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首页> 外文期刊>Biomaterials >The induction of epigenetic regulation of PROS1 gene in lung fibroblasts by gold nanoparticles and implications for potential lung injury.
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The induction of epigenetic regulation of PROS1 gene in lung fibroblasts by gold nanoparticles and implications for potential lung injury.

机译:金纳米颗粒诱导肺成纤维细胞中PROS1基因的表观遗传调控及其对潜在肺损伤的影响。

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摘要

Advances in nanotechnology have given rise to the rapid development of novel applications in biomedicine. However, our understanding in the risks and health safety of nanomaterials is still not complete and various investigations are ongoing. Here, we show that gold nanoparticles (AuNPs) significantly altered the expression of 19 genes in human fetal lung fibroblasts (using the Affymetrix Human Gene 1.0 ST Array). Among the differentially expressed genes, up-regulation of microRNA-155 (miR-155) was observed concomitant with down-regulation of the PROS1 gene. Silencing of miR-155 established PROS1 as its possible target gene. DNA methylation profiling analysis of the PROS1 gene revealed no changes in the methylation status of this gene in AuNP-treated fibroblasts. At the ultrastructural level, chromatin condensation and reorganization was observed in the nucleus of fibroblasts exposed to AuNPs. The findings provide further insights into the molecular mechanisms underlying toxicity of AuNPs and their impact on epigenetic processes.
机译:纳米技术的进步引起了生物医学新应用的迅速发展。但是,我们对纳米材料的风险和健康安全性的理解仍不完全,并且各种研究仍在进行中。在这里,我们显示金纳米颗粒(AuNPs)显着改变了人胎肺成纤维细胞中19个基因的表达(使用Affymetrix Human Gene 1.0 ST Array)。在差异表达的基因中,观察到microRNA-155(miR-155)的上调与PROS1基因的下调同时发生。 miR-155的沉默确立了PROS1作为其可能的靶基因。 DNA甲基化分析的PROS1基因揭示了在AuNP处理的成纤维细胞中,该基因的甲基化状态没有变化。在超微结构水平上,在暴露于AuNPs的成纤维细胞核中观察到染色质浓缩和重组。该发现提供了对AuNPs毒性基础的分子机制及其对表观遗传过程的影响的进一步见解。

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