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Effects of cell culture media on the dynamic formation of protein-nanoparticle complexes and influence on the cellular response

机译:细胞培养基对蛋白质-纳米颗粒复合物动态形成的影响及其对细胞应答的影响

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The development of appropriate in vitro protocols to assess the potential toxicity of the ever expanding range of nanoparticles represents a challenging issue, because of the rapid changes of their intrinsic physicochemical properties (size, shape, reactivity, surface area, etc.) upon dispersion in biological fluids. Dynamic formation of protein coating around nanoparticles is a key molecular event, which may strongly impact the biological response in nanotoxicological tests. In this work, by using citrate-capped gold nanoparticles (AuNPs) of different sizes as a model, we show, by several spectroscopic techniques (dynamic light scattering, UV-visible, plasmon resonance light scattering), that proteins-NP interactions are differently mediated by two widely used cellular media (i.e., Dulbecco Modified Eagle's medium (DMEM) and Roswell Park Memorial Institute medium (RPMI), supplemented with fetal bovine serum). We found that, while DMEM elicits the formation of a large time-dependent protein corona, RPMI shows different dynamics with reduced protein coating. Characterization of these nanobioentities was also performed by sodium dodecyl sulfate polyacrylamide gel electrophoresis and mass spectroscopy, revealing that the average composition of protein corona does not reflect the relative abundance of serum proteins. To evaluate the biological impact of such hybrid bionanostructures, several comparative viability assays onto two cell lines (HeLa and U937) were carried out in the two media, in the presence of 15 nm AuNPs. We observed that proteins/NP complexes formed in RPMI are more abundantly internalized in cells as compared to DMEM, overall exerting higher cytotoxic effects. These results show that, beyond an in-depth NPs characterization before cellular experiments, a detailed understanding of the effects elicited by cell culture media on NPs is crucial for standardized nanotoxicology tests.
机译:由于在分散于纳米颗粒中后其内在的理化性质(尺寸,形状,反应性,表面积等)迅速变化,因此开发适当的体外方案以评估不断扩大的纳米颗粒的潜在毒性是一个具有挑战性的问题。生物液体。纳米颗粒周围蛋白质涂层的动态形成是关键的分子事件,可能会严重影响纳米毒理学测试中的生物学反应。在这项工作中,通过使用不同大小的柠檬酸封端的金纳米粒子(AuNPs)作为模型,我们通过几种光谱技术(动态光散射,紫外可见光,等离振子共振光散射)表明,蛋白质与NP的相互作用是不同的由两种广泛使用的细胞培养基(即,Dulbecco改良的Eagle培养基(DMEM)和罗斯维尔公园纪念学院培养基(RPMI),并补充了胎牛血清)介导。我们发现,尽管DMEM引发了大的时间依赖性蛋白电晕的形成,但RPMI显示出不同的动力学,且蛋白涂层减少。还通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳和质谱法对这些纳米生物实体进行了表征,发现蛋白质电晕的平均组成不能反映血清蛋白质的相对丰度。为了评估这种杂合的生物纳米结构的生物学影响,在两种介质中,存在15 nm AuNP的情况下,对两种细胞系(HeLa和U937)进行了几种比较生存力测定。我们观察到,与DMEM相比,RPMI中形成的蛋白质/ NP复合物在细胞中的内化程度更高,总体上具有更高的细胞毒性作用。这些结果表明,除了在细胞实验之前对NP进行深入表征外,对细胞培养基对NP产生的影响的详细了解对于标准化的纳米毒理学测试至关重要。

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