were detected in
the culture medium, suggesting that retinyl eaters were produced for storag
e purpose. These results suggest that villous mesenchymal fibroblasts are p
rimary sites of retinol esterification and storage in the placenta.