Laboratory of Toxicology, Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via Balzaretti 9, 20133 Milan, Italy.
Laboratory of Toxicology, Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via Balzaretti 9, 20133 Milan, Italy.
Toxicol In Vitro. 2020 Oct;68:104929. doi: 10.1016/j.tiv.2020.104929. Epub 2020 Jul 3.
In vitro approaches to address key events in chemical-induced skin sensitization have been developed, but there is still uncertain how they will be useful to predict the potency for an effective risk assessment. Keratinocytes (KCs) play a key role in all phases of skin sensitization. Dendritic cells (DCs) activation and maturation require the binding of cytokines produced by KC as a result of initial chemical exposure. We previously identified interleukin-18 (IL-18) as useful marker for determination of skin sensitization potential of chemicals. The aim of this paper was to mimic the interaction between KCs and DCs using a co-culture of NCTC 2544 and THP-1 cells. Three selected contact allergens of different potency (Bandrowski's base, diethyl maleate, and imidazolidinyl urea) were tested in time-course experiments (24, 48 and 72 h). Cell surface markers expression (CD80, CD86, and HLA-DR) was determined by flow cytometry analysis while IL-18 production was evaluated with specific sandwich ELISA. Results obtained from this simple in vitro co-culture system show the possibility to study the contribution of KCs in DCs activation through the analysis of HLA-DR expression. Results obtained demonstrate the ability of the KCs to favor the full maturation of the DCs in the presence of moderate and weak allergens, while the extreme allergen induced a complete maturation of DC alone without the need of KCs.
已经开发出了用于解决化学诱导性皮肤致敏关键事件的体外方法,但仍然不确定它们将如何有助于预测效力以进行有效的风险评估。角质形成细胞(KC)在皮肤致敏的所有阶段都起着关键作用。树突状细胞(DC)的激活和成熟需要 KC 产生的细胞因子的结合,这是由于初始化学暴露所致。我们之前确定白细胞介素-18(IL-18)是用于确定化学物质皮肤致敏潜力的有用标记物。本文的目的是使用 NCTC 2544 和 THP-1 细胞的共培养来模拟 KC 和 DC 之间的相互作用。三种不同效力的选择接触过敏原(班德罗夫斯基碱,马来酸二乙酯和咪唑烷基脲)在时间过程实验中(24、48 和 72 小时)进行了测试。通过流式细胞术分析测定细胞表面标志物表达(CD80、CD86 和 HLA-DR),并用特异性夹心 ELISA 评估 IL-18 产生。从这种简单的体外共培养系统获得的结果表明,通过分析 HLA-DR 表达,有可能研究 KC 在 DC 激活中的贡献。结果表明,在存在中度和弱变应原的情况下,KC 能够促进 DC 的完全成熟,而极端变应原则无需 KC 即可单独诱导 DC 的完全成熟。