College of Pharmacy, Ewha Womans University, Seoul 03760, Republic of Korea.
AMOREPACIFIC Corp. R&D Center, Yongin 17074, Republic of Korea.
Toxicol In Vitro. 2018 Mar;47:94-102. doi: 10.1016/j.tiv.2017.11.008. Epub 2017 Nov 15.
Due to invasive and painful procedures during in vivo rabbit eye irritation test, in vitro alternative methods have been widely investigated. Recently, 3D reconstructed human cornea-like epitheliums (RhCEs) garner a huge attention. RhCEs employ the tissue viability as a primary endpoint to determine ocular irritancy but additional biomarkers may improve its predictive capacity. Here, we explored lipid biomarkers for ocular irritants in MCTT HCE™ RhCE model. Three irritants; sodium lauryl sulfate, benzalkonium chloride and triton X-100 were selected to represent anionic, cationic and non-ionic detergent respectively. After treating MCTT HCE™ with irritants, the alteration of lipids in the treated tissues was examined with Nile Red staining, which revealed the depletion of corneal lipids. We further quantitated the release of ceramides and free fatty acids, major lipid components of cornea, into the medium during the post-treatment incubation, employing a sensitive UPLC-MS/MS method. Among 44 lipid species, nervonoylceramide (C24:1Cer) was found to be released commonly by all three irritants in a concentration-dependent manner. Tests with 10 additional reference substances further supported that C24:1Cer release was significantly correlated with viability. Examination of the genes involved in the biosynthetic pathway for C24:1Cer revealed that stearoylCoA desaturase (SCD) and elongase1 (ELOVL1) were upregulated, suggesting that lipids and related genes may be employed as biomarkers for ocular irritants.
由于在体内兔眼刺激性试验中存在侵入性和疼痛性操作,因此人们广泛研究了体外替代方法。最近,三维重建的人角膜样上皮(RhCE)引起了广泛关注。RhCE 将组织活力作为主要终点来确定眼部刺激性,但其他生物标志物可能会提高其预测能力。在这里,我们在 MCTT HCE™ RhCE 模型中探索了用于眼部刺激性的脂质生物标志物。选择三种刺激性物质:十二烷基硫酸钠、苯扎氯铵和 Triton X-100,分别代表阴离子、阳离子和非离子型清洁剂。用刺激性物质处理 MCTT HCE™后,用尼罗红染色检查处理组织中脂质的变化,结果显示角膜脂质减少。我们进一步使用灵敏的 UPLC-MS/MS 方法定量分析了在治疗后孵育过程中角膜主要脂质成分神经酰胺和游离脂肪酸释放到培养基中的情况。在 44 种脂质物种中,发现神经酰基神经酰胺(C24:1Cer)被三种刺激性物质共同以浓度依赖的方式释放。对另外 10 种参考物质的测试进一步支持 C24:1Cer 释放与活力显著相关。对 C24:1Cer 生物合成途径相关基因的检测表明,硬脂酰辅酶 A 去饱和酶(SCD)和延长酶 1(ELOVL1)上调,表明脂质和相关基因可作为眼部刺激性的生物标志物。