Matches in SemOpenAlex for { <https://semopenalex.org/work/W2023130543> ?p ?o ?g. }
- W2023130543 endingPage "1759" @default.
- W2023130543 startingPage "1747" @default.
- W2023130543 abstract "Receptor activator of NF-κB ligand (RANKL) is a critical osteoclastogenic factor that is expressed on bone marrow stromal/preosteoblast cells. Most bone resorption stimuli induce osteoclast formation by modulating RANKL expression in these cells. However, little is known about the mechanisms regulating RANKL gene expression. We recently reported that heat shock factor-2 (HSF-2) is a downstream target for FGF-2 signaling to enhance RANKL gene transcription in marrow stromal/preosteoblast cells. In this study, we show that DACH1 (human homologue of Drosophila dachshund gene) negatively regulates RANKL gene expression and suppresses FGF-2-enhanced RANKL gene expression in these cells. DACH1 contains a conserved dachshund domain (DS) in the N-terminal region, which interacts with the nuclear co-repressor (NCoR) to repress gene expression. Co-expression of DACH1 with hRANKL promoter-luciferase reporter plasmid in normal human bone marrow-derived stromal cells significantly decreased (3.3-fold) FGF-2-stimulated hRANKL gene promoter activity. Deletion of DS domain abolished DACH1 inhibition of FGF-2-enhanced RANKL gene promoter activity. Western blot analysis confirmed that DACH1 suppressed FGF-2-stimulated RANKL expression in marrow stromal/preosteoblast cells. We show HSF-2 co-immune precipitated with DACH1 and that FGF-2 stimulation significantly increased (2.7-fold) HSF-2 binding to DACH1. Confocal microscopy analysis further demonstrated that FGF-2 promotes HSF-2 nuclear transport and co-localization with DACH1 in marrow stromal cells. Co-expression of NCoR with DACH1 significantly decreased (5.3-fold) and siRNA suppression of NCoR in DACH1 co-transfected cells increased (3.6-fold) RANKL promoter activity. Furthermore, DACH1 co-expression with NCoR significantly decreased (7.5-fold) RANKL mRNA expression in marrow stromal cells. Collectively, these studies indicate that NCoR participates in DACH1 repression of RANKL gene expression in marrow stromal/preosteoblast cells. Thus, DACH1 plays an important role in negative regulation of RANKL gene expression in marrow stromal/preosteoblast cells in the bone microenvironment. J. Cell. Biochem. 103: 1747–1759, 2008. © 2007 Wiley-Liss, Inc." @default.
- W2023130543 created "2016-06-24" @default.
- W2023130543 creator A5003237382 @default.
- W2023130543 creator A5005183715 @default.
- W2023130543 creator A5005801374 @default.
- W2023130543 creator A5016235708 @default.
- W2023130543 creator A5051947881 @default.
- W2023130543 creator A5079585951 @default.
- W2023130543 date "2008-01-01" @default.
- W2023130543 modified "2023-10-18" @default.
- W2023130543 title "DACH1 negatively regulates the human RANK ligand gene expression in stromal/preosteoblast cells" @default.
- W2023130543 cites W1534645474 @default.
- W2023130543 cites W1537244087 @default.
- W2023130543 cites W1904178031 @default.
- W2023130543 cites W1980267834 @default.
- W2023130543 cites W1985898496 @default.
- W2023130543 cites W1999032828 @default.
- W2023130543 cites W2002688584 @default.
- W2023130543 cites W2005040182 @default.
- W2023130543 cites W2018303721 @default.
- W2023130543 cites W2023991905 @default.
- W2023130543 cites W2029264336 @default.
- W2023130543 cites W2048299560 @default.
- W2023130543 cites W2048325346 @default.
- W2023130543 cites W2065784567 @default.
- W2023130543 cites W2069410160 @default.
- W2023130543 cites W2074110200 @default.
- W2023130543 cites W2074661703 @default.
- W2023130543 cites W2074760000 @default.
- W2023130543 cites W2080915541 @default.
- W2023130543 cites W2086805267 @default.
- W2023130543 cites W2088535641 @default.
- W2023130543 cites W2093349314 @default.
- W2023130543 cites W2093915139 @default.
- W2023130543 cites W2098273098 @default.
- W2023130543 cites W2101027724 @default.
- W2023130543 cites W2102948981 @default.
- W2023130543 cites W2106766464 @default.
- W2023130543 cites W2113047648 @default.
- W2023130543 cites W2114111754 @default.
- W2023130543 cites W2118371066 @default.
- W2023130543 cites W2119173715 @default.
- W2023130543 cites W2126530170 @default.
- W2023130543 cites W2127584433 @default.
- W2023130543 cites W2132675666 @default.
- W2023130543 cites W2136238864 @default.
- W2023130543 cites W2151199141 @default.
- W2023130543 cites W2159575937 @default.
- W2023130543 cites W2161392800 @default.
- W2023130543 cites W2167091901 @default.
- W2023130543 cites W2180121032 @default.
- W2023130543 doi "https://doi.org/10.1002/jcb.21561" @default.
- W2023130543 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2778848" @default.
- W2023130543 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17891780" @default.
- W2023130543 hasPublicationYear "2008" @default.
- W2023130543 type Work @default.
- W2023130543 sameAs 2023130543 @default.
- W2023130543 citedByCount "12" @default.
- W2023130543 countsByYear W20231305432012 @default.
- W2023130543 countsByYear W20231305432013 @default.
- W2023130543 countsByYear W20231305432014 @default.
- W2023130543 countsByYear W20231305432015 @default.
- W2023130543 countsByYear W20231305432016 @default.
- W2023130543 countsByYear W20231305432018 @default.
- W2023130543 countsByYear W20231305432021 @default.
- W2023130543 crossrefType "journal-article" @default.
- W2023130543 hasAuthorship W2023130543A5003237382 @default.
- W2023130543 hasAuthorship W2023130543A5005183715 @default.
- W2023130543 hasAuthorship W2023130543A5005801374 @default.
- W2023130543 hasAuthorship W2023130543A5016235708 @default.
- W2023130543 hasAuthorship W2023130543A5051947881 @default.
- W2023130543 hasAuthorship W2023130543A5079585951 @default.
- W2023130543 hasBestOaLocation W20231305432 @default.
- W2023130543 hasConcept C104317684 @default.
- W2023130543 hasConcept C125864771 @default.
- W2023130543 hasConcept C153911025 @default.
- W2023130543 hasConcept C16930146 @default.
- W2023130543 hasConcept C170493617 @default.
- W2023130543 hasConcept C185592680 @default.
- W2023130543 hasConcept C2776033226 @default.
- W2023130543 hasConcept C2779428903 @default.
- W2023130543 hasConcept C502942594 @default.
- W2023130543 hasConcept C54009773 @default.
- W2023130543 hasConcept C55493867 @default.
- W2023130543 hasConcept C86803240 @default.
- W2023130543 hasConcept C88045685 @default.
- W2023130543 hasConcept C95444343 @default.
- W2023130543 hasConceptScore W2023130543C104317684 @default.
- W2023130543 hasConceptScore W2023130543C125864771 @default.
- W2023130543 hasConceptScore W2023130543C153911025 @default.
- W2023130543 hasConceptScore W2023130543C16930146 @default.
- W2023130543 hasConceptScore W2023130543C170493617 @default.
- W2023130543 hasConceptScore W2023130543C185592680 @default.
- W2023130543 hasConceptScore W2023130543C2776033226 @default.
- W2023130543 hasConceptScore W2023130543C2779428903 @default.
- W2023130543 hasConceptScore W2023130543C502942594 @default.
- W2023130543 hasConceptScore W2023130543C54009773 @default.
- W2023130543 hasConceptScore W2023130543C55493867 @default.