Batmunkh Rentsenkhand, Nishioka Yasuhiko, Aono Yoshinori, Azuma Momoyo, Kinoshita Katsuhiro, Kishi Jun, Makino Hideki, Kishi Masami, Takezaki Akio, Sone Saburo
Department of Respiratory Medicine and Rheumatology, University of Tokushima Graduate School, Tokushima, Japan.
J Med Invest. 2011 Aug;58(3-4):188-96. doi: 10.2152/jmi.58.188.
Idiopathic pulmonary fibrosis is a progressive and lethal disease of the lung that is characterized by the proliferation of fibroblasts and increased deposition of the extracellular matrix. The CCN6/WISP-3 is a member of the CCN family of matricellular proteins, which consists of six members that are involved in many vital biological functions. However, the regulation of lung fibroblasts mediated by CCN6 protein has not been fully elucidated. Here, we demonstrated that CCN6 induced the proliferation of lung fibroblasts by binding to integrin β1, leading to the phosphorylation of FAK(Y397). Furthermore, CCN6 showed a weak, but significant, ability to stimulate the expression of fibronectin. CCN6 was highly expressed in the lung tissues of mice treated with bleomycin. Our results suggest that CCN6 plays a role in the fibrogenesis of the lungs mainly by stimulating the growth of lung fibroblasts and is a potential target for the treatment of pulmonary fibrosis.
特发性肺纤维化是一种进行性致死性肺部疾病,其特征为成纤维细胞增殖和细胞外基质沉积增加。CCN6/WISP-3是基质细胞蛋白CCN家族的成员,该家族由六个成员组成,参与许多重要的生物学功能。然而,CCN6蛋白介导的肺成纤维细胞调节尚未完全阐明。在此,我们证明CCN6通过与整合素β1结合诱导肺成纤维细胞增殖,导致FAK(Y397)磷酸化。此外,CCN6显示出较弱但显著的刺激纤连蛋白表达的能力。CCN6在博莱霉素处理的小鼠肺组织中高表达。我们的结果表明,CCN6主要通过刺激肺成纤维细胞生长在肺纤维化形成中起作用,是治疗肺纤维化的潜在靶点。