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The Photoprotective Effect of S-Methylmethionine Sulfonium in Skin.

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dc.contributor.authorKim, Won-Serk-
dc.contributor.authorSeo, Hyun Min-
dc.contributor.authorKim, Wang-Kyun-
dc.contributor.authorChoi, Joon-Seok-
dc.contributor.authorKim, Ikyon-
dc.contributor.authorSung, Jong-Hyuk-
dc.date.accessioned2022-07-16T01:09:02Z-
dc.date.available2022-07-16T01:09:02Z-
dc.date.created2021-05-13-
dc.date.issued2015-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/158235-
dc.description.abstractS-Methylmethionine sulfonium (SMMS) was reported to have wound-healing effects; we therefore have investigated the photoprotective effect of SMMS in the present study. SMMS increased the viability of keratinocyte progenitor cells (KPCs) and human dermal fibroblasts (hDFs) following ultraviolet B (UVB) irradiation, and reduced the UVB-induced apoptosis in these cells. SMMS increased the phosphorylation of extracellular signal-regulated kinases (ERK), and the inhibitor of the mitogen-activated protein kinase pathway significantly decreased the SMMS-induced viability of KPCs and hDFs. In addition, SMMS attenuated the UVB-induced reactive oxygen species (ROS) generation in KPCs and hDFs. SMMS induced the collagen synthesis and reduced the matrix metalloproteinase-1 expression in UVB-irradiated hDFs. In animal studies, application of 5% and 10% SMMS before and after UVB-irradiation significantly decreased the UVB-induced erythema index and depletion of Langerhans cells. In summary, SMMS protects KPCs and hDFs from UVB irradiation, and reduces UVB-induced skin erythema and immune suppression. Therefore, SMMS can be used as a cosmetic raw material, and protect skin from UVB.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI AG-
dc.titleThe Photoprotective Effect of S-Methylmethionine Sulfonium in Skin.-
dc.typeArticle-
dc.contributor.affiliatedAuthorSeo, Hyun Min-
dc.identifier.doi10.3390/ijms160817088-
dc.identifier.scopusid2-s2.0-84938153204-
dc.identifier.wosid000366826100022-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.16, no.8, pp.17088 - 17100-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume16-
dc.citation.number8-
dc.citation.startPage17088-
dc.citation.endPage17100-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusDERMAL FIBROBLAST-
dc.subject.keywordPlusINDUCED ERYTHEMA-
dc.subject.keywordPlusUVB-
dc.subject.keywordPlusP53-
dc.subject.keywordPlusRADIATION-
dc.subject.keywordPlusCHLORIDE-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSENESCENCE-
dc.subject.keywordAuthorDermal fibroblasts-
dc.subject.keywordAuthorErythema-
dc.subject.keywordAuthorKeratinocyte progenitor cells-
dc.subject.keywordAuthorS-methylmethionine sulfonium-
dc.subject.keywordAuthorUVB protection-
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