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Pro-Inflammatory versus Immunomodulatory Effects of Silver Nanoparticles in the Lung: The Critical Role of Dose Size and Surface Modification

机译:银纳米颗粒在肺中的促炎与免疫调节作用:剂量大小和表面修饰的关键作用

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摘要

The growing use of silver nanoparticles (Ag-NPs) in consumer products raises concerns about their toxicological potential. The purpose of the study was to investigate the size- and coating-dependent pulmonary toxicity of Ag-NPs in vitro and in vivo, using an ovalbumin (OVA)-mouse allergy model. Supernatants from (5.6–45 µg/mL) Ag50-PVP, Ag200-PVP or Ag50-citrate-treated NR8383 alveolar macrophages were tested for lactate dehydrogenase and glucuronidase activity, tumor necrosis factor (TNF)-α release and reactive oxygen species (ROS) production. For the in vivo study, NPs were intratracheally instilled in non-sensitized (NS) and OVA-sensitized (S) mice (1–50 µg/mouse) prior to OVA-challenge and bronchoalveolar lavage fluid (BALF) inflammatory infiltrate was evaluated five days after challenge. In vitro results showed a dose-dependent cytotoxicity of Ag-NPs, which was highest for Ag50-polyvinilpyrrolidone (PVP), followed by Ag50-citrate, and lowest for Ag200-PVP. In vivo 10–50 µg Ag50-PVP triggered a dose-dependent pulmonary inflammatory milieu in NS and S mice, which was significantly higher in S mice and was dampened upon instillation of Ag200-PVP. Surprisingly, instillation of 1 µg Ag50-PVP significantly reduced OVA-induced inflammatory infiltrate in S mice and had no adverse effect in NS mice. Ag50-citrate showed similar beneficial effects at low concentrations and attenuated pro-inflammatory effects at high concentrations. The lung microbiome was altered by NPs instillation dependent on coating and/or mouse batch, showing the most pronounced effects upon instillation of 50 µg Ag50-citrate, which caused an increased abundance of operational taxonomic units assigned to Actinobacteria, Bacteroidetes, Firmicutes and Proteobacteria. However, no correlation with the biphasic effect of low and high Ag-NPs dose was found. Altogether, both in vitro and in vivo data on the pulmonary effects of Ag-NPs suggest the critical role of the size, dose and surface functionalization of Ag-NPs, especially in susceptible allergic individuals. From the perspective of occupational health, care should be taken by the production of Ag-NPs-containing consumer products.
机译:银纳米颗粒(Ag-NPs)在消费产品中的使用越来越多,引起了人们对其毒理学潜力的担忧。本研究的目的是使用卵清蛋白(OVA)-小鼠过敏模型研究Ag-NP在体外和体内的大小和涂层依赖性肺毒性。测试了来自(5.6–45 µg / mL)Ag50-PVP,Ag200-PVP或Ag50-柠檬酸盐处理的NR8383肺泡巨噬细胞的上清液的乳酸脱氢酶和葡糖醛酸糖苷酶活性,肿瘤坏死因子(TNF)-α释放和活性氧(ROS) ) 生产。对于体内研究,将NPs气管内滴入非致敏(NS)和OVA致敏(S)小鼠(1–50 µg /小鼠),然后再进行OVA攻击,并评估支气管肺泡灌洗液(BALF)的炎症浸润率5挑战后的几天。体外结果显示,Ag-NPs的剂量依赖性细胞毒性对Ag50-聚乙烯吡咯烷酮(PVP)最高,其次为柠檬酸Ag50,对Ag200-PVP最低。体内10–50 µg Ag50-PVP在NS和S小鼠中引起剂量依赖性的肺炎性环境,在S小鼠中明显更高,并在滴注Ag200-PVP后被抑制。出人意料的是,滴入1 µg Ag50-PVP可以显着降低S小鼠中OVA诱导的炎症浸润,而对NS小鼠则没有不利影响。柠檬酸银50在低浓度下显示出相似的有益作用,而在高浓度下则减弱了促炎作用。取决于包被和/或小鼠批次,NPs的滴注改变了肺微生物组,在滴注50 µg柠檬酸Ag50时显示出最明显的效果,这导致分配给放线菌,拟杆菌,硬毛和变形杆菌的操作分类单元数量增加。但是,没有发现与低和高剂量的Ag-NPs的双相效应相关。总的来说,关于Ag-NPs的肺部作用的体外和体内数据表明,Ag-NPs的大小,剂量和表面功能化的关键作用,特别是在易感性过敏个体中。从职业健康的角度来看,应注意生产含Ag-NPs的消费产品。

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