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Cited 4 time in webofscience Cited 5 time in scopus
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Poly-γ-glutamic acid suppresses osteoclastogenesis in human osteoclast precursors and prevents joint damage in a collagen-induced murine arthritis model

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dc.contributor.authorLee, Bitnara-
dc.contributor.authorJo, Sungsin-
dc.contributor.authorKim, Sung-Min-
dc.contributor.authorCho, Mi-La-
dc.contributor.authorPark, Sung-Hwan-
dc.contributor.authorYoun, Jeehee-
dc.contributor.authorJi, Jong Dae-
dc.contributor.authorKim, Tae-Hwan-
dc.date.accessioned2021-07-30T05:00:54Z-
dc.date.available2021-07-30T05:00:54Z-
dc.date.created2021-05-12-
dc.date.issued2018-11-
dc.identifier.issn0165-2478-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/2664-
dc.description.abstractPoly–γ-glutamic acid (γ-PGA), a natural polymer derived from Bacillus subtilis, shows anti-inflammatory activity. However, the effects of γ-PGA on osteoclasts, which are important cells for joint destruction in inflammatory diseases such as rheumatoid arthritis (RA), have not yet been reported. In this study, we show that γ-PGA markedly inhibits osteoclast differentiation in normal PBMC-derived osteoclast precursors and in synovial fluid macrophages of patients with RA. γ-PGA also reduces RANK expression by down-regulating M-CSF receptors. Additionally, oral administration of γ-PGA attenuated bone destruction in a collagen-induced arthritis (CIA) model, demonstrating decreases in inflammation, cartilage damage, and osteoclast formation in histological analyses. Taken together, these data suggest that γ-PGA could be a good candidate for therapeutic prevention of joint destruction in RA.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.titlePoly-γ-glutamic acid suppresses osteoclastogenesis in human osteoclast precursors and prevents joint damage in a collagen-induced murine arthritis model-
dc.title.alternativePoly-gamma-glutamic acid suppresses osteoclastogenesis in human osteoclast precursors and prevents joint damage in a collagen-induced murine arthritis model-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoun, Jeehee-
dc.contributor.affiliatedAuthorKim, Tae-Hwan-
dc.identifier.doi10.1016/j.imlet.2018.09.004-
dc.identifier.scopusid2-s2.0-85054067329-
dc.identifier.wosid000455063700014-
dc.identifier.bibliographicCitationIMMUNOLOGY LETTERS, v.203, pp.80 - 86-
dc.relation.isPartOfIMMUNOLOGY LETTERS-
dc.citation.titleIMMUNOLOGY LETTERS-
dc.citation.volume203-
dc.citation.startPage80-
dc.citation.endPage86-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusRECEPTOR ACTIVATOR-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusEFFICACY-
dc.subject.keywordPlusTREM-2-
dc.subject.keywordPlusRANKL-
dc.subject.keywordPlusMICE-
dc.subject.keywordAuthorPoly-gamma-glutamic acid (gamma-PGA)-
dc.subject.keywordAuthorOsteoclast-
dc.subject.keywordAuthorRheumatoid arthritis-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0165247818302104?via%3Dihub-
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서울 의과대학 > 서울 내과학교실 > 1. Journal Articles
서울 의과대학 > 서울 해부·세포생물학교실 > 1. Journal Articles

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