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Epigenetic regulation of Thy-1 gene expression by histone modification is involved in lipopolysaccharide-induced lung fibroblast proliferation

机译:通过组蛋白修饰对Thy-1基因表达的表观遗传调控涉及脂多糖诱导的肺成纤维细胞增殖

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摘要

Lipopolysaccharide (LPS)-induced pulmonary fibrosis is characterized by aberrant proliferation and activation of lung fibroblasts. Epigenetic regulation of thymocyte differentiation antigen 1 (Thy-1) is associated with lung fibroblast phenotype transformation that results in aberrant cell proliferation. However, it is not clear whether the epigenetic regulation of Thy-1 expression is required for LPS-induced lung fibroblast proliferation. To address this issue and better understand the relative underlying mechanisms, we used mouse lung fibroblasts as model to observe the changes of Thy-1 expression and histone deacetylation after LPS challenge. The results showed that cellular DNA synthesis, measured by BrdU incorporation, was impacted less in the early stage (24 hrs) after the challenge of LPS, but significantly increased at 48 or 72 hrs after the challenge of LPS. Meanwhile, Thy-1 expression, which was detected by real-time PCR and Western blot, in lung fibroblasts decreased with increased time after LPS challenge and diminished at 72 hrs. We also found that the acetylation of either histone H3 or H4 decreased in the LPS-challenged lung fibroblasts. ChIP assay revealed that the acetylation of histone H4 (Ace-H4) decreased in the Thy-1 promoter region in response to LPS. In addition, all the above changes could be attenuated by depletion of TLR4 gene. Our studies indicate that epigenetic regulation of Thy-1 gene expression by histone modification is involved in LPS-induced lung fibroblast proliferation.
机译:脂多糖(LPS)诱导的肺纤维化的特征在于肺成纤维细胞的异常增殖和激活。胸腺细胞分化抗原1(Thy-1)的表观遗传调控与导致肺细胞异常增殖的肺成纤维细胞表型转化有关。但是,尚不清楚LPS诱导的肺成纤维细胞增殖是否需要Thy-1表达的表观遗传调控。为了解决这个问题并更好地了解相关的潜在机制,我们使用小鼠肺成纤维细胞作为模型,观察了LPS攻击后Thy-1表达的变化和组蛋白脱乙酰化。结果表明,通过掺入BrdU进行测量的细胞DNA合成在LPS攻击后的早期阶段(24小时)受到的影响较小,但在LPS攻击后48或72小时受到的影响显着增加。同时,通过实时PCR和Western印迹检测到的Thy-1表达在LPS攻击后随时间增加而降低,并在72小时时降低。我们还发现在LPS攻击的肺成纤维细胞中,组蛋白H3或H4的乙酰化程度降低。 ChIP分析显示,响应LPS,Thy-1启动子区域的组蛋白H4(Ace-H4)乙酰化程度降低。此外,所有上述变化可通过TLR4基因的耗尽而减弱。我们的研究表明,通过组蛋白修饰对Thy-1基因表达进行表观遗传调控与LPS诱导的肺成纤维细胞增殖有关。

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