The inhibition of melanogenesis via the PKA and ERK signaling pathways by Chlamydomonas reinhardtii extract in B16F10 melanoma cells and artificial human skin equivalents

Cited 27 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorA Lee-
dc.contributor.authorJ Y Kim-
dc.contributor.authorJina Heo-
dc.contributor.authorDae Hyun Cho-
dc.contributor.authorHee-Sik Kim-
dc.contributor.authorI S An-
dc.contributor.authorS An-
dc.contributor.authorS Bae-
dc.date.accessioned2019-01-23T16:31:13Z-
dc.date.available2019-01-23T16:31:13Z-
dc.date.issued2018-
dc.identifier.issn1017-7825-
dc.identifier.uri10.4014/jmb.1810.10008ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18300-
dc.description.abstractAbnormal melanin synthesis results in several hyperpigmentary disorders such as freckles, melanoderma, age spots, and other hyperpigmentation syndromes. In this study, we investigated the anti-melanogenic effects of an extract from the microalgae Chlamydomonas reinhardtii (CE) and potential mechanisms responsible for its inhibitory effect in B16F10, normal human epidermal melanocyte cells, and human skin-equivalent models. The CE extract showed significant dose-dependent inhibitory effects on α-melanocyte-stimulating hormone-induced melanin synthesis in cells. Additionally, the CE extract exhibited suppressive effects on the mRNA and protein expression of microphthalmia-associated transcription factor, tyrosinase, tyrosinase-related protein-1, and tyrosinase-related protein-2. The CE extract also inhibited the phosphorylation of protein kinase A and extracellular signal-related kinase, which function as upstream regulators of melanogenesis. Using a three-dimensional reconstructed pigmented epidermis model, the CE-mediated anti-pigmentation effects were confirmed by Fontana-Masson staining and melanin content assays. Taken together, CE extract can be used as an anti-pigmentation agent.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleThe inhibition of melanogenesis via the PKA and ERK signaling pathways by Chlamydomonas reinhardtii extract in B16F10 melanoma cells and artificial human skin equivalents-
dc.title.alternativeThe inhibition of melanogenesis via the PKA and ERK signaling pathways by Chlamydomonas reinhardtii extract in B16F10 melanoma cells and artificial human skin equivalents-
dc.typeArticle-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.number12-
dc.citation.endPage2132-
dc.citation.startPage2121-
dc.citation.volume28-
dc.contributor.affiliatedAuthorJina Heo-
dc.contributor.affiliatedAuthorDae Hyun Cho-
dc.contributor.affiliatedAuthorHee-Sik Kim-
dc.contributor.alternativeName이아영-
dc.contributor.alternativeName김지예-
dc.contributor.alternativeName허진아-
dc.contributor.alternativeName조대현-
dc.contributor.alternativeName김희식-
dc.contributor.alternativeName안인숙-
dc.contributor.alternativeName안성관-
dc.contributor.alternativeName배승희-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, vol. 28, no. 12, pp. 2121-2132-
dc.identifier.doi10.4014/jmb.1810.10008-
dc.subject.keywordAnti-pigmentation-
dc.subject.keywordCell culture-
dc.subject.keywordChlamydomonas reinhardtii-
dc.subject.keywordHuman skin equivalents-
dc.subject.keywordMelanin-
dc.subject.localAnti-pigmentation-
dc.subject.localCell culture-
dc.subject.localcell culture-
dc.subject.localCell Culture-
dc.subject.localCell cultures-
dc.subject.localChlamydomonas reinhardtii-
dc.subject.localchlamydomonas reinhardtii-
dc.subject.localHuman skin equivalents-
dc.subject.localmelanin-
dc.subject.localMelanin-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Cell Factory Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.