Inhibition of cytotrophoblastic (JEG-3) cell invasion by interleukin 12 involves an interferon gamma-mediated pathway

J Biol Chem. 2004 Dec 31;279(53):55297-307. doi: 10.1074/jbc.M407013200. Epub 2004 Sep 23.

Abstract

Trophoblast invasion, like tumor invasion, shares common biochemical mechanisms. However, in contrast to tumor invasion of a host tissue, trophoblastic invasion during implantation is strictly regulated, temporospatially. Factors responsible for these important regulatory processes are presently unknown; however, studies indicate that cytokines and growth factors represent in the peri-implantation uterine milieu as the possible candidates. In this study we investigated the role of interleukin (IL) 12 in regulating trophoblast invasion and the expression of trophoblast proteases (matrix metalloprotease (MMP)-2, MMP-9, and urokinase-type plasminogen activators) and their inhibitors (tissue inhibitors of metalloprotease (TIMP) 1, TIMP-2, and plasminogen activator inhibitor (PAI)-1) using an in vitro tissue culture system of human choriocarcinoma cell line JEG-3. Our major findings show an anti-invasive role of IL-12, associated with an inhibitory effect on the proteases but with an opposite up-regulating influence on the protease inhibitor, TIMP-1, whereas TIMP-2 and plasminogen activator inhibitor 1 remained unaltered. Stimulation of JEG-3 cells with IL-12 also induced interferon (IFN)-gamma production, which when neutralized using a monoclonal anti-IFN-gamma antibody, F12, abrogates its ability to down-regulate the MMPs. IL-12 also mediates an IFN-gamma-dependent up-regulation of E-cadherin, thereby implying that alteration in cell-cell adhesion besides regulating the proteases and the inhibitors possibly contributes to the observed anti-invasive role of this cytokine. TIMP-1, although stimulated by IL-12, was found to be unaltered by antibody F12, thereby implying a possibility of an IL-12-dependent-IFN-gamma independent regulation. These findings thereby suggest an important role of IL-12 in modulation of trophoblast proteases and their inhibitors besides regulating cell-cell interactions and invasion during implantation, with far reaching possibilities for understanding the mechanism(s) and regulations of invasion and metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cadherins / metabolism
  • Cell Adhesion
  • Cell Line, Tumor
  • Cell Movement
  • Collagen / metabolism
  • Collagen / pharmacology
  • Cytokines / metabolism
  • Densitometry
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Drug Combinations
  • Embryo Implantation*
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Genes, Reporter
  • Genetic Vectors
  • Humans
  • Immunohistochemistry
  • Interferon-gamma / metabolism*
  • Interleukin-12 / metabolism*
  • Laminin / metabolism
  • Laminin / pharmacology
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Plasminogen Activator Inhibitor 1 / metabolism
  • Proteoglycans / metabolism
  • Proteoglycans / pharmacology
  • RNA / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Tissue Inhibitor of Metalloproteinase-1 / metabolism
  • Tissue Inhibitor of Metalloproteinase-2 / metabolism
  • Transfection
  • Trophoblasts / cytology*
  • Urokinase-Type Plasminogen Activator / metabolism

Substances

  • Cadherins
  • Cytokines
  • Drug Combinations
  • Laminin
  • Plasminogen Activator Inhibitor 1
  • Proteoglycans
  • Tissue Inhibitor of Metalloproteinase-1
  • matrigel
  • Tissue Inhibitor of Metalloproteinase-2
  • Interleukin-12
  • RNA
  • Interferon-gamma
  • Collagen
  • Urokinase-Type Plasminogen Activator
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9