Nervonoylceramide (C24:1Cer), a lipid biomarker for ocular irritants released from the 3D reconstructed human cornea-like epithelium, MCTT HCE™

被引:9
|
作者
Lee, Miri [1 ]
Joo, Kyung-Mi [2 ]
Choi, Seunghye [1 ]
Lee, Su-Hyon [3 ]
Kim, Seol Yeong [3 ]
Chun, Young-Jin [4 ]
Choi, Dalwoong [5 ]
Lim, Kyung-Min [1 ]
机构
[1] Ewha Womans Univ, Coll Pharm, 52 Ewhayeodae Gil, Seoul 03760, South Korea
[2] AMOREPACIFIC Corp, R&D Ctr, Yongin 17074, South Korea
[3] Biosolution Co, Seoul 101811, South Korea
[4] Chung Ang Univ, Coll Pharm, Seoul 06974, South Korea
[5] Korea Univ, Grad Sch, Dept Publ Hlth Sci, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
Eye irritation; 3D reconstructed human cornea-like epithelium; Lipidomics; Nervonoylceramide C24:1 ceramide; MESSENGER-RNA EXPRESSION; EYE IRRITATION; SUBSTRATE-SPECIFICITY; METABOLIZING ENZYMES; AMNIOTIC MEMBRANE; GENE-EXPRESSION; TIGHT JUNCTIONS; CELLS; MODEL; CHEMICALS;
D O I
10.1016/j.tiv.2017.11.008
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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 (TM) 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 (TM) 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.
引用
收藏
页码:94 / 102
页数:9
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