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Globular adiponectin acts as a melanogenic signal in human epidermal melanocytes

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dc.contributor.authorKim, Y.-
dc.contributor.authorCho, J. Y.-
dc.contributor.authorOh, S. W.-
dc.contributor.authorKang, M.-
dc.contributor.authorLee, S. E.-
dc.contributor.authorJung, E.-
dc.contributor.authorPark, Y. S.-
dc.contributor.authorLee, J.-
dc.date.accessioned2021-08-11T11:43:58Z-
dc.date.available2021-08-11T11:43:58Z-
dc.date.issued2018-09-
dc.identifier.issn0007-0963-
dc.identifier.issn1365-2133-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/5691-
dc.description.abstractBackgroundAdiponectin is an adipocyte-derived cytokine that circulates as a full-length protein and a fragment containing the globular domain of adiponectin (gAd). A recent study has reported the antimelanogenic effects of full-length adiponectin. ObjectivesTo examine the involvement of gAd in melanogenesis and its mechanisms of action. MethodsThe effects of gAd on melanogenesis and its mechanisms of action were investigated in human epidermal melanocytes and reconstructed epidermis, including melanin content, cellular tyrosinase activity, cyclic adenosine monophosphate (cAMP) production and protein kinase A (PKA) activity, expression and phosphorylation of signalling molecules. ResultsExogenous gAd increased melanin content, and the mRNA levels of microphthalmia-associated transcription factor (MITF) and its downstream genes TRP1, but not TRP2, were increased by gAd. However, cAMP production and PKA activity were not affected by gAd. Moreover, attempts to elucidate the underlying mechanism behind the gAd-mediated effect revealed that gAd could regulate melanogenesis by upregulating MITF through phosphorylation of the cAMP response element-binding protein (CREB). In addition, upregulation of MITF was mediated by activation of adenosine monophosphate-activated protein kinase (AMPK)-p38 mitogen-activated protein kinase (MAPK) signalling. Taken together, these findings indicate that promotion of melanogenesis by gAd occurs through increased expression of MITF, which is mediated by activation of the AMPK-p38 MAPK-CREB pathway. ConclusionsThese findings suggest that gAd contributes to epidermal homeostasis via its effect on melanocyte biology, and products of adipose tissue could affect epidermal biology.-
dc.format.extent13-
dc.language영어-
dc.language.isoENG-
dc.publisherBlackwell Publishing Inc.-
dc.titleGlobular adiponectin acts as a melanogenic signal in human epidermal melanocytes-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/bjd.16488-
dc.identifier.scopusid2-s2.0-85050941817-
dc.identifier.wosid000444673400037-
dc.identifier.bibliographicCitationBritish Journal of Dermatology, v.179, no.3, pp 689 - 701-
dc.citation.titleBritish Journal of Dermatology-
dc.citation.volume179-
dc.citation.number3-
dc.citation.startPage689-
dc.citation.endPage701-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaDermatology-
dc.relation.journalWebOfScienceCategoryDermatology-
dc.subject.keywordPlusACTIVATED PROTEIN-KINASE-
dc.subject.keywordPlusFATTY-ACID OXIDATION-
dc.subject.keywordPlusADIPOSE-SPECIFIC PROTEIN-
dc.subject.keywordPlusSKELETAL-MUSCLE CELLS-
dc.subject.keywordPlusDEFICIENT MICE-
dc.subject.keywordPlusGLUCOSE-UPTAKE-
dc.subject.keywordPlusAMP-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusOBESITY-
dc.subject.keywordPlusWEIGHT-
dc.subject.keywordAuthorAdiponectin-
dc.subject.keywordAuthormelanocyte-
dc.subject.keywordAuthorTRP1-
dc.subject.keywordAuthorPKA-
dc.subject.keywordAuthorCREB-
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