http://purl.uniprot.org/citations/19740627 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/19740627 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundToll-like receptors (TLRs) recognize pathogen-associated molecular patterns (PAMPs), which have been evolutionarily conserved in microbes. Human melanocytes are not simply pigment-producing cells but also have the phagocytic capacity and can produce pro-inflammatory mediators. However, the mechanisms of recognition of microbes by melanocytes have not yet been fully established.ObjectiveWe investigated the TLRs 1-10 expression profile in human epidermal melanocytes and assessed their functions after triggering by their specific ligands.MethodsTLRs mRNA expression was determined by RT-PCR, and the TLR protein expression was measured by flow cytometry and immunofluorescence assays. After stimulation with various TLR ligands, the production of inflammatory cytokine IL-8 and IL-6 was measured by ELISA and the mRNA for chemokine CCL2, CCL3 and CCL5 was analyzed by real-time PCR. Phosphorylation of IkappaBalpha in TLR ligands-triggered melanocytes was determined by Western blot and the nucleus translocation of NF-kappaBp65 was analyzed by immunofluorescence.ResultsHuman melanocytes constitutively expressed TLRs 1-4, 6, 7 and 9 mRNA. Ample amounts of TLRs 2-4, 7 and 9 were confirmed at protein level. Stimulation of melanocytes with TLRs ligands resulted in the release of cytokines (IL-8 and IL-6) and the mRNA accumulation of chemokines (CCL2, CCL3 and CCL5). Triggering of TLRs in melanocytes resulted in the up-regulation of phosphorylated IkappaBalpha and in the nucleus translocation of NF-kappaBp65.ConclusionPresent study indicates human melanocytes express a panel of functional TLRs. The ligation of TLRs can turn these cells into active players of the skin innate immunity."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.org/dc/terms/identifier | "doi:10.1016/j.jdermsci.2009.08.003"xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/author | "Zhang S."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/author | "Xiang L."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/author | "Kang K."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/author | "Yu N."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/author | "Guan M."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/author | "Zuo F."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/date | "2009"xsd:gYear |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/name | "J Dermatol Sci"xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/pages | "113-120"xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/title | "Cultured human melanocytes express functional toll-like receptors 2-4, 7 and 9."xsd:string |
http://purl.uniprot.org/citations/19740627 | http://purl.uniprot.org/core/volume | "56"xsd:string |
http://purl.uniprot.org/citations/19740627 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/19740627 |
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http://purl.uniprot.org/uniprot/O15455#attribution-79E36D4FD6FC83B3BA545E9EA2C1B9AA | http://purl.uniprot.org/core/source | http://purl.uniprot.org/citations/19740627 |
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