4.7 Article Proceedings Paper

Reduced expression of progesteron receptor-B in the endometrium of women with endometriosis and in cocultures of endometrial cells exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin

期刊

FERTILITY AND STERILITY
卷 84, 期 1, 页码 67-74

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2005.01.113

关键词

progesterone receptor; endometrium; endometriosis; TCDD; MMFs

资金

  1. NICHD NIH HHS [U54 HD37321] Funding Source: Medline
  2. NIEHS NIH HHS [R21ES12298] Funding Source: Medline

向作者/读者索取更多资源

Objective: To analyze endometrial progesterone receptor (PR) expression in women with endometriosis compared with disease-free women and to assess the impact of in vitro 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure on PR isotype expression. Design: Controlled laboratory study. Setting: University medical center. Patient(s): Healthy volunteers and women with surgically diagnosed endometriosis. Intervention(s): None. Main Outcome Measure(s): Analysis of in vivo PR-A and PR-B expression in endometrium from women with and without endometriosis. The impact of in vitro TCDD exposure on PR-B/PR-A ratio and cell-specific matrix metalloproteinase, (MMP) expression was also determined. Result(s): The PR-B/PR-A ratio was lower in endometrial tissues from women with endometriosis compared with normal tissues. A similar ratio was induced in normal stromal cells cocultured with epithelial cells and exposed to TCDD. Disruption of stromal PR expression following TCDD exposure was associated with a failure of P-mediated down-regulation of both stromal-specific pro-MMP-3 and epithelial-specific pro-MMP-7. Conclusion(s): Our data suggest that reduced progesterone (P) sensitivity in the endometrium of women with endometriosis may be related to an altered pattern of PR expression. The ability of TCDD to selectively down-regulate stromal PR-B expression and increase MMP expression in both stromal and epithelial cells suggests that exposure to this toxin may negatively impact P-mediated cell-cell communication in the human endometrium. (c) 2005 by American Society for Reproductive Medicine.

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