Extracellular matrix composition and hypoxia regulate the expression of HLA-G and integrins in a human trophoblast cell line

Biol Reprod. 2000 Mar;62(3):739-47. doi: 10.1095/biolreprod62.3.739.

Abstract

During human placentation, extravillous cytotrophoblast cells emerge from chorionic villi contacting the decidua to invade the uterine wall. When isolated from first-trimester placentae, cytotrophoblast cells undergo step-wise differentiation in vitro that recapitulates the phenotypic heterogeneity observed in vivo. We examined a cell line, HTR-8/SVneo, that has been established from human first-trimester cytotrophoblast to determine whether these cells possess some of the unique cytotrophoblast characteristics that have been described previously. Exposure during serum-free culture to hypoxic conditions (2% oxygen concentration) increased HTR-8/SVneo cell proliferation and reduced invasion of a three-dimensional basement membrane (Matrigel). During culture on surfaces coated with individual extracellular matrix proteins, HTR-8/SVneo cells expressed cytokeratin but not the trophoblast-specific major histocompatibility protein, HLA-G. However, HLA-G expression was induced in HTR-8/SVneo cells that contacted Matrigel. Expression of the alpha5 integrin subunit was relatively unaffected by matrix composition, whereas alpha1 was up-regulated and alpha6 was down-regulated after transferring cells to Matrigel. Hypoxia increased alpha6 and decreased both alpha1 and HLA-G expression on Matrigel. HTR-8/SVneo cells retain several important characteristics associated with primary cultures of first-trimester human cytotrophoblast cells, including their altered behavior in response to a changing maternal environment.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, CD / metabolism
  • Cell Division
  • Cell Hypoxia
  • Cell Line
  • Choriocarcinoma / metabolism
  • Choriocarcinoma / pathology
  • Endometrial Neoplasms / metabolism
  • Endometrial Neoplasms / pathology
  • Extracellular Matrix / chemistry
  • Extracellular Matrix / metabolism*
  • Female
  • HLA Antigens / metabolism*
  • HLA-G Antigens
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Integrin alpha1
  • Integrins / metabolism*
  • Ki-67 Antigen / metabolism
  • Pregnancy
  • Trophoblasts / metabolism*
  • Trophoblasts / pathology

Substances

  • Antigens, CD
  • HLA Antigens
  • HLA-G Antigens
  • Histocompatibility Antigens Class I
  • Integrin alpha1
  • Integrins
  • Ki-67 Antigen