Glucocorticoid signaling regulates cell invasion and migration in the human first-trimester trophoblast cell line Sw.71

Am J Reprod Immunol. 2018 Jul;80(1):e12974. doi: 10.1111/aji.12974. Epub 2018 May 18.

Abstract

Problem: The development of the placenta and its functions are sensitive to infection and stress, which can activate the hypothalamic-pituitary-adrenal axis. Adrenally produced glucocorticoids are the body's primary mediators of the inflammatory and stress response. Although the glucocorticoid receptor (GR) is expressed in all human villous trophoblast tissue, the effect of glucocorticoids on placentation is not well understood.

Method of study: Using microarray analysis, we identified the glucocorticoid-regulated transcriptional profile in the immortalized first-trimester extravillous trophoblast cell line Swan.71 (Sw.71).

Results: The synthetic glucocorticoid dexamethasone significantly regulated 3829 genes, including genes associated with cell movement, growth, and survival. SERPINE1, an inhibitor of trophoblast invasion, was induced by glucocorticoids in Sw.71 cells and is associated with the pathogenesis of preeclampsia. Glucocorticoid treatment induced recruitment of activated polymerase II and GR to the SERPINE1 promoter, suggesting a mechanism for transcriptional regulation. Functionally, glucocorticoid treatment inhibited cell proliferation, migration, and invasion.

Conclusion: These findings suggest that glucocorticoids regulate extravillous trophoblast functions by altering the gene expression profile, which may contribute to the pathogenesis of reproductive disorders such as preeclampsia and IUGR.

Keywords: gene regulation; glucocorticoids/glucocorticoid receptor; hormone action; immune response; placenta; trophoblast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cell Movement / drug effects*
  • Cell Movement / genetics
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Dexamethasone / pharmacology
  • Female
  • Glucocorticoids / metabolism*
  • Humans
  • Neoplasm Invasiveness / pathology*
  • Plasminogen Activator Inhibitor 1 / genetics
  • Pregnancy
  • Pregnancy Trimester, First / drug effects
  • Pregnancy Trimester, First / genetics
  • Pregnancy Trimester, First / metabolism*
  • Promoter Regions, Genetic / drug effects
  • Promoter Regions, Genetic / genetics
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Signal Transduction / physiology*
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / genetics
  • Trophoblasts / drug effects
  • Trophoblasts / metabolism*

Substances

  • Glucocorticoids
  • Plasminogen Activator Inhibitor 1
  • Dexamethasone