Expression of human β-defensin-2 in the eutopic and ectopic endometrial tissues in patients with endometriosis

Arch Gynecol Obstet. 2013 Jun;287(6):1151-7. doi: 10.1007/s00404-012-2686-7. Epub 2012 Dec 27.

Abstract

Objective: To investigate the expression of human β-defensin-2 (hBD-2) in the endometrium of patients with endometriosis (EMS) and explore the potential role of hBD-2 in the pathogenesis of EMS.

Design: Prospective controlled study.

Sample: 50 women including EMS patients undergoing laparoscopic ovarian cystectomy and non-EMS patients undergoing hysterectomy for uterine fibroids.

Setting: Large university teaching hospital.

Methods: Patients were divided into EMS and non-EMS groups. The gene expressions of hBD-2, interleukin (IL)-1β and tumor necrosis factor (TNF)-α in the endometrial tissues of each group were detected with real-time quantitative polymerase chain reaction (PCR), and hBD-2 protein expression with immunohistochemical method.

Results: The gene expression levels of hBD-2, TNF-α, and IL-1β as well as the positive expression rate of hBD-2 protein in the ectopic endometrium of EMS patients were significantly higher than those in the eutopic endometrium of EMS and non-EMS patients (all P < 0.05). Correlation analysis showed that the gene expression levels of hBD-2 in the ectopic and eutopic endometrium of EMS patients were positively correlated with the gene expression levels of IL-1β and TNF-α (P < 0.01).

Conclusion: High levels of hBD-2 gene and protein expressions in the ectopic endometrium of EMS patients may be an important contributor in the pathogenesis of EMS. TNF-α and IL-1β may promote the upregulation of hBD-2 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Endometriosis / metabolism*
  • Endometrium / chemistry*
  • Female
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Interleukin-1beta / genetics
  • Prospective Studies
  • RNA, Messenger / analysis
  • Real-Time Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / genetics
  • beta-Defensins / analysis*
  • beta-Defensins / genetics*

Substances

  • DEFB4A protein, human
  • Interleukin-1beta
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • beta-Defensins