Chuang Eliseu Y, Li De-Quan, Bian Fang, Zheng Xiaofen, Pflugfelder Stephen C
Department of Ophthalmology, Ocular Surface Center, Cullen Eye Institute, Baylor College of Medicine, Houston, TX 77030, USA.
Eye Contact Lens. 2008 Sep;34(5):281-6. doi: 10.1097/ICL.0b013e3181842518.
To examine the effect of 4 commercially available contact lens multipurpose solutions (MPS) on the viability and barrier function of human corneal epithelial cells in vitro.
Immortalized human corneal epithelial cells were exposed to 4 solutions, MPS A, B, C, and D with culture medium and Hanks' Balanced Salt Solution as controls. MTT assay was used to evaluate cell viability. ApopTag Fluorescein Apoptosis assay was used to detect cell death in situ. Corneal epithelial barrier function was evaluated by fluorescein permeability and immunofluorescent staining for tight junction proteins zonula occludens (ZO)-1 and occludin.
Corneal epithelial survival rates, evaluated by MTT assay showed no statistical difference between MPS A and the culture medium or Hanks' Balanced Salt Solution controls. MPS B, C, and D were associated with significantly less cell survival than the controls after exposure for 6 hrs (all P<0.01). Compared with the controls, the MPS A did not increase cell apoptosis, whereas the other 3 caused higher apoptotic rates. The epithelial permeability after exposure to MPS A was similar to controls and significantly lower than MPS B and MPS D (P<0.01). The tight junction proteins ZO-1 and occludin were well maintained after exposure to MPS A. In contrast, the expression of ZO-1 and occludin were largely disturbed by the other 3 MPS solutions.
The current marketed contact lens MPS may have negative effects on human corneal epithelial viability and barrier function. Among 4 MPS studied, MPS A maintains the cell viability and barrier function significantly better than other 3 marketed products.
研究4种市售隐形眼镜多功能护理液(MPS)对人角膜上皮细胞体外活力及屏障功能的影响。
将永生化人角膜上皮细胞暴露于4种护理液(MPS A、B、C和D),以培养基和汉克斯平衡盐溶液作为对照。采用MTT法评估细胞活力。使用ApopTag荧光素凋亡检测法原位检测细胞死亡情况。通过荧光素通透性及紧密连接蛋白闭锁小带(ZO)-1和闭合蛋白的免疫荧光染色评估角膜上皮屏障功能。
MTT法评估的角膜上皮存活率显示,MPS A与培养基或汉克斯平衡盐溶液对照之间无统计学差异。暴露6小时后,MPS B、C和D与对照相比,细胞存活率显著降低(均P<0.01)。与对照相比,MPS A未增加细胞凋亡,而其他3种护理液导致更高的凋亡率。暴露于MPS A后的上皮通透性与对照相似,且显著低于MPS B和MPS D(P<0.01)。暴露于MPS A后,紧密连接蛋白ZO-1和闭合蛋白得到良好维持。相比之下,其他3种MPS溶液对ZO-1和闭合蛋白的表达造成了很大干扰。
目前市售的隐形眼镜MPS可能对人角膜上皮活力和屏障功能有负面影响。在所研究的4种MPS中,MPS A在维持细胞活力和屏障功能方面明显优于其他3种市售产品。