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Activation of Toll-like Receptors 1, 2, 4, 5, and 7 on Human Melanocytes Modulate Pigmentation.

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dc.contributor.authorJin, SH-
dc.contributor.authorKang, HY-
dc.date.accessioned2011-05-26T05:05:26Z-
dc.date.available2011-05-26T05:05:26Z-
dc.date.issued2010-
dc.identifier.issn1013-9087-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/2698-
dc.description.abstractHuman melanocytes are not simply pigment-producing cells. It may be part of the inflammatory response, during which the pigmentary system may produce more melanin or suppress melanization. Toll-like receptors (TLRs) have been implicated in both innate host defense against pathogens and inflammatory response. Therefore, it may be possible that activation of TLRs in melanocytes may play a role in the modulation of melanogenesis. In this study, we investigated whether normal human melanocytes expressed TLRs and analyzed pigmentation changes upon TLR stimulation. The expression of TLR1~10 mRNA in cultured human melanocyte was analyzed using RT-PCR, Western blotting and immunocytochemistry. Human melanocytes constitutively express mRNA and protein for TLR2, 3, 4, 5, 7, 9 and 10. Stimulation of TLR1/2 and 4 with Pam3CSK4 and lipopolysaccharide induced pigmentation of melanocytes. Activation of TLR5 and 7 with flagellin and imiquimod treatments reduced pigmentation of melanocytes and zebrafish. In summary, the results provided evidence for TLRs expression in normal human melanocytes. It is speculated that a response of melanocyte to TLR ligands may play a role in the pigmentary change in the skin.-
dc.language.isoen-
dc.titleActivation of Toll-like Receptors 1, 2, 4, 5, and 7 on Human Melanocytes Modulate Pigmentation.-
dc.typeArticle-
dc.identifier.pmid21165228-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991735/-
dc.contributor.affiliatedAuthor강, 희영-
dc.type.localJournal Papers-
dc.identifier.doi10.5021/ad.2010.22.4.486-
dc.citation.titleAnnals of dermatology-
dc.citation.volume22-
dc.citation.number4-
dc.citation.date2010-
dc.citation.startPage486-
dc.citation.endPage489-
dc.identifier.bibliographicCitationAnnals of dermatology, 22(4). : 486-489, 2010-
dc.identifier.eissn2005-3894-
dc.relation.journalidJ010139087-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Dermatology
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