Literature DB >> 15558216

Terrein: a new melanogenesis inhibitor and its mechanism.

S-H Park1, D-S Kim, W-G Kim, I-J Ryoo, D-H Lee, C-H Huh, S-W Youn, I-D Yoo, K-C Park.   

Abstract

Terrein 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 microM) 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.

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Year:  2004        PMID: 15558216     DOI: 10.1007/s00018-004-4341-3

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  62 in total

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  29 in total

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Journal:  World J Microbiol Biotechnol       Date:  2017-02-27       Impact factor: 3.312

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6.  Improving the yield of (+)-terrein from the salt-tolerant Aspergillus terreus PT06-2.

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8.  Enhanced production of (+)-terrein in fed-batch cultivation of Aspergillus terreus strain PF26 with sodium citrate.

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9.  Genetic and Histopathological Alterations in Caco-2 and HuH-7 Cells Treated with Secondary Metabolites of Marine fungi.

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10.  Topical hypopigmenting agents for pigmentary disorders and their mechanisms of action.

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