Ju Hee-Jung, Byun Yong-Soo, Mok Jee-Won, Joo Choun-Ki
Catholic Institute for Visual Science, Seoul St. Mary's Hospital, Seoul 06591, Republic of Korea.
Catholic Institute for Visual Science, Seoul St. Mary's Hospital, Seoul 06591, Republic of Korea; Department of Ophthalmology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
J Ophthalmol. 2016;2016:8350134. doi: 10.1155/2016/8350134. Epub 2016 Jul 31.
To determine the effect of hyperosmolarity on cell survival/apoptosis of conjunctival epithelial cells and evaluate the possible role of IL6, Wong-Kilbourne derivative of Chang conjunctival cell line (WKD) was used in this study. Confluent cells were incubated under different osmolarity (290 mOsm and 500 mOsm) with or without neutralizing IL6 antibody (50 ng/mL). The expression of IL6 level was measured in the supernatant of each conditioned medium. Cell viability/apoptosis assay was performed using Annexin V/Propidium Iodide (PI) and Cell Counting Kit-8 (CCK-8). Western blot was conducted to measure the abundance of apoptotic markers and IL6 related downstream signaling pathway. The concentration of IL6 showed time-dependent increase in cells treated with 500 mOsm. Although apoptosis of WKD cell is increased in treated 500 mOsm for 24 h, apoptosis reduced in WKD cell treated 500 mOsm with anti-IL6 for 24 h. Anti-IL6 inhibited the activation of JAK-STAT signaling pathway, which was induced by hyperosmolarity. Hyperosmolar condition induced apoptosis in conjunctival epithelial cells, along with increase of IL6 production. IL6 neutralizing antibody inhibited apoptosis and JAK-STAT signaling in hyperosmolar condition. These findings suggested that IL6 may be involved in apoptotic change and in hyperosmolarity.
为了确定高渗对结膜上皮细胞存活/凋亡的影响,并评估白细胞介素6(IL6)的可能作用,本研究使用了张氏结膜细胞系的黄-基尔伯恩衍生物(WKD)。将汇合的细胞在不同渗透压(290mOsm和500mOsm)下培养,添加或不添加中和性IL6抗体(50ng/mL)。在每种条件培养基的上清液中测量IL6水平的表达。使用膜联蛋白V/碘化丙啶(PI)和细胞计数试剂盒-8(CCK-8)进行细胞活力/凋亡检测。进行蛋白质免疫印迹法以测量凋亡标志物和IL6相关下游信号通路的丰度。在用500mOsm处理的细胞中,IL6的浓度呈时间依赖性增加。虽然在500mOsm处理24小时的WKD细胞中凋亡增加,但在500mOsm并用抗IL6处理24小时的WKD细胞中凋亡减少。抗IL6抑制了由高渗诱导的JAK-STAT信号通路的激活。高渗条件诱导结膜上皮细胞凋亡,同时IL6产生增加。IL6中和抗体在高渗条件下抑制凋亡和JAK-STAT信号传导。这些发现表明IL6可能参与凋亡变化和高渗过程。