Zorn-Kruppa Michaela, Houdek Pia, Wladykowski Ewa, Engelke Maria, Bartok Melinda, Mewes Karsten R, Moll Ingrid, Brandner Johanna M
University Medical Center Hamburg-Eppendorf, Department of Dermatology and Venerology, 20246 Hamburg, Germany.
Jacobs University Bremen gGmbH, School of Engineering and Sciences, 28759 Bremen, Germany.
PLoS One. 2014 Dec 10;9(12):e114181. doi: 10.1371/journal.pone.0114181. eCollection 2014.
The depth of injury (DOI) is a mechanistic correlate to the ocular irritation response. Attempts to quantitatively determine the DOI in alternative tests have been limited to ex vivo animal eyes by fluorescent staining for biomarkers of cell death and viability in histological cross sections. It was the purpose of this study to assess whether DOI could also be measured by means of cell viability detected by the MTT assay using 3-dimensional (3D) reconstructed models of cornea and conjunctiva. The formazan-free area of metabolically inactive cells in the tissue after topical substance application is used as the visible correlate of the DOI. Areas of metabolically active or inactive cells are quantitatively analyzed on cryosection images with ImageJ software analysis tools. By incorporating the total tissue thickness, the relative MTT-DOI (rMTT-DOI) was calculated. Using the rMTT-DOI and human reconstructed cornea equivalents, we developed a prediction model based on suitable viability cut-off values. We tested 25 chemicals that cover the whole range of eye irritation potential based on the globally harmonized system of classification and labelling of chemicals (GHS). Principally, the MTT-DOI test method allows distinguishing between the cytotoxic effects of the different chemicals in accordance with all 3 GHS categories for eye irritation. Although the prediction model is slightly over-predictive with respect to non-irritants, it promises to be highly valuable to discriminate between severe irritants (Cat. 1), and mild to moderate irritants (Cat. 2). We also tested 3D conjunctiva models with the aim to specifically address conjunctiva-damaging substances. Using the MTT-DOI method in this model delivers comparable results as the cornea model, but does not add additional information. However, the MTT-DOI method using reconstructed cornea models already provided good predictability that was superior to the already existing established in vitro/ex vivo methods.
损伤深度(DOI)是眼部刺激反应的一个机制相关指标。在替代试验中,通过对组织学横断面中细胞死亡和活力的生物标志物进行荧光染色,定量测定DOI的尝试仅限于离体动物眼睛。本研究的目的是评估是否也可以通过使用角膜和结膜的三维(3D)重建模型,通过MTT法检测细胞活力来测量DOI。局部应用物质后组织中代谢不活跃细胞的无色甲臜区域用作DOI的可见相关指标。使用ImageJ软件分析工具在冷冻切片图像上对代谢活跃或不活跃细胞的区域进行定量分析。通过纳入总组织厚度,计算相对MTT-DOI(rMTT-DOI)。使用rMTT-DOI和人重建角膜等效物,我们基于合适的活力临界值开发了一个预测模型。我们测试了25种根据全球化学品统一分类和标签制度(GHS)涵盖整个眼部刺激潜力范围的化学品。原则上,MTT-DOI测试方法能够根据GHS眼部刺激的所有3个类别区分不同化学品的细胞毒性作用。尽管预测模型对无刺激物的预测略有过度,但它有望在区分严重刺激物(第1类)和轻度至中度刺激物(第2类)方面具有很高的价值。我们还测试了3D结膜模型,旨在专门针对损害结膜的物质。在该模型中使用MTT-DOI方法产生的结果与角膜模型相当,但没有提供额外信息。然而,使用重建角膜模型的MTT-DOI方法已经提供了良好的可预测性,优于现有的体外/离体方法。