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Activation of Toll-like Receptors 1, 2, 4, 5, and 7 on Human Melanocytes Modulate Pigmentation
Annals of Dermatology ; : 486-489, 2010.
Artículo en Inglés | WPRIM | ID: wpr-189830
ABSTRACT
Human 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.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Piel / Pez Cebra / Pigmentación / ARN Mensajero / Inmunohistoquímica / Western Blotting / Receptores Toll-Like / Flagelina / Aminoquinolinas / Ligandos Límite: Humanos Idioma: Inglés Revista: Annals of Dermatology Año: 2010 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Piel / Pez Cebra / Pigmentación / ARN Mensajero / Inmunohistoquímica / Western Blotting / Receptores Toll-Like / Flagelina / Aminoquinolinas / Ligandos Límite: Humanos Idioma: Inglés Revista: Annals of Dermatology Año: 2010 Tipo del documento: Artículo