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Cited 6 time in webofscience Cited 6 time in scopus
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2-(Trimethylammonium) Ethyl (R)-3-Methoxy-3-oxo-2-Stearamidopropyl Phosphate Suppresses Osteoclast Maturation and Bone Resorption by Targeting Macrophage-Colony Stimulating Factor Signaling

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dc.contributor.authorPark, So Jeong-
dc.contributor.authorPark, Doo Ri-
dc.contributor.authorBhattarai, Deepak-
dc.contributor.authorLee, Kyeong-
dc.contributor.authorKim, Jaesang-
dc.contributor.authorBae, Yun Soo-
dc.contributor.authorLee, Soo Young-
dc.date.accessioned2024-08-08T01:31:15Z-
dc.date.available2024-08-08T01:31:15Z-
dc.date.issued2014-08-31-
dc.identifier.issn1016-8478-
dc.identifier.issn0219-1032-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/15254-
dc.description.abstract2-(Trimethylammonium) ethyl (R)/3-methoxy-3-oxo-2-steara-midopropyl phosphate [(R)-TEMOSPho], a derivative of an organic chemical identified from a natural product library, promotes highly efficient megakaryopoiesis. Here, we show that (R)-TEMOSPho blocks osteoclast maturation from progenitor cells of hematopoietic origin, as well as blocking the resorptive function of mature osteoclasts. The inhibitory effect of (R)-TEMOSPho on osteoclasts was due to a disruption of the actin cytoskeleton, resulting from impaired downstream signaling of c-Fms, a receptor for macrophage-colony stimulating factor linked to c-Cbl, phosphoinositol-3-kinase (PI3K), Vav3, and Rac1. In addition, (R)-TEMOSPho blocked inflammation-induced bone destruction by reducing the numbers of osteoclasts produced in mice. Thus, (R)-TEMOSPho may represent a promising new class of antiresorptive drugs for the treatment of bone loss associated with increased osteoclast maturation and activity.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC MOLECULAR & CELLULAR BIOLOGY-
dc.title2-(Trimethylammonium) Ethyl (R)-3-Methoxy-3-oxo-2-Stearamidopropyl Phosphate Suppresses Osteoclast Maturation and Bone Resorption by Targeting Macrophage-Colony Stimulating Factor Signaling-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.14348/molcells.2014.0190-
dc.identifier.scopusid2-s2.0-84950159270-
dc.identifier.wosid000342561500009-
dc.identifier.bibliographicCitationMOLECULES AND CELLS, v.37, no.8, pp 628 - 635-
dc.citation.titleMOLECULES AND CELLS-
dc.citation.volume37-
dc.citation.number8-
dc.citation.startPage628-
dc.citation.endPage635-
dc.type.docTypeArticle-
dc.identifier.kciidART001907146-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusRHO-GTPASES-
dc.subject.keywordPlusC-FMS-
dc.subject.keywordPlusCELL BIOLOGY-
dc.subject.keywordPlusFACTOR-I-
dc.subject.keywordPlusM-CSF-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusCYTOSKELETON-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusDEFECTS-
dc.subject.keywordAuthorantiresorptive drugs-
dc.subject.keywordAuthorbone destruction-
dc.subject.keywordAuthorosteoclast-
dc.subject.keywordAuthorosteoclast maturation-
dc.subject.keywordAuthor(R)-TEMOSPho-
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