E-cadherin, as a negative regulator of invasive behavior of human trophoblast cells, is down-regulated by cyclosporin A via epidermal growth factor/extracellular signal-regulated protein kinase signaling pathway

Biol Reprod. 2010 Sep;83(3):370-6. doi: 10.1095/biolreprod.110.083402. Epub 2010 Apr 28.

Abstract

Our previous study has demonstrated cyclosporin A (CsA) promotes the invasiveness of human first-trimester trophoblast cells. In the present study, we further investigated the intracellular signaling pathway responsible for the improvements in CsA-induced invasiveness of human trophoblast cells. We showed that CsA down-regulated E-cadherin transcription and translation in human primary cultured trophoblast cells and choriocarcinoma cell line JEG-3. U0126, an inhibitor of extracellular signal-regulated protein kinase (ERK), attenuated the CsA-induced transcriptional repressor SNAI2 (also called Slug) expression and restored E-cadherin expression inhibited by CsA in JEG-3 cells. We further demonstrated that CsA amplified epidermal growth factor (EGF)-stimulated EGF receptor (EGFR) tyrosine phosphorylation in JEG-3 cells, and inhibition of EGFR tyrosine phosphorylation by AG1478, an EGFR tyrosine kinase inhibitor, abolished the down-regulation of E-cadherin by CsA through ERK signaling pathway. Moreover, our data showed that E-cadherin expression was negatively correlated to the invasiveness of JEG-3 cells, and CsA could reverse the decreased invasiveness of JEG-3 cells that resulted from E-cadherin overexpression. In conclusion, these observations indicate that CsA may decrease E-cadherin expression via EGFR/ERK signaling pathway and, ultimately, contribute to the invasiveness improvement of human trophoblast cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Blotting, Western
  • Cadherins / metabolism*
  • Cell Adhesion / drug effects
  • Cell Line, Tumor
  • Cells, Cultured
  • Cyclosporine / metabolism*
  • Cyclosporine / pharmacology
  • Down-Regulation / drug effects*
  • Epidermal Growth Factor / metabolism*
  • ErbB Receptors / metabolism
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Female
  • Fluorescent Antibody Technique
  • Humans
  • Immunoprecipitation
  • Phosphorylation / drug effects
  • Pregnancy
  • RNA, Small Interfering
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / drug effects*
  • Transcription, Genetic / drug effects
  • Transfection
  • Trophoblasts / cytology
  • Trophoblasts / drug effects
  • Trophoblasts / metabolism*

Substances

  • Cadherins
  • RNA, Small Interfering
  • Epidermal Growth Factor
  • Cyclosporine
  • ErbB Receptors
  • Extracellular Signal-Regulated MAP Kinases