Distribution of human endogenous retrovirus type W receptor in normal human villous placenta

Pathology. 2007 Aug;39(4):406-12. doi: 10.1080/00313020701444572.

Abstract

Background: The fusion of trophoblast cells into the villous syncytiotrophoblast is crucial for appropriate placental function and fetal development. Fusion occurs following the interaction of syncytin-1, an envelope protein of the endogenous retrovirus HERV-W, and the RD114/mammalian type D retrovirus receptor (RDR/ASCT2) on adjacent cell membranes. This process must be tightly regulated in order to maintain the proliferative pool of cytotrophoblast cells as well as the function of the syncytia.

Aim: We sought to investigate whether syncytial fusion of placental cytotrophoblast cells may be regulated via modulation of RDR/ASCT2 expression.

Methods: Expression of RDR/ASCT2 in term and first trimester villous placenta was assessed along with a number of molecular markers using immunofluorescent staining. In a complementary approach, Western blotting was used to investigate RDR/ASCT2 expression in a panel of choriocarcinoma cell lines before and after stimulation of fusion.

Results: Villous placental RDR/ASCT2 expression was found to be restricted to the cytotrophoblast compartment, being largely absent in the syncytiotrophoblast. Local variations in RDR/ASCT2 expression were not associated with the proliferative status of cytotrophoblast cells. RDR/ASCT2 expression was also shown to be down-regulated in BeWo choriocarcinoma cells after stimulation of syncytial fusion.

Conclusion: This first report of the localisation and distribution of RDR/ASCT2 in human placental villi suggests that the fusion of placental trophoblast cells is not regulated by local or temporal variations of RDR/ASCT2 expression in villous cytotrophoblast cells.

MeSH terms

  • Amino Acid Transport System ASC / metabolism*
  • Cell Line, Tumor
  • Choriocarcinoma / metabolism
  • Choriocarcinoma / pathology
  • Chorionic Villi / metabolism*
  • Chorionic Villi / pathology
  • Female
  • Humans
  • Minor Histocompatibility Antigens
  • Placenta / metabolism*
  • Placenta / pathology
  • Pregnancy
  • Trophoblasts / metabolism
  • Trophoblasts / pathology
  • Uterine Neoplasms / metabolism
  • Uterine Neoplasms / pathology

Substances

  • Amino Acid Transport System ASC
  • Minor Histocompatibility Antigens
  • SLC1A5 protein, human