(HEPATOLOGY 2010.) Estrogens promote female reproductive

organ development and function, but estrogen receptors (ERs) are also found, at lower levels, in the skin,1 intestine,2 brain,3 and liver4 where they exert significant influence over diverse aspects of cellular physiology. For example, in the skin, the transition from cyclical estrogen fluctuations during reproductive life to an estrogen deficiency after menopause is associated with dryness, atrophy, fine wrinkling, and poor wound healing.5 JNK inhibitor mouse Estrogens also intimately regulate interleukin-6 (IL-6) expression in various cell types.6 IL-6 is also critical to epithelial barrier function and wound healing in the skin7 and gastrointestinal8 and biliary tracts.9 For example, estrogens inhibit macrophage IL-6 production, which in turn, maintains serum IL-6 levels at relatively low levels during reproductive Gemcitabine purchase years.10 Menopausal loss of estrogens elevates serum IL-6 levels,

which in turn, stimulates osteoclastic bone resorption.6, 11 IL-6−/− mice, however, are resistant to the osteopenic complications of estrogen deficiency.12 In contrast, estrogen stimulates IL-6 production in human ovarian epithelial cells and ovarian cancer cells.13 Promoter complexity controlling IL-6 gene expression14 and complexity of estrogen signaling15, 16 contribute to the tissue-specific regulation of IL-6 expression by estrogens. Estrogens influence biliary tract pathophysiology.17

Females are significantly MCE公司 more susceptible than males to several chronic liver diseases that involve either the biliary tree and/or are influenced by IL-6 expression. Included in these chronic diseases are: (1) primary biliary cirrhosis (PBC),18 a disease associated with variations of IL-6 production19, 20; (2) debilitating/symptomatic adult polycystic liver disease (PCL) requiring liver transplantation,17 in which cyst fluid contains high levels of IL-621; and (3) autoimmune hepatitis, which requires IL-6 production to sustain T helper 17 (TH17)-type T lymphocytes that are critical to disease development.22 These observations raise the hypothesis that estrogens might influence biliary epithelial cell (BEC) IL-6 expression and thereby affect barrier epithelial function, wound repair, and peribiliary or portal tract immune responses. Using primary cultures of non-neoplastic mouse BECs (mBECs) and two human cholangiocarcinoma cell lines, we show that estrogens can stimulate BEC IL-6 production, but only in female or ERα-expressing neoplastic BECs. Estrogen-induced BEC IL-6 production, in turn, is related to ERα expression, which is higher in female than male BECs. Consequently, female BECs are more dependent on the trophic influences of estrogen for continued survival in vitro, and estrogen-induced stimulation of BEC growth can be inhibited by anti–IL-6 antibodies.