Department of Pathology, VU University Medical Centre, 1081 HV Amsterdam, The Netherlands.
Contact Dermatitis. 2013 Jun;68(6):331-8. doi: 10.1111/cod.12042.
Nickel was recently identified as a potent activator of dendritic cells through ligating with human Toll-like receptor (TLR)-4.
Here, we studied an extended panel of transition metals neighbouring nickel in the periodic table of elements, for their capacity to activate human monocyte-derived dendritic cells (MoDCs).
The panel included chromium, cobalt, and palladium, all of which are known to be frequent clinical sensitizers. MoDC activation was monitored by assessment of release of the pro-inflammatory mediator interleukin (IL)-8, a major downstream result of TLR ligation. Results The data obtained in the present study show that cobalt and palladium also have potent MoDC-activating capacities, whereas copper and zinc, but not iron and chromium, have low but distinct MoDC-activating potential. Involvement of endotoxin contamination in MoDC activation was excluded by Limulus assays and consistent stimulation in the presence of polymyxin B. The critical role of TLR4 in nickel-induced, cobalt-induced and palladium-induced activation was confirmed by essentially similar stimulatory patterns obtained in an HEK293 TLR4/MD2 transfectant cell line.
Given the adjuvant role of costimulatory danger signals, the development of contact allergies to the stimulatory metals may be facilitated by signals from direct TLR4 ligation, whereas other metal sensitizers, such as chromium, may rather depend on microbial or tissue-derived cofactors to induce clinical sensitization.
镍最近被鉴定为通过与人 Toll 样受体 (TLR)-4 结合来激活树突状细胞的有效激活剂。
在这里,我们研究了元素周期表中与镍相邻的一系列过渡金属,以研究它们激活人单核细胞来源的树突状细胞 (MoDC) 的能力。
该小组包括铬、钴和钯,它们都是已知的常见临床致敏剂。通过评估促炎介质白细胞介素 (IL)-8 的释放来监测 MoDC 的激活,这是 TLR 结合的主要下游结果。结果:本研究获得的数据表明,钴和钯也具有很强的 MoDC 激活能力,而铜和锌虽然没有明显的 MoDC 激活能力,但具有低但明显的 MoDC 激活潜力。通过鲎试验排除了内毒素污染对 MoDC 激活的参与,并且在多粘菌素 B 存在下一致刺激。在 HEK293 TLR4/MD2 转染细胞系中获得的基本相似的刺激模式证实了 TLR4 在镍诱导、钴诱导和钯诱导激活中的关键作用。
鉴于共刺激危险信号的佐剂作用,与刺激性金属接触过敏的发展可能会因直接 TLR4 结合的信号而得到促进,而其他金属致敏剂(如铬)可能更依赖于微生物或组织衍生的辅助因子来诱导临床致敏。