Macrophages and nerve fibres in peritoneal endometriosis

Hum Reprod. 2009 Apr;24(4):835-41. doi: 10.1093/humrep/den483. Epub 2009 Jan 9.

Abstract

Background: Endometriosis is considered to be an inflammatory disease, and macrophages are the most numerous immune cells in endometriotic lesions. However, the mechanisms underlying the elevation of macrophages and their role in the pathogenesis and manifestations of endometriosis still remain unclear.

Methods: The number of macrophages stained for CD68 in endometriotic lesions (n = 24) and in peritoneum distant from the lesions (n = 14) from women with endometriosis was compared with the number of macrophages in normal peritoneum from women without endometriosis (n = 18). Peritoneal lesions were also double-stained for CD68 and protein gene product 9.5 to study the relationship between macrophages and nerve fibres.

Results: The densities of macrophages in peritoneal endometriotic lesions and unaffected peritoneum from women with endometriosis were both significantly higher than that in normal peritoneum from women without endometriosis (P < 0.001). More nerve fibres were also found in the areas where increased numbers of macrophages were identified.

Conclusions: There was a significant elevation of macrophages in both normal peritoneum and peritoneal lesions from women with endometriosis compared with normal peritoneum from women without endometriosis. These cells may well play roles in the growth and development of endometriotic lesions and in the generation of pain through interaction with nerve fibres.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Cell Count
  • Endometriosis / etiology
  • Endometriosis / pathology*
  • Endometriosis / physiopathology
  • Female
  • Humans
  • Immunohistochemistry
  • Macrophages / pathology*
  • Macrophages / physiology
  • Nerve Fibers / pathology*
  • Nerve Fibers / physiology
  • Pain / physiopathology
  • Peritoneal Diseases / etiology
  • Peritoneal Diseases / pathology*
  • Peritoneal Diseases / physiopathology
  • Ubiquitin Thiolesterase / metabolism

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • UCHL1 protein, human
  • Ubiquitin Thiolesterase