Zhu Chengpeng, Pan Fangyu, Ge Lianping, Zhou Jing, Chen Longlong, Zhou Tong, Zong Rongrong, Xiao Xinye, Dong Nuo, Yang Maomin, Ma Jian-Xing, Liu Zuguo, Zhou Yueping
Eye Institute of Xiamen University, Fujian Provincial Key Laboratory of Ophthalmology and Visual Science, Xiamen, Fujian, China.
Affiliated Xiamen Eye Center of Xiamen University, Xiamen, Fujian, China.
PLoS One. 2014 Oct 8;9(10):e108859. doi: 10.1371/journal.pone.0108859. eCollection 2014.
We recently demonstrated that SERPINA3K, a serine proteinase inhibitor, has antioxidant activity in the cornea. Here we investigated the antioxidant effects of SERPINA3K on the pterygial, which is partially caused by oxidative stress in pathogenesis. The head part of primary pterygial tissue was dissected and then cultured in keratinocyte serum-free defined medium (KSFM). The cultured pterygial epithelial cells (PECs) were treated with SERPINA3K. The cell proliferation and migration of PECs were measured and analyzed. Western blot and quantitative real-time polymerase chain reaction (PCR) assay were performed. It showed that SERPINA3K significantly suppressed the cell proliferation of PECs in a concentration-dependent manner, compared with cultured human conjunctival epithelial cells. SERPINA3K also inhibited the cell migration of PECs. Towards its underlying mechanism, SERPINA3K had antioxidant activities on the PECs by significantly inhibiting NADPH oxidase 4 (NOX4), which is an important enzyme of ROS generation, and by elevating the levels of key antioxidant factors of ROS: such as NAD(P)H dehydrogenase (quinone 1) (NQO1), NF-E2-related factor-2 (NRF2) and superoxide dismutases (SOD2). Meanwhile, SERPINA3K down-regulated the key effectors of Wnt signaling pathway: β-catenin, nonphospho-β-catenin, and low-density lipoprotein receptor-related protein 6 (LRP6). We provided novel evidence that SERPINA3K had inhibitory effects on pterygium and SERPINA3K played antioxidant role via regulating the ROS system and antioxidants.
我们最近证明,丝氨酸蛋白酶抑制剂SERPINA3K在角膜中具有抗氧化活性。在此,我们研究了SERPINA3K对翼状胬肉的抗氧化作用,翼状胬肉在发病机制中部分是由氧化应激引起的。解剖原发性翼状胬肉组织的头部,然后在角质形成细胞无血清限定培养基(KSFM)中培养。用SERPINA3K处理培养的翼状胬肉上皮细胞(PEC)。测量并分析PEC的细胞增殖和迁移。进行蛋白质免疫印迹和定量实时聚合酶链反应(PCR)分析。结果表明,与培养的人结膜上皮细胞相比,SERPINA3K以浓度依赖性方式显著抑制PEC的细胞增殖。SERPINA3K还抑制了PEC的细胞迁移。关于其潜在机制,SERPINA3K通过显著抑制NADPH氧化酶4(NOX4,活性氧生成的一种重要酶)以及提高活性氧关键抗氧化因子的水平,如NAD(P)H脱氢酶(醌1)(NQO1)、NF-E2相关因子2(NRF2)和超氧化物歧化酶(SOD2),从而对PEC具有抗氧化活性。同时,SERPINA3K下调了Wnt信号通路的关键效应分子:β-连环蛋白、非磷酸化β-连环蛋白和低密度脂蛋白受体相关蛋白6(LRP6)。我们提供了新的证据,表明SERPINA3K对翼状胬肉具有抑制作用,并且SERPINA3K通过调节活性氧系统和抗氧化剂发挥抗氧化作用。