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Alleviation of imiquimod-induced psoriasis-like symptoms in Rorα-deficient mouse skin

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dc.contributor.authorPark, Koog Chan-
dc.contributor.authorKim, Jiwon-
dc.contributor.authorLee, Aram-
dc.contributor.authorLim, Jong-Seok-
dc.contributor.authorKim, Keun Il-
dc.date.accessioned2023-12-19T04:01:32Z-
dc.date.available2023-12-19T04:01:32Z-
dc.date.issued2023-05-
dc.identifier.issn1976-6696-
dc.identifier.issn1976-670X-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/159483-
dc.description.abstractRetinoic acid receptor-related orphan receptor α (RORα) plays a vital role in various physiological processes, including metabolism, cancer, circadian rhythm, cerebellar development, and inflammation. Although RORα is expressed in the skin, its role in skin physiology remains poorly elucidated. Herein, Rorα was expressed in the basal and suprabasal layers of the epidermis; however, keratinocyte-specific Rorα deletion did not impact normal epidermal formation. Under pathophysiological conditions, Rorα-deficient mice exhibited alleviated psoriasis-like symptoms, including relatively intact epidermal stratification, reduced keratinocyte hyperproliferation, and low-level expression of inflammatory cytokines in keratinocytes. Unexpectedly, the splenic population of Th17 cells was significantly lower in keratinocytespecific RORα deficient mice than in the control. Additionally, Rorα-deficiency reduced imiquimod-induced activation of nuclear factor-κB and STAT3 in keratinocytes. Therefore, we expect that RORα inhibitors act on immune cells and keratinocytes to suppress the onset and progression of psoriasis.as an adjuvant for cancer immunotherapy. [BMB Reports 2023; 56(5): 296-301].-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisher생화학분자생물학회-
dc.titleAlleviation of imiquimod-induced psoriasis-like symptoms in Rorα-deficient mouse skin-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.5483/BMBRep.2022-0169-
dc.identifier.scopusid2-s2.0-85160206504-
dc.identifier.wosid001079673200004-
dc.identifier.bibliographicCitationBMB reports, v.56, no.5, pp 296 - 301-
dc.citation.titleBMB reports-
dc.citation.volume56-
dc.citation.number5-
dc.citation.startPage296-
dc.citation.endPage301-
dc.type.docTypeArticle-
dc.identifier.kciidART002961630-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusCHOLESTEROL SULFATE-
dc.subject.keywordPlusKERATINOCYTES-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusLIGAND-
dc.subject.keywordPlusSTAT3-
dc.subject.keywordAuthorImiquimod-
dc.subject.keywordAuthorKeratinocytes-
dc.subject.keywordAuthorPsoriasis-
dc.subject.keywordAuthorRORα-
dc.subject.keywordAuthorSTAT3-
dc.identifier.urlhttps://kiss.kstudy.com/Detail/Ar?key=4019825-
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