Sanders Yan Y, Pardo Annie, Selman Moisés, Nuovo Gerard J, Tollefsbol Trygve O, Siegal Gene P, Hagood James S
Department of Pediatrics, Division of Pulmonary Medicine, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Am J Respir Cell Mol Biol. 2008 Nov;39(5):610-8. doi: 10.1165/rcmb.2007-0322OC. Epub 2008 Jun 12.
Mechanisms regulating myofibroblastic differentiation of fibroblasts within fibroblastic foci in idiopathic pulmonary fibrosis (IPF) remain unclear. Epigenetic processes, including DNA methylation, produce heritable but potentially reversible changes in DNA or its associated proteins and are prominent in development and oncogenesis. We have shown that Thy-1 suppresses myofibroblastic differentiation of lung fibroblasts and that fibroblasts in fibroblastic foci are Thy-1(-). Epigenetic down-regulation of Thy-1 has been demonstrated in cellular transformation and clinical cancer. We hypothesized that epigenetic regulation of Thy-1 affects the lung fibroblast fibrogenic phenotype. RT-PCR, methylation-specific PCR (MSP), and bisulfite genomic sequencing were used to determine the methylation status of the Thy-1 promoter in Thy-1(+) and Thy-1(-) lung fibroblasts, and MSP-in situ hybridization (MSPISH) was performed on fibrotic tissue. Thy-1 gene expression is absent in Thy-1(-) human and rat fibroblasts despite intact Thy-1 genomic DNA. Cytosine-guanine islands in the Thy-1 gene promoter are hypermethylated in Thy-1(-), but not Thy-1(+), fibroblasts. RT-PCR and MSP demonstrate that, in IPF samples in which Thy-1 expression is absent, the Thy-1 promoter region is methylated, whereas in lung samples retaining Thy-1 expression, the promoter region is unmethylated. MSPISH confirms methylation of the Thy-1 promoter in fibroblastic foci in IPF. Treatment with DNA methyltransferase inhibitors restores Thy-1 expression in Thy-1(-) fibroblasts. Epigenetic regulation of Thy-1 is a novel and potentially reversible mechanism in fibrosis that may offer the possibility of new therapeutic options.
特发性肺纤维化(IPF)中纤维母细胞灶内成纤维细胞向肌成纤维细胞分化的调控机制仍不清楚。包括DNA甲基化在内的表观遗传过程会在DNA或其相关蛋白质中产生可遗传但可能可逆的变化,并且在发育和肿瘤发生过程中很突出。我们已经表明,Thy-1抑制肺成纤维细胞向肌成纤维细胞的分化,并且纤维母细胞灶中的成纤维细胞是Thy-1阴性的。Thy-1的表观遗传下调已在细胞转化和临床癌症中得到证实。我们假设Thy-1的表观遗传调控会影响肺成纤维细胞的纤维化表型。使用逆转录聚合酶链反应(RT-PCR)、甲基化特异性PCR(MSP)和亚硫酸氢盐基因组测序来确定Thy-1阳性和阴性肺成纤维细胞中Thy-1启动子的甲基化状态,并对纤维化组织进行MSP原位杂交(MSPISH)。尽管Thy-1基因组DNA完整,但Thy-1阴性的人和大鼠成纤维细胞中不存在Thy-1基因表达。Thy-1基因启动子中的胞嘧啶-鸟嘌呤岛在Thy-1阴性成纤维细胞中高度甲基化,而在Thy-1阳性成纤维细胞中未甲基化。RT-PCR和MSP表明,在缺乏Thy-1表达的IPF样本中,Thy-1启动子区域甲基化,而在保留Thy-1表达的肺样本中,启动子区域未甲基化。MSPISH证实IPF中纤维母细胞灶内Thy-1启动子的甲基化。用DNA甲基转移酶抑制剂处理可恢复Thy-1阴性成纤维细胞中Thy-1的表达。Thy-1的表观遗传调控是纤维化中一种新的且可能可逆的机制,这可能为新的治疗选择提供可能性。