Expression of macrophage inflammatory protein-3alpha in an endometrial epithelial cell line, HHUA, and cultured human endometrial stromal cells

Mol Hum Reprod. 2002 Oct;8(10):930-3. doi: 10.1093/molehr/8.10.930.

Abstract

It has been demonstrated that human endometrial epithelial cells (EEC) and stromal cells (ESC) produce a variety of chemokines in vivo and in vitro. To evaluate the expression of macrophage inflammatory protein (MIP)-3alpha in endometrial cells, the production of MIP-3alpha by an EEC line, HHUA, and cultured ESC stimulated with various inflammatory mediators was evaluated by ELISA. Unstimulated HHUA and ESC constitutively secreted MIP-3alpha. Tumour necrosis factor-alpha and interleukin-1beta significantly stimulated the secretion of MIP-3alpha by HHUA and ESC. Lipopolysaccharide also stimulated the secretion of MIP-3alpha by ESC, but not by HHUA. These results show that the concentration of MIP-3alpha in the endometrium is modulated by these inflammatory mediators. MIP-3alpha may contribute to the normal and pathological processes of human reproduction by regulating the trafficking of immature dendritic cells and memory T lymphocytes into the endometrium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cells, Cultured
  • Chemokine CCL20
  • Chemokines, CC / metabolism*
  • Culture Media / chemistry
  • Endometrium / cytology*
  • Endometrium / drug effects
  • Endometrium / metabolism*
  • Epithelial Cells / metabolism
  • Female
  • Humans
  • Interleukin-1 / metabolism
  • Interleukin-1 / pharmacology
  • Lipopolysaccharides / metabolism
  • Lipopolysaccharides / pharmacology
  • Macrophage Inflammatory Proteins / metabolism*
  • Receptors, CCR6
  • Receptors, Chemokine*
  • Stromal Cells / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • CCL20 protein, human
  • CCR6 protein, human
  • Chemokine CCL20
  • Chemokines, CC
  • Culture Media
  • Interleukin-1
  • Lipopolysaccharides
  • Macrophage Inflammatory Proteins
  • Receptors, CCR6
  • Receptors, Chemokine
  • Tumor Necrosis Factor-alpha