Increased expression of macrophage colony-stimulating factor and its receptor in patients with endometriosis

Fertil Steril. 2012 May;97(5):1129-35.e1. doi: 10.1016/j.fertnstert.2012.02.007. Epub 2012 Feb 24.

Abstract

Objective: To investigate the expression and regulation of colony-stimulating factor 1 (CSF-1) and its receptor, C-FMS, in endometriosis.

Design: In vivo and vitro study.

Setting: University-based academic medical center.

Patient(s): Reproductive-age women undergoing surgery for benign conditions.

Intervention(s): Peritoneal and endometrial tissue samples were obtained.

Main outcome measure(s): CSF-1 and C-FMS expression.

Result(s): Significantly higher CSF-1 levels were found in peritoneal fluid of patients with endometriosis compared with control subjects. Ectopic endometriotic tissue had 3.5-fold and 1.7-fold increases in CSF-1 and C-FMS expression, respectively, compared with eutopic tissue. Coculture of endometrial cells from either established cell lines or patient samples with peritoneal mesothelial cells (PMCs) led to increased expression of CSF-1 and C-FMS. A higher but nonsignificant increase in levels of C-FMS and CSF-1 was found in cocultures of endometrial epithelial cells from patients with endometriosis compared with those without endometriosis.

Conclusion(s): Increased CSF-1 levels may contribute to endometriosis lesion formation and progression. Elevation in CSF-1 after coculture of endometrial cells with PMCs suggests that endometrial tissue may be a source of peritoneal CSF-1. Increased C-FMS expression in endometrial cells from women with endometriosis cocultured with PMCs suggests that endometrial tissue involved in lesion formation is highly responsive to CSF-1 signaling.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Academic Medical Centers
  • Ascitic Fluid / immunology
  • Cell Communication
  • Cells, Cultured
  • Coculture Techniques
  • Endometriosis / genetics
  • Endometriosis / immunology*
  • Endometriosis / pathology
  • Endometrium / immunology*
  • Endometrium / pathology
  • Epithelial Cells / immunology
  • Epithelial Cells / pathology
  • Female
  • Humans
  • Macrophage Colony-Stimulating Factor / genetics
  • Macrophage Colony-Stimulating Factor / metabolism*
  • Peritoneum / immunology
  • Peritoneum / pathology
  • Receptor, Macrophage Colony-Stimulating Factor / genetics
  • Receptor, Macrophage Colony-Stimulating Factor / metabolism*
  • Stromal Cells / immunology
  • Stromal Cells / pathology
  • Texas
  • Up-Regulation

Substances

  • Macrophage Colony-Stimulating Factor
  • Receptor, Macrophage Colony-Stimulating Factor