Regulation of the human oxytocin receptor by nuclear factor-kappa B and CCAAT/enhancer-binding protein-beta
Terzidou, Vasso, Lee, Yooni, Lindstrom, Tamsin, Johnson, Mark, Thornton, Steven and Bennett, Phillip R.. (2013) Regulation of the human oxytocin receptor by nuclear factor-kappa B and CCAAT/enhancer-binding protein-beta. Journal of Clinical Endocrinology & Metabolism , Volume 91 (Number 6). pp. 2317-2326. ISSN 0021-972xFull text not available from this repository.
Official URL: http://dx.doi.org/10.1210/jc.2005-2649
Context: Increased myometrial sensitivity to oxytocin at term is mediated through increased oxytocin receptor (OTR) expression. OTR promoter contains putative transcription factor-binding sites for activating protein-1 (AP-1), CCAAT/enhancer-binding protein (C/EBP), and nuclear factor-kappa B (NF-kappa B), which may be activated by IL-1 beta, whose concentrations increase with labor.
Objective: The objective of this study was to examine the effect of IL-1 beta on OTR expression and the roles of AP-1, C/EBP, and NF-kappa B in OTR promoter function.
Results: IL-1 beta induces an increase in OTR mRNA concentrations and OTR ligand binding in myometrial cells, which is maximal at 4 h and decreased after 20 h. IL-1 beta activates the transcription factors AP-1 C/EBP beta, and NF-kappa B. Using computer-based analysis and EMSA studies, we have identified three AP-1, nine C/EBP, and three NF-kappa B DNA-binding sites in the OTR promoter. In transient transfection studies, OTR promoter activity was increased by C/EBP beta and NF-kappa B, but not by AP-1. C/EBP beta and NF-kappa B together had a synergistic action in the induction of OTR promoter activity. Site-directed mutagenesis of each individual C/EBP and NF-kappa B site had no effect on the ability of C/EBP beta, NF-kappa B, or their combination to activate OTR promoter. However, mutation of both NF-kappa B sites inhibited promoter activation by NF-kappa B alone, but not that by the combination of C/EBP beta and NF-kappa B. Deletion studies showed that a region between -851 and -656 of the OTR confers responsiveness to the combination of C/EBP beta and NF-kappa B.
Conclusion: IL-1 beta has a biphasic effect on OTR expression in myometrial cells, and C/EBP and NF-kappa B play synergistic roles in OTR promoter activation.
|Item Type:||Journal Article|
|Subjects:||R Medicine > RC Internal medicine|
|Divisions:||Faculty of Medicine > Warwick Medical School > Health Sciences
Faculty of Medicine > Warwick Medical School > Translational & Systems Medicine > Reproductive Health
Faculty of Medicine > Warwick Medical School
|Journal or Publication Title:||Journal of Clinical Endocrinology & Metabolism|
|Official Date:||20 July 2013|
|Number of Pages:||10|
|Page Range:||pp. 2317-2326|
|Access rights to Published version:||Restricted or Subscription Access|
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