The G-Protein-Coupled Estrogen Receptor (GPER) is Expressed in Normal Human Ovaries and is Upregulated in Ovarian Endometriosis and Pelvic Inflammatory Disease Involving the Ovary

被引:36
作者
Heublein, Sabine [1 ]
Lenhard, Miriam [1 ]
Vrekoussis, Thomas [1 ]
Schoepfer, Jutta [2 ]
Kuhn, Christina [1 ]
Friese, Klaus [1 ]
Makrigiannakis, Antonis [3 ]
Mayr, Doris [4 ]
Jeschke, Udo [1 ]
机构
[1] Univ Munich, Dept Obstet & Gynaecol, D-80337 Munich, Germany
[2] Univ Munich, Dept Legal Med, D-80337 Munich, Germany
[3] Univ Crete, Sch Med, Dept Obstet & Gynaecol, Iraklion, Greece
[4] Univ Munich, Dept Pathol, D-80337 Munich, Germany
关键词
endometriosis; folliculogenesis; GPER; human ovary; BREAST-CANCER; GPR30; CELLS; CLONING; CYCLE;
D O I
10.1177/1933719112446085
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Estrogens play a crucial role in maintaining ovarian function. Deregulation of estrogen signals is associated with fertility-impairing disorders. The aim of this study was to investigate whether the G-protein-coupled estrogen receptor (GPER) is present in the human ovary. Additionally, we analyzed the folliculogenesis and ovarian endometriosis in GPER expression. Seventy-nine patients (ovarian endometriosis, n = 26; ovarian pelvic inflammatory disease [PID], n = 10; normal ovaries/endometrium, n = 30/13) were analyzed by immunohistochemistry. Normal ovaries were also assessed by real-time polymerase chain reaction and double immunofluorescence. The most intense expression of GPER was noted in the ovarian surface epithelium. Theca cells and oocytes were also significantly positive. Expression of GPER was more frequent in mature follicles/oocytes than in primordial ones, implying that GPER could be a selector during folliculogenesis. Moreover, GPER was upregulated in ovarian endometriosis and PID. Overexpression of GPER in both inflammation and endometriosis affecting the ovary may prove useful in explaining/predicting the main endometriosis-related symptoms.
引用
收藏
页码:1197 / 1204
页数:8
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