Interferon-gamma receptors on human gestational choriocarcinoma cell lines: quantitative and functional studies

Am J Obstet Gynecol. 1992 Aug;167(2):524-30. doi: 10.1016/s0002-9378(11)91448-3.

Abstract

Objectives: This study was performed to further define the effects of interferon-gamma on choriocarcinoma cell lines and to determine whether variations in response among cell lines are attributable to quantitative differences in interferon-gamma receptors.

Study design: Interferon-gamma receptors were quantified on BeWo, JEG-3 and Jar choriocarcinoma cell lines by a radiolabeled interferon-gamma ligand binding assay. The response of these cell lines to interferon-gamma was measured in two functional assays: a cell proliferation assay and a cell lysis assay after exposure to interferon-gamma with and without actinomycin-D.

Results: The number of interferon-gamma receptors on BeWo, Jar, and JEG-3 cells did not differ significantly (650, 560, and 420 interferon-gamma receptors per cell, respectively). Proliferation of all three choriocarcinoma cell lines was significantly inhibited to a similar extent by interferon-gamma. After treatment with interferon-gamma actinomycin-D, each choriocarcinoma cell line exhibited dose-dependent cell lysis; lysis of Jar was significantly less than that of either BeWo or JEG-3.

Conclusion: These data further document variations in the response of choriocarcinoma cell lines to interferon-gamma and indicate that these differences are not the result of interferon-gamma receptor number but of postreceptor mechanisms.

Publication types

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

MeSH terms

  • Binding Sites
  • Binding, Competitive
  • Cell Division / drug effects
  • Choriocarcinoma / metabolism*
  • Choriocarcinoma / pathology
  • Female
  • Humans
  • Pregnancy
  • Pregnancy Complications, Neoplastic / metabolism*
  • Pregnancy Complications, Neoplastic / pathology
  • Receptors, Immunologic / metabolism*
  • Receptors, Interferon
  • Tumor Cells, Cultured

Substances

  • Receptors, Immunologic
  • Receptors, Interferon