Direct involvement of HERV-W Env glycoprotein in human trophoblast cell fusion and differentiation

Mol Cell Biol. 2003 May;23(10):3566-74. doi: 10.1128/MCB.23.10.3566-3574.2003.

Abstract

We recently demonstrated that the product of the HERV-W env gene, a retroviral envelope protein also dubbed syncytin, is a highly fusogenic membrane glycoprotein inducing the formation of syncytia on interaction with the type D mammalian retrovirus receptor. In addition, the detection of HERV-W Env protein (Env-W) expression in placental tissue sections led us to propose a role for this fusogenic glycoprotein in placenta formation. To evaluate this hypothesis, we analyzed the involvement of Env-W in the differentiation of primary cultures of human villous cytotrophoblasts that spontaneously differentiate by cell fusion into syncytiotrophoblasts in vitro. First, we observed that HERV-W env mRNA and glycoprotein expression are colinear with primary cytotrophoblast differentiation and with expression of human chorionic gonadotropin (hCG), a marker of syncytiotrophoblast formation. Second, we observed that in vitro stimulation of trophoblast cell fusion and differentiation by cyclic AMP is also associated with a concomitant increase in HERV-W env and hCG mRNA and protein expression. Finally, by using specific antisense oligonucleotides, we demonstrated that inhibition of Env-W protein expression leads to a decrease of trophoblast fusion and differentiation, with the secretion of hCG in culture medium of antisense oligonucleotide-treated cells being decreased by fivefold. Taken together, these results strongly support a direct role for Env-W in human trophoblast cell fusion and differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation
  • Cell Fusion
  • Endogenous Retroviruses / metabolism*
  • Gene Products, env / genetics*
  • Giant Cells / metabolism
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Oligonucleotides / chemistry
  • Oligonucleotides, Antisense / pharmacology
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • Time Factors
  • Trophoblasts / metabolism*

Substances

  • Gene Products, env
  • Oligonucleotides
  • Oligonucleotides, Antisense
  • RNA, Messenger
  • RNA