Ahn Joo Hee, Park Tae Jun, Jin Sun Hee, Kang Hee Young
Department of Dermatology, Ajou University School of Medicine, Suwon, Korea.
Exp Dermatol. 2008 May;17(5):412-7. doi: 10.1111/j.1600-0625.2008.00701.x.
Melanocytes are not simply pigment-producing cells, but produce substances with a range of biological functions including antimicrobial defense. Recent studies suggest that Toll-like receptors (TLRs) play an important role in the cellular response through the recognition of pathogens.
To investigate whether TLR4 and their adapter molecules are expressed in human melanocytes. The regulation and functional role of TLR4 on cell activation were also investigated.
The expression of TLR4 in human melanocytes was determined by using reverse transcription polymerase chain reaction, western blotting, immunochemistry and flow cytometry. In vivo expression of TLR4 in melanocytes of normal human epidermis was detected by immunohistochemical double staining. The effects of gram-negative bacterial derived lipopolysaccharide (LPS) on pigmentation were investigated with the measurement of melanin content.
TLR4 and its adaptor molecule CD14 and myeloid differentiation protein gene (MyD88) were constitutively expressed in cultured human melanocytes. Co-staining of histological human skin sections with TLR4 and a melanocyte marker, gp100, confirmed the expression of TLR4 in melanocytes under physiological conditions. LPS upregulated the expression of TLR4 and MyD88 and induced NF-kappaB nuclear translocation B nuclear translocation in melanocytes. Treatment of LPS increased pigmentation of human melanocytes.
We demonstrated that functional TLR4 was expressed in human melanocytes. Our findings suggest that TLR4 may play a role in microbial-induced melanogenesis.
黑素细胞并非仅仅是产生色素的细胞,还能产生具有一系列生物学功能的物质,包括抗菌防御。近期研究表明,Toll样受体(TLRs)通过识别病原体在细胞反应中发挥重要作用。
研究TLR4及其衔接分子在人黑素细胞中是否表达。同时研究TLR4对细胞活化的调控及其功能作用。
采用逆转录聚合酶链反应、蛋白质免疫印迹法、免疫化学和流式细胞术检测人黑素细胞中TLR4的表达。通过免疫组织化学双重染色检测正常人表皮黑素细胞中TLR4的体内表达。通过测量黑色素含量研究革兰氏阴性菌衍生的脂多糖(LPS)对色素沉着的影响。
TLR4及其衔接分子CD14和髓样分化蛋白基因(MyD88)在培养的人黑素细胞中组成性表达。用TLR4和黑素细胞标志物gp100对人皮肤组织切片进行共染色,证实了在生理条件下黑素细胞中TLR4的表达。LPS上调了黑素细胞中TLR4和MyD88的表达,并诱导核因子κB(NF-κB)核转位。LPS处理增加了人黑素细胞的色素沉着。
我们证明功能性TLR4在人黑素细胞中表达。我们的研究结果表明,TLR4可能在微生物诱导的黑素生成中起作用。