Li De-Quan, Luo Lihui, Chen Zhuo, Kim Hyun-Seung, Song Xiu Jun, Pflugfelder Stephen C
Ocular Surface Center, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, 6565 Fannin Street, NC-205, Houston, TX 77030, USA.
Exp Eye Res. 2006 Apr;82(4):588-96. doi: 10.1016/j.exer.2005.08.019. Epub 2005 Oct 3.
Hyperosmolarity has been recognized to be a pro-inflammatory stress to the corneal epithelium. The cell signalling pathways linking hyperosmolar stress and inflammation have not been well elucidated. This study investigated whether exposure of human limbal epithelial cells to hyperosmotic stress activates the mitogen-activated protein kinase (MAPK) pathways and induces production of pro-inflammatory cytokines, interleukin (IL) -1beta, tumor necrosis factor (TNF) alpha, and the C-X-C chemokine IL-8. Primary human limbal epithelial cultures in normal osmolar media (312 mOsM) were exposed to media with higher osmolarity (400-500 mOsM) by adding 50-90 mM NaCl, with or without SB202190, an inhibitor of c-Jun N-terminal kinases (JNK) pathway, PD 98059, an inhibitor of extracellular-regulated kinase (ERK) pathway, dexamethasone or doxycycline for different lengths of time. The conditioned media were collected after 24 hr of treatment for ELISA. Total RNA was extracted from cultures treated for 6 hr for semi-quantitative RT-PCR. Cells treated for 15-60 min were lysed in RIPA buffer and subjected to Western blot with phospho (p)-specific antibodies against p-JNK and p-ERK. The concentrations of IL-1beta, TNF-alpha and IL-8 proteins in 24 hr conditioned media of limbal epithelial cells progressively increased as the media osmolarity increased from 312 to 500 mOsM. Active p-JNK-1/p-JNK-2 and p-ERK-1/p-ERK-2 were detected by Western blot and peaked at 60 min in cells exposed to hyperosmolar media. The levels of p-JNK-1/p-JNK-2 and p-ERK1/p-ERK2 were positively correlated with the medium osmolarity. SB202190, PD98059 and doxycycline markedly suppressed the levels of p-JNK-1/p-JNK-2 and/or p-ERK1/p-ERK2, as well as IL-1beta, TNF-alpha and IL-8 mRNAs and proteins stimulated by hyperosmolar media. These findings provide direct evidence that hyperosmolarity induces inflammation in human limbal epithelial cells by increasing expression and production of pro-inflammatory cytokines and chemokines, a process that appears to be mediated through activation of the JNK and ERK MAPK signalling pathways. The efficacy of doxycycline in treating ocular surface diseases may be due to its ability to suppress JNK and ERK signalling activation and inflammatory mediator production in the limbal epithelium.
高渗已被认为是角膜上皮的一种促炎应激。连接高渗应激与炎症的细胞信号通路尚未得到充分阐明。本研究调查了人角膜缘上皮细胞暴露于高渗应激下是否会激活丝裂原活化蛋白激酶(MAPK)通路并诱导促炎细胞因子白细胞介素(IL)-1β、肿瘤坏死因子(TNF)α和C-X-C趋化因子IL-8的产生。通过添加50-90 mM氯化钠,将正常渗透压培养基(312 mOsM)中的原代人角膜缘上皮培养物暴露于渗透压更高的培养基(400-500 mOsM)中,分别添加或不添加c-Jun氨基末端激酶(JNK)通路抑制剂SB202190、细胞外调节激酶(ERK)通路抑制剂PD 98059、地塞米松或强力霉素,处理不同时长。处理24小时后收集条件培养基用于酶联免疫吸附测定(ELISA)。从处理6小时的培养物中提取总RNA用于半定量逆转录聚合酶链反应(RT-PCR)。将处理15-60分钟的细胞在RIPA缓冲液中裂解,并用针对磷酸化(p)-JNK和p-ERK的特异性抗体进行蛋白质免疫印迹法检测。随着培养基渗透压从312 mOsM增加到500 mOsM,角膜缘上皮细胞24小时条件培养基中IL-1β、TNF-α和IL-8蛋白的浓度逐渐增加。通过蛋白质免疫印迹法检测到活性p-JNK-1/p-JNK-2和p-ERK-1/p-ERK-2,在暴露于高渗培养基的细胞中60分钟时达到峰值。p-JNK-1/p-JNK-2和p-ERK1/p-ERK2的水平与培养基渗透压呈正相关。SB202190、PD98059和强力霉素显著抑制了高渗培养基刺激的p-JNK-1/p-JNK-2和/或p-ERK1/p-ERK2水平,以及IL-1β、TNF-α和IL-8的mRNA和蛋白水平。这些发现提供了直接证据,表明高渗通过增加促炎细胞因子和趋化因子的表达和产生来诱导人角膜缘上皮细胞炎症,这一过程似乎是通过JNK和ERK MAPK信号通路的激活介导的。强力霉素治疗眼表疾病的疗效可能归因于其抑制角膜缘上皮中JNK和ERK信号激活以及炎症介质产生的能力。