Terrein: a new melanogenesis inhibitor and its mechanism

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dc.contributor.authorS H Park-
dc.contributor.authorD S Kim-
dc.contributor.authorWon Gon Kim-
dc.contributor.authorIn Ja Ryoo-
dc.contributor.authorD H Lee-
dc.contributor.authorC H Huh-
dc.contributor.authorS W Youn-
dc.contributor.authorIck Dong Yoo-
dc.contributor.authorK C Park-
dc.date.accessioned2017-04-19T09:01:49Z-
dc.date.available2017-04-19T09:01:49Z-
dc.date.issued2004-
dc.identifier.issn1420-682X-
dc.identifier.uri10.1007/s00018-004-4341-3ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6714-
dc.description.abstractTerrein is a bioactive fungal metabolite whose effects are almost unknown. In this study, we found for the first time that terrein has a strong hypopigmentary effect in a spontaneously immortalized mouse melanocyte cell line, Mel-Ab. Treatment of Mel-Ab cells with terrein (10-100 μM) for 4 days significantly reduced melanin levels in a dose-dependent manner. In addition, terrein at the same concentration also reduced tyrosinase activity. We then investigated whether terrein influences the extracellular signal-regulated protein kinase (ERK) pathway and the expression of microphthalmia-associated transcription factor (MITF), which is required for tyrosinase expression. Terrein was found to induce sustained ERK activation and MITF down-regulation, and luciferase assays showed that terrein inhibits MITF promoter activity in a dose-dependent manner. To elucidate the correlation between ERK pathway activation and a decreased MITF transcriptional level, PD98059, a specific inhibitor of the ERK pathway, was applied before terrein treatment and found to abrogate the terrein-induced MITF attenuation. Terrein also reduced the tyrosinase protein level for at least 72 h. These results suggest that terrein reduces melanin synthesis by reducing tyrosinase production via ERK activation, and that this is followed by MITF down-regulation.-
dc.publisherSpringer-
dc.titleTerrein: a new melanogenesis inhibitor and its mechanism-
dc.title.alternativeTerrein: a new melanogenesis inhibitor and its mechanism-
dc.typeArticle-
dc.citation.titleCellular and Molecular Life Sciences-
dc.citation.number22-
dc.citation.endPage2885-
dc.citation.startPage2878-
dc.citation.volume61-
dc.contributor.affiliatedAuthorWon Gon Kim-
dc.contributor.affiliatedAuthorIn Ja Ryoo-
dc.contributor.affiliatedAuthorIck Dong Yoo-
dc.contributor.alternativeNamePark-
dc.contributor.alternativeNameKim-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName류인자-
dc.contributor.alternativeNameLee-
dc.contributor.alternativeNameHuh-
dc.contributor.alternativeNameYoun-
dc.contributor.alternativeName유익동-
dc.contributor.alternativeNamePark-
dc.identifier.bibliographicCitationCellular and Molecular Life Sciences, vol. 61, no. 22, pp. 2878-2885-
dc.identifier.doi10.1007/s00018-004-4341-3-
dc.subject.keywordERK-
dc.subject.keywordmelanogenesis-
dc.subject.keywordMITF-
dc.subject.keywordterrein-
dc.subject.keywordtyrosinase-
dc.subject.localERK-
dc.subject.localErk-
dc.subject.localmelanogenesis-
dc.subject.localMelanogenesis-
dc.subject.localmicrophthalmia-associated transcription factor (MITF)-
dc.subject.localMITF-
dc.subject.localMITF(microphthalmia transcription factor)-
dc.subject.localMitf-
dc.subject.localTerrein-
dc.subject.localterrein-
dc.subject.localTyrosinase-
dc.subject.localtyrosinase-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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