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Regulation of TREM-1 expression by 1,25-dihydroxyvitamin D-3 in human monocytes/macrophages

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dc.contributor.authorKim, Tae-Hwan-
dc.contributor.authorLee, Bitnara-
dc.contributor.authorKwon, Eunji-
dc.contributor.authorChoi, Sung Jae-
dc.contributor.authorLee, Young Ho-
dc.contributor.authorSong, Gwan Gyu-
dc.contributor.authorSohn, Jeongwon-
dc.contributor.authorJi, Jong Dae-
dc.date.accessioned2021-09-06T00:11:38Z-
dc.date.available2021-09-06T00:11:38Z-
dc.date.created2021-06-14-
dc.date.issued2013-07-
dc.identifier.issn0165-2478-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102825-
dc.description.abstractTriggering receptor expressed on myeloid cells-1 (TREM-1) is a recently identified cell surface receptor that is expressed mainly on monocytes and neutrophils, and acts as an amplifier of immune responses. In this study, 1,25(OH)(2)D-3 strongly upregulated the expression of TEEM-1 in human monocytes and macrophages. 1,25(OH)(2)D-3 stimulated TREM-1 mRNA expression by augmenting transcription, and not by inhibiting mRNA degradation. The upregulated expression of TREM-1 by 1,25(OH)(2)D-3 was dependent on the NF-kappa B signaling pathway and required new protein synthesis in differentiated U937 macrophages. Our results show that 1,25(OH)(2)D-3 can affect the innate and inflammatory responses by upregulating TEEM-1 expression, and suggest that 1,25(OH)(2)D-3 may function as an enhancer of the innate immune response by upregulating TREM-1 expression, in addition to inducing the antimicrobial peptide cathelicidin. (C) 2013 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectMYELOID CELLS-1-
dc.subjectVITAMIN-D-
dc.subjectEPITHELIAL-CELLS-
dc.subjectCUTTING EDGE-
dc.subjectRECEPTOR-
dc.subjectMACROPHAGES-
dc.subjectENDOTOXEMIA-
dc.subjectINDUCTION-
dc.subjectMONOCYTES-
dc.titleRegulation of TREM-1 expression by 1,25-dihydroxyvitamin D-3 in human monocytes/macrophages-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Sung Jae-
dc.contributor.affiliatedAuthorLee, Young Ho-
dc.contributor.affiliatedAuthorSong, Gwan Gyu-
dc.contributor.affiliatedAuthorSohn, Jeongwon-
dc.contributor.affiliatedAuthorJi, Jong Dae-
dc.identifier.doi10.1016/j.imlet.2013.08.012-
dc.identifier.scopusid2-s2.0-84884336462-
dc.identifier.wosid000326559400013-
dc.identifier.bibliographicCitationIMMUNOLOGY LETTERS, v.154, no.1-2, pp.80 - 85-
dc.relation.isPartOfIMMUNOLOGY LETTERS-
dc.citation.titleIMMUNOLOGY LETTERS-
dc.citation.volume154-
dc.citation.number1-2-
dc.citation.startPage80-
dc.citation.endPage85-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusMYELOID CELLS-1-
dc.subject.keywordPlusVITAMIN-D-
dc.subject.keywordPlusEPITHELIAL-CELLS-
dc.subject.keywordPlusCUTTING EDGE-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusMACROPHAGES-
dc.subject.keywordPlusENDOTOXEMIA-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusMONOCYTES-
dc.subject.keywordAuthorTREM-1-
dc.subject.keywordAuthor1,25-Dihydroxyviamin D-3-
dc.subject.keywordAuthorMonocytes-
dc.subject.keywordAuthorMacrophages-
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