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首页> 外文期刊>Biointerphases >Deciphering an Underlying Mechanism of Differential Cellular Effects of Nanoparticles: An Example of Bach-1 Dependent Induction of HO-1 Expression by Gold Nanorod
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Deciphering an Underlying Mechanism of Differential Cellular Effects of Nanoparticles: An Example of Bach-1 Dependent Induction of HO-1 Expression by Gold Nanorod

机译:破译纳米粒子的细胞差异作用的潜在机制:金纳米棒的Bach-1依赖诱导HO-1表达的一个例子。

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Gold nanoparticles are extensively investigated for their potential biomedical applications. Therefore, it is pertinent to thoroughly evaluate their biological effects at different levels and their underlying molecular mechanism. Frequently, there are discrepancies about the biological effects of various gold nanoparticles among the reports dealing with different models. Most of the studies focused on the different biological effects of various nano-properties of the nanomaterials. We hypothesize that the biological models with different metabolic processes would be taken into account to explain the observed discrepancies of biological effects of nanomaterials. Herein, by using mouse embryo fibroblast cell line (MEF-1) and human embryonal lung fibroblast cell line (MRC-5) as in vitro models, we studied the cellular effects of gold nanorods (AuNRs) coated with poly (diallyldimethyl ammonium chloride) (PDDAC), polyethylene glycol and polystyrene sulfonae (PSS). We found that all three AuNRs had no effects on cellular viability at the concentration of 1?nM; however, AuNRs that coated with PDDAC and PSS induced significant up-regulation of heme oxygenase-1 (HO-1) which was believed to be involved in cellular defense activities in MEF-1 but not in MRC-5 cells. Further study showed that the low fundamental expression of transcription factor Bach-1, the major regulator of HO-1 expression, in MEF-1 was responsible for the up-regulation of HO-1 induced by the AuNRs. Our results indicate that although AuNRs we used are non-cytotoxic, they cell-specifically induce change of gene expression, such as HO-1. Our current study provides a good example to explain the molecular mechanisms of differential biological effects of nanomaterials in different cellular models. This finding raises a concern on evaluation of cellular effects of nanoparticles where the cell models should be critically considered.
机译:金纳米颗粒因其潜在的生物医学应用而被广泛研究。因此,有必要彻底评估它们在不同水平上的生物学作用及其潜在的分子机制。通常,在涉及不同模型的报告中,关于各种金纳米颗粒的生物效应存在差异。大多数研究集中在纳米材料的各种纳米特性的不同生物学效应上。我们假设将考虑具有不同代谢过程的生物学模型来解释观察到的纳米材料生物学效应的差异。在这里,通过使用小鼠胚胎成纤维细胞系(MEF-1)和人胚肺成纤维细胞系(MRC-5)作为体外模型,我们研究了包覆有聚二烯丙基二甲基氯化铵的金纳米棒(AuNRs)的细胞效应。 (PDDAC),聚乙二醇和聚苯乙烯砜(PSS)。我们发现,在1?nM的浓度下,所有三种AuNRs均对细胞生存力没有影响。但是,用PDDAC和PSS包被的AuNRs诱导了血红素加氧酶-1(HO-1)的显着上调,据信这与MEF-1而非MRC-5细胞的细胞防御活性有关。进一步的研究表明,MEF-1中HO-1表达的主要调节因子转录因子Bach-1的低基础表达是AuNRs诱导HO-1上调的原因。我们的结果表明,尽管我们使用的AuNRs无细胞毒性,但它们能特异性地诱导基因表达的变化,例如HO-1。我们当前的研究提供了一个很好的例子来解释纳米材料在不同细胞模型中差异生物学效应的分子机制。这一发现引起了对纳米颗粒的细胞作用评估的关注,其中应严格考虑细胞模型。

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