Szameit S, Vierlinger K, Farmer L, Tuschl H, Noehammer C
Toxicology, Austrian Research Centers GmbH-ARC, Seibersdorf, Vienna, Austria.
Clin Exp Allergy. 2009 Jun;39(6):856-68. doi: 10.1111/j.1365-2222.2009.03222.x. Epub 2009 Mar 10.
The replacement of animal tests for the detection of the sensitizing potential of chemicals is of great importance due to current legislation. One promising approach for the development of an in vitro assay is the exposure of immature dendritic cells (iDCs) to contact sensitizers and irritants, followed by an analysis of the maturation status of the cells.
The aim of this study was to further investigate the performance of our previously developed targeted microarray, the immune toxicity chip. In addition, we aimed to identify new marker genes for the discrimination of allergens and irritants using whole-genome microarrays.
Monocyte-derived iDCs were exposed to contact sensitizers and irritants in concentrations resulting in 10-20% cytotoxicity, as determined by dose-response curves. Changes in gene expression were analysed using the immune toxicity chip and a commercially available whole-genome microarray.
Using the immune toxicity chip, we could identify a panel of marker genes suitable to discriminate strong allergens and irritants. Analysis with the whole-genome array revealed additional genes that are differentially expressed after allergen exposure, but not after irritant exposure. Hierarchical clustering of these genes showed distinct groups representing the different chemicals.
Here we show that our test system based on an immune-specific microarray is suitable for the discrimination of strong allergens and irritants. Genes detected as differentially expressed with the whole-genome array and previously not connected to the maturation process of DCs might be suitable candidate genes for the identification of weaker sensitizers.
鉴于当前的法规,替代动物试验以检测化学品的致敏潜力具有重要意义。开发体外试验的一种有前景的方法是将未成熟树突状细胞(iDCs)暴露于接触性致敏剂和刺激物,然后分析细胞的成熟状态。
本研究的目的是进一步研究我们之前开发的靶向微阵列——免疫毒性芯片的性能。此外,我们旨在使用全基因组微阵列鉴定用于区分过敏原和刺激物的新标记基因。
通过剂量反应曲线确定,将单核细胞衍生的iDCs暴露于导致10 - 20%细胞毒性的接触性致敏剂和刺激物浓度下。使用免疫毒性芯片和市售的全基因组微阵列分析基因表达的变化。
使用免疫毒性芯片,我们可以鉴定出一组适合区分强过敏原和刺激物的标记基因。全基因组阵列分析揭示了在过敏原暴露后差异表达但在刺激物暴露后不差异表达的其他基因。这些基因的层次聚类显示出代表不同化学品的不同组。
在这里我们表明,我们基于免疫特异性微阵列的测试系统适用于区分强过敏原和刺激物。通过全基因组阵列检测为差异表达且以前未与DCs成熟过程相关的基因可能是鉴定较弱致敏剂的合适候选基因。