Stimulation of GPR30 Increases Release of EMMPRIN-Containing Microvesicles in Human Uterine Epithelial Cells

被引:26
作者
Burnett, Lindsey A. [1 ]
Light, Mallory M. [1 ]
Mehrotra, Pavni [1 ]
Nowak, Romana A. [1 ]
机构
[1] Univ Illinois, Dept Anim Sci, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED RECEPTOR; MATRIX METALLOPROTEINASE INDUCER; GROWTH-FACTOR RECEPTOR; ESTROGEN-RECEPTOR; BREAST-CANCER; PROLIFERATION; 17-BETA-ESTRADIOL; IDENTIFICATION; EXPRESSION; 4-HYDROXYTAMOXIFEN;
D O I
10.1210/jc.2012-2098
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Uterine remodeling is highly dependent on the glycosylated transmembrane protein extracellular matrix metalloproteinase (MMP) inducer (EMMPRIN). Previous studies indicate estradiol can increase EMMPRIN expression in uterine cells and promote subsequent induction of MMP production. Objective: The aim of this study was to investigate the role of G protein-coupled receptor 30 (GPR30) stimulation on EMMPRIN microvesicle release in the human uterine epithelial cell line hTERT-EEC (EECs). Design: We examined EMMPRIN release by human EECs in response to GPR30 stimulation by microvesicle isolation, Western blot, and immunocytochemistry. We employed a pharmacological approach using the GPR30-selective agonist G1 and the antagonist G15 to determine the receptor specificity of this response. Results: We demonstrated GPR30 expression in EECs and release of EMMPRIN in microvesicles in response to stimulation of GPR30. G1, estradiol, and cholera toxin stimulated EMMPRIN release in microvesicles as detected by Western blot and immunocytochemistry, indicating that stimulation of GPR30 can induce EMMPRIN microvesicle release. Conclusions: These data indicate that EMMPRIN release in microvesicles can be mediated by stimulation of GPR30 in human EECs, suggesting that inappropriate stimulation or expression of this receptor may be significant in uterine pathology. (J Clin Endocrinol Metab 97: 4613-4622, 2012)
引用
收藏
页码:4613 / 4622
页数:10
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