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Cited 36 time in webofscience Cited 38 time in scopus
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Cell source-dependent in vivo immunosuppressive properties of mesenchymal stem cells derived from the bone marrow and synovial fluid of minipigs

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dc.contributor.authorLee, Won-Jae-
dc.contributor.authorHah, Young-Sool-
dc.contributor.authorOck, Sun-A.-
dc.contributor.authorLee, Jae-Hoon-
dc.contributor.authorJeon, Ryong-Hoon-
dc.contributor.authorPark, Ji-Sung-
dc.contributor.authorLee, Sang-Il-
dc.contributor.authorRho, Na-Young-
dc.contributor.authorRho, Gyu-Jin-
dc.contributor.authorLee, Sung-Lim-
dc.date.accessioned2022-12-26T21:36:41Z-
dc.date.available2022-12-26T21:36:41Z-
dc.date.issued2015-05-01-
dc.identifier.issn0014-4827-
dc.identifier.issn1090-2422-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/17248-
dc.description.abstractThe in vitro differentiation and immunosuppressive capacity of mesenchymal stem cells (MSCs) derived from synovial fluid (SF-MSCs) and bone marrow extract (BM-MSCs) in an isogenic background of minipigs were comparatively analyzed in a collagen-induced arthritis (CIA) mouse model of rheumatoid arthritis (RA). The proliferation capacity and expression of pluripotent transcription factors (Oct3/4 and Sox2) were significantly (P < 0.05) higher in SF-MSCs than in BM-MSCs. The differentiation capacity of SF-MSCs into adipocytes, osteocytes and neurocytes was significantly (P < 0.05) lower than that of BM-MSCs, and the differentiation capacity of SF-MSCs into chondrocytes was significantly (P < 0.05) higher than that of BM-MSCs. Systemic injection of BM- and SF-MSCs significantly (P < 0.05) ameliorated the clinical symptoms of CIA mice, with SF-MSCs having significantly (P < 0.05) higher clinical and histopathological recovery scores than BM-MSCs. Furthermore, the immunosuppressive properties of SF-MSCs in CIA mice were associated with increased levels of the anti-inflammatory cytokine interleukin (IL)-10, and decreased levels of the pro-inflammatory cytokine IL-1 beta and osteoclast-related sRANKL. In conclusion, SF-MSCs exhibited eminent pluripotency and differentiation capacity into chondrocytes, addition to substantial in vivo immunosuppressive capacity by elevating IL-10 and reducing IL-1 beta levels in CIA mice. (C) 2015 The Authors. Published by Elsevier Inc.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER INC-
dc.titleCell source-dependent in vivo immunosuppressive properties of mesenchymal stem cells derived from the bone marrow and synovial fluid of minipigs-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.yexcr.2015.03.015-
dc.identifier.scopusid2-s2.0-84927911350-
dc.identifier.wosid000353666100015-
dc.identifier.bibliographicCitationEXPERIMENTAL CELL RESEARCH, v.333, no.2, pp 273 - 288-
dc.citation.titleEXPERIMENTAL CELL RESEARCH-
dc.citation.volume333-
dc.citation.number2-
dc.citation.startPage273-
dc.citation.endPage288-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusCOLLAGEN-INDUCED ARTHRITIS-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusSTROMAL CELLS-
dc.subject.keywordPlusGENE-TRANSFER-
dc.subject.keywordPlusVIRAL IL-10-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusRESPONSES-
dc.subject.keywordPlusADIPOSE-
dc.subject.keywordPlusOSTEOCLASTOGENESIS-
dc.subject.keywordPlusINTERLEUKIN-10-
dc.subject.keywordAuthorMesenchymal stem cell-
dc.subject.keywordAuthorSynovial fluid-
dc.subject.keywordAuthorImmunomodulation-
dc.subject.keywordAuthorDifferentiation-
dc.subject.keywordAuthorRheumatoid arthritis-
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