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The Effect of Calcipotriol on the Expression of Human beta Defensin-2 and LL-37 in Cultured Human Keratinocytes

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dc.contributor.authorKim, Beom Joon-
dc.contributor.authorRho, Yong Kwan-
dc.contributor.authorLee, Hye In-
dc.contributor.authorJeong, Mi Sook-
dc.contributor.authorLi, Kapsok-
dc.contributor.authorSeo, Seong Jun-
dc.contributor.authorKim, Myeung Nam-
dc.contributor.authorHong, Chang Kwun-
dc.date.available2019-05-30T04:34:02Z-
dc.date.issued2009-
dc.identifier.issn1740-2522-
dc.identifier.issn1740-2530-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23489-
dc.description.abstractBackground. Vitamin D has been reported to regulate innate immunity by controlling the expression of antimicrobial peptides (AMPs). Objective. We investigated the effect of calcipotriol on the expression of AMPs in human cultured keratinocytes. Methods. Keratinocytes were treated with lipopolysaccharide (LPS), TNF-alpha, Calcipotriol and irradiated with UVB, cultured, and harvested. To assess the expression of human beta defensin-2 and LL-37 in the control group, not exposed to any stimulants, the experimental group was treated with LPS, TNF-alpha, or UVB, and another group was treated again with calcipotriol; reverse transcriptase-polymerase chain reaction, Western blotting, and immunohistochemical staining were performed. Results. In the experimental group treated with LPS, UVB irradiation, and TNF-alpha, the expression of beta-defensin and LL-37 was increased more than in the control group and then decreased in the experimental group treated with calcipotriol. Conclusions. Calcipotriol suppressed HBD-2 and LL-37, which were stimulated by UVB, LPS, and TNF-alpha. Copyright (C) 2009 Beom Joon Kim et al.-
dc.language영어-
dc.language.isoENG-
dc.publisherHINDAWI LTD-
dc.titleThe Effect of Calcipotriol on the Expression of Human beta Defensin-2 and LL-37 in Cultured Human Keratinocytes-
dc.typeArticle-
dc.identifier.doi10.1155/2009/645898-
dc.identifier.bibliographicCitationCLINICAL & DEVELOPMENTAL IMMUNOLOGY, v.2009-
dc.description.isOpenAccessN-
dc.identifier.wosid000276066300001-
dc.identifier.scopusid2-s2.0-77749314934-
dc.citation.titleCLINICAL & DEVELOPMENTAL IMMUNOLOGY-
dc.citation.volume2009-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusANTIMICROBIAL PEPTIDES-
dc.subject.keywordPlusHUMAN SKIN-
dc.subject.keywordPlus1,25-DIHYDROXYVITAMIN D-3-
dc.subject.keywordPlusHUMAN BETA-DEFENSIN-2-
dc.subject.keywordPlusCATHELICIDIN LL-37-
dc.subject.keywordPlusATOPIC-DERMATITIS-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusRETINOIC ACID-
dc.subject.keywordPlusIMMUNITY-
dc.subject.keywordPlusINDUCTION-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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