Oklahoma Center for Respiratory and Infectious Diseases, Oklahoma State University, Stillwater, OK, 74078, USA.
Department of Physiological Sciences, Lundberg-Kienlen Lung Biology and Toxicology Laboratory, Oklahoma State University, Stillwater, OK, 74078, USA.
Sci Rep. 2018 Feb 9;8(1):2709. doi: 10.1038/s41598-018-21073-x.
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and typically fatal lung disease with a very low survival rate. Excess accumulation of fibroblasts, myofibroblasts and extracellular matrix creates hypoxic conditions within the lungs, causing asphyxiation. Hypoxia is, therefore, one of the prominent features of IPF. However, there have been few studies concerning the effects of hypoxia on pulmonary fibroblasts. In this study, we investigated the molecular mechanisms of hypoxia-induced lung fibroblast proliferation. Hypoxia increased the proliferation of normal human pulmonary fibroblasts and IPF fibroblasts after exposure for 3-6 days. Cell cycle analysis demonstrated that hypoxia promoted the G1/S phase transition. Hypoxia downregulated cyclin D1 and A2 levels, while it upregulated cyclin E1 protein levels. However, hypoxia had no effect on the protein expression levels of cyclin-dependent kinase 2, 4, and 6. Chemical inhibition of hypoxia-inducible factor (HIF)-2 reduced hypoxia-induced fibroblast proliferation. Moreover, silencing of Nuclear Factor Activated T cell (NFAT) c2 attenuated the hypoxia-mediated fibroblasts proliferation. Hypoxia also induced the nuclear translocation of NFATc2, as determined by immunofluorescence staining. NFAT reporter assays showed that hypoxia-induced NFAT signaling activation is dependent on HIF-2, but not HIF-1. Furthermore, the inhibition or silencing of HIF-2, but not HIF-1, reduced the hypoxia-mediated NFATc2 nuclear translocation. Our studies suggest that hypoxia induces the proliferation of human pulmonary fibroblasts through NFAT signaling and HIF-2.
特发性肺纤维化(IPF)是一种慢性、进行性且通常致命的肺部疾病,存活率极低。成纤维细胞、肌成纤维细胞和细胞外基质的过度积累导致肺部缺氧,引起窒息。因此,缺氧是 IPF 的突出特征之一。然而,关于缺氧对肺成纤维细胞的影响的研究很少。在这项研究中,我们研究了缺氧诱导肺成纤维细胞增殖的分子机制。低氧培养 3-6 天后,正常的人肺成纤维细胞和 IPF 成纤维细胞的增殖增加。细胞周期分析表明,低氧促进 G1/S 期转变。低氧下调 cyclin D1 和 A2 水平,而上调 cyclin E1 蛋白水平。然而,低氧对 cyclin 依赖性激酶 2、4 和 6 的蛋白表达水平没有影响。化学抑制缺氧诱导因子(HIF)-2 降低了低氧诱导的成纤维细胞增殖。此外,沉默核因子活化 T 细胞(NFAT)c2 减弱了低氧介导的成纤维细胞增殖。免疫荧光染色显示,低氧还诱导 NFATc2 的核转位。NFAT 报告基因分析表明,低氧诱导的 NFAT 信号激活依赖于 HIF-2,但不依赖于 HIF-1。此外,HIF-2 的抑制或沉默,而不是 HIF-1 的抑制或沉默,降低了低氧介导的 NFATc2 核转位。我们的研究表明,缺氧通过 NFAT 信号和 HIF-2 诱导人肺成纤维细胞的增殖。