The mitogenic potential of heparin-binding epidermal growth factor in the human endometrium is mediated by the epidermal growth factor receptor and is modulated by tumor necrosis factor-α

被引:34
作者
Chobotova, K
Muchmore, ME
Carver, J
Yoo, HJ
Manek, S
Gullick, WJ
Barlow, DH
Mardon, HJ
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Obstet & Gynecol, Womens Ctr, Oxford OX3 9DU, England
[2] Univ Kent, Res Sch Biosci, Canterbury CT2 7NJ, Kent, England
基金
英国惠康基金;
关键词
D O I
10.1210/jc.2002-020069
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heparin-binding epidermal growth factor (HB-EGF), a member of the epidermal growth factor (EGF) family, is implicated in a variety of biological processes, including reproduction. Previous studies describe increased levels of HB-EGF in the human endometrium during the midsecretory stage of the menstrual cycle, suggesting a function for HB-EGF in implantation of the human blastocyst. Here we have investigated the expression and function of the soluble and transmembrane forms of HB-EGF in the human endometrium. We show that the expression of the transmembrane form of HB-EGF in the human endometrium is modulated according to the stage of the menstrual cycle. We present data demonstrating that both the soluble and transmembrane forms of HB-EGF induce DNA synthesis in human endometrial stromal cells. Furthermore, TNFalpha has a cooperative effect on HB-EGF, EGF, TGFalpha, and betacellulin-induced DNA synthesis in stromal cells, suggesting roles for the EGF family and TNFalpha in regeneration and maturation of human endometrium. Induction of DNA synthesis by HB-EGF and its modulation by TNFa in endometrial stromal cells are mediated by the EGF receptor and not the HB-EGF receptor Erb134. Our data suggest key functions for HB-EGF, TNFalpha, and the EGF receptor in endometrial maturation, via autocrine/paracrine and juxtacrine pathways, in preparation for embryo implantation.
引用
收藏
页码:5769 / 5777
页数:9
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