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Expression and modulation of LL-37 in normal human keratinocytes, HaCaT cells, and inflammatory skin diseases

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dc.contributor.authorKim, JE-
dc.contributor.authorKim, BJ-
dc.contributor.authorJeong, MS-
dc.contributor.authorSeo, SJ-
dc.contributor.authorKim, MN-
dc.contributor.authorHong, CK-
dc.contributor.authorRo, BI-
dc.date.available2019-05-30T07:37:19Z-
dc.date.issued2005-08-
dc.identifier.issn1011-8934-
dc.identifier.issn1598-6357-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24553-
dc.description.abstractDefensins and cathelicidins (LL-37) are major antimicrobial peptides (AMPs) of the innate immune system of the human skin. In normal non-inflamed skin these peptides are negligible, but their expression can be markedly increased in inflammatory skin disease such as psoriasis. We designed this study to identify the expressions of LL-37 in normal human keratinocyte (NHK) and HaCaT cells after exposure to stimulants and to investigate difference of LL-37 expression accompanied with cell differentiation status, and come to understand difference of susceptibility to infection in atopic dermatitis and psoriasis. Expressions of LL-37 in NHKs and HaCaT cells were evaluated by using RT-PCR, Western blotting, and immunohistochemical (IHC) staining at 6, 12, and 24 hr post stimulation after exposure to Ultraviolet B irradiation and lipopolysaccharide. And expression of LL-37 in skin biopsy specimens from patients with atopic dermatitis and psoriasis was determined by immunohistochemical analysis. In time-sequential analyses of LL-37 expression revealed that LL-37 was expressed in NHKs, but not in HaCaT cells. IHC analysis confirmed the presence of abundant LL-37 in the epidermis of psoriasis. Therefore we deduced that expression of LL-37 is affected by UV irradiation, bacterial infection, and status of cell differentiation.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN ACAD MEDICAL SCIENCES-
dc.titleExpression and modulation of LL-37 in normal human keratinocytes, HaCaT cells, and inflammatory skin diseases-
dc.typeArticle-
dc.identifier.doi10.3346/jkms.2005.20.4.649-
dc.identifier.bibliographicCitationJOURNAL OF KOREAN MEDICAL SCIENCE, v.20, no.4, pp 649 - 654-
dc.identifier.kciidART000967559-
dc.description.isOpenAccessN-
dc.identifier.wosid000231633500021-
dc.identifier.scopusid2-s2.0-24644496354-
dc.citation.endPage654-
dc.citation.number4-
dc.citation.startPage649-
dc.citation.titleJOURNAL OF KOREAN MEDICAL SCIENCE-
dc.citation.volume20-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorCAP18 lipopolysaccharide-binding protein-
dc.subject.keywordAuthorLL-37-
dc.subject.keywordAuthorkeratinocytes-
dc.subject.keywordAuthorHaCaT cell-
dc.subject.keywordAuthorpsoriasis-
dc.subject.keywordAuthordermatitis-
dc.subject.keywordAuthoratopic-
dc.subject.keywordPlusCATHELICIDIN ANTIMICROBIAL PEPTIDES-
dc.subject.keywordPlusINVASIVE BACTERIAL-INFECTION-
dc.subject.keywordPlusATOPIC-DERMATITIS-
dc.subject.keywordPlusSALIVARY-GLANDS-
dc.subject.keywordPlusBETA-DEFENSINS-
dc.subject.keywordPlusINNATE DEFENSE-
dc.subject.keywordPlusIMMUNITY-
dc.subject.keywordPlusPROTEIN-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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