Upregulation of thrombomodulin expression by activation of farnesoid X receptor in vascular endothelial cells
Autor: | Yuan Li, Wei Gong, Bin Wang, Gang Huang, Yingru Zheng, Xie He, Zhizhen Xu, Li Zhang, Fengtian He |
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Rok vydání: | 2013 |
Předmět: |
Pharmacology
Regulation of gene expression Transcription Genetic Thrombomodulin Receptors Cytoplasmic and Nuclear Promoter Inflammation Biology Response Elements Up-Regulation Cell biology Nuclear receptor Downregulation and upregulation Human Umbilical Vein Endothelial Cells medicine Cancer research Humans Farnesoid X receptor medicine.symptom Promoter Regions Genetic Chromatin immunoprecipitation |
Zdroj: | European Journal of Pharmacology. 718:283-289 |
ISSN: | 0014-2999 |
DOI: | 10.1016/j.ejphar.2013.08.020 |
Popis: | Thrombomodulin (TM) serves as a vasoprotective molecule on the surface of vascular endothelial cells (VECs) to maintain the endothelial microenvironment by suppressing cellular proliferation, adhesion and inflammatory responses. Farnesoid X receptor (FXR), a nuclear receptor (NR) and originally considered as a bile acid-activated transcriptional factor, not only regulates metabolism homeostasis, but also influences cholesterol transport, vascular tension, and inflammation. Recent studies have shown that TM expression is upregulated by several NRs. However, it is unknown whether there is a link between FXR and TM. Our studies demonstrated that TM expression and activity were up-regulated by FXR activation in VECs. Reporter assays showed that FXR activation significantly enhanced the transcriptional activity of human TM gene promoter. Elecrophoretic mobility-shift and chromatin immunoprecipitation assays indicated that FXR induced TM expression by binding to a novel FXR-responsive element (FXRE), an inverted repeat DNA motif, IR8 (-503 AGGTCCtcccaaagTGCCCT-484) in the promoter region of TM gene. These results suggest that FXR may serve as a novel molecular target for manipulating TM expression and activity in VECs, which may be helpful for designing the therapeutic strategies to the treatment of associated diseases by targeting FXR/TM pathway. |
Databáze: | OpenAIRE |
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