Wang Xin, Dai Wujing, Wang Yanrang, Gu Qing, Yang Deyi, Zhang Ming
Tianjin Center for Disease Control and Prevention, Tianjin 300011, China.
College of Public Health, Tianjin Medical University, Tianjin 300070, China.
Int J Environ Res Public Health. 2015 Sep 1;12(9):10739-54. doi: 10.3390/ijerph120910739.
Silicosis is a form of occupational lung disease caused by inhalation of crystalline silica dust. While the pathogenesis of silicosis is not clearly understood, the Wnt/β-catenin signaling pathway is thought to play a major role in lung fibrosis. To explore the role of Wnt/β-catenin pathway in silicosis, we blocked Wnt/β-catenin pathway both in silica-treated MLE-12 cells (a mouse pulmonary epithelial cell line) and in a mouse silicosis model by using a lentiviral vector expressing a short hairpin RNA silencing β-catenin (Lv-shβ-catenin). In vitro, Lv-shβ-catenin significantly decreased the expression of β-catenin, MMP2 and MMP9, and secretion of TGF-β1. In vivo, intratracheal treatment with Lv-shβ-catenin significantly reduced expression of β-catenin in the lung and levels of TGF-β1 in bronchoalveolar lavage fluid, and notably attenuated pulmonary fibrosis as evidenced by hydroxyproline content and collagen I\III synthesis in silica-administered mice. These results indicate that blockade of the Wnt/β-catenin pathway can prevent the development of silica-induced lung fibrosis. Thus Wnt/β-catenin pathway may be a target in prevention and treatment of silicosis.
矽肺是一种因吸入结晶二氧化硅粉尘而导致的职业性肺病。虽然矽肺的发病机制尚不清楚,但Wnt/β-连环蛋白信号通路被认为在肺纤维化中起主要作用。为了探究Wnt/β-连环蛋白通路在矽肺中的作用,我们通过使用表达短发夹RNA沉默β-连环蛋白的慢病毒载体(Lv-shβ-连环蛋白),在二氧化硅处理的MLE-12细胞(一种小鼠肺上皮细胞系)和小鼠矽肺模型中阻断Wnt/β-连环蛋白通路。在体外,Lv-shβ-连环蛋白显著降低了β-连环蛋白、MMP2和MMP9的表达以及TGF-β1的分泌。在体内,气管内给予Lv-shβ-连环蛋白显著降低了肺中β-连环蛋白的表达以及支气管肺泡灌洗液中TGF-β1的水平,并且显著减轻了肺纤维化,这在给予二氧化硅的小鼠中通过羟脯氨酸含量和I/III型胶原蛋白合成得以证明。这些结果表明,阻断Wnt/β-连环蛋白通路可以预防二氧化硅诱导的肺纤维化的发展。因此,Wnt/β-连环蛋白通路可能是矽肺防治的一个靶点。