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Co-culture of human bone marrow mesenchymal stem cells and macrophages attenuates lipopolysaccharide-induced inflammation in human corneal epithelial cells

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dc.contributor.authorJeong, Won-Yong-
dc.contributor.authorKim, Ji-Hye-
dc.contributor.authorKim, Chan-Wha-
dc.date.accessioned2021-09-02T21:23:13Z-
dc.date.available2021-09-02T21:23:13Z-
dc.date.created2021-06-16-
dc.date.issued2018-
dc.identifier.issn0916-8451-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/81015-
dc.description.abstractDry eye syndrome (DES) is considered as an ocular surface inflammatory disease. Previous studies have shown inflammation plays an important role in the progression and onset of DES. Co-culture of human bone marrow mesenchymal stem cells (HBMSCs) and macrophages showed immunomodulatory effects via regulation of cytokine regulation. Thus, the aim of this study was to investigate the effect of the interaction of these cells on in vitro DES model. The conditioned media (CM) from macrophages, HBMSCs, and HBMSCs+macrophages were treated to human corneal epithelial cells, which showed significant reduction in IL-1 and IL-1 expression levels in HBMSCs+macrophages group. Moreover, the IL-1 Receptor Antagonist (IL-1RA) was highly expressed in the CM from the HBMSCs+macrophages group. Wounded eyes of mice were treated with IL-1RA at 0-100ng/mL for 16h, the wound size was reduced. The results of this study might lead to the identification of new therapeutic targets for DES.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectDRY-EYE DISEASE-
dc.subjectIL-1 RECEPTOR ANTAGONIST-
dc.subjectSTROMAL CELLS-
dc.subjectHUMAN MONOCYTES-
dc.subjectOCULAR SURFACE-
dc.subjectINTERLEUKIN-1-
dc.subjectALBUMIN-
dc.subjectINJURY-
dc.subjectSUPPRESSION-
dc.subjectTHERAPY-
dc.titleCo-culture of human bone marrow mesenchymal stem cells and macrophages attenuates lipopolysaccharide-induced inflammation in human corneal epithelial cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chan-Wha-
dc.identifier.doi10.1080/09168451.2018.1438167-
dc.identifier.scopusid2-s2.0-85046693359-
dc.identifier.wosid000430803400008-
dc.identifier.bibliographicCitationBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, v.82, no.5, pp.800 - 809-
dc.relation.isPartOfBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY-
dc.citation.titleBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY-
dc.citation.volume82-
dc.citation.number5-
dc.citation.startPage800-
dc.citation.endPage809-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusDRY-EYE DISEASE-
dc.subject.keywordPlusIL-1 RECEPTOR ANTAGONIST-
dc.subject.keywordPlusSTROMAL CELLS-
dc.subject.keywordPlusHUMAN MONOCYTES-
dc.subject.keywordPlusOCULAR SURFACE-
dc.subject.keywordPlusINTERLEUKIN-1-
dc.subject.keywordPlusALBUMIN-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusSUPPRESSION-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordAuthorMesenchymal stem cells-
dc.subject.keywordAuthordry eye syndrome-
dc.subject.keywordAuthorhuman corneal epithelial cells-
dc.subject.keywordAuthorIL-1 Receptor Antagonist-
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