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Uptake efficiency of surface modified gold nanoparticles does not correlate with functional changes and cytokine secretion in human dendritic cells in vitro

机译:表面修饰金纳米粒子的吸收效率与体外人树突状细胞的功能变化和细胞因子分泌无关

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摘要

Engineering nanoparticles (NPs) for immune modulation require a thorough understanding of their interaction(s) with cells. Gold NPs (AuNPs) were coated with polyethylene glycol (PEG), polyvinyl alcohol (PVA) or a mixture of both with either positive or negative surface charge to investigate uptake and cell response in monocyte-derived dendritic cells (MDDCs). Inductively coupled plasma optical emission spectrometry and transmission electron microscopy were used to confirm the presence of Au inside MDDCs. Cell viability, (pro-)inflammatory responses, MDDC phenotype, activation markers, antigen uptake and processing were analyzed. Cell death was only observed for PVA-NH2 AuNPs at the highest concentration. MDDCs internalize AuNPs, however, surface modification influenced uptake. Though limited uptake was observed for PEG-COOH AuNPs, a significant tumor necrosis factor-alpha release was induced. In contrast, (PEG + PVA)-NH2 and PVA-NH2 AuNPs were internalized to a higher extent and caused interleukin-1beta secretion. None of the AuNPs caused changes in MDDC phenotype, activation or immunological properties.
机译:用于免疫调节的工程纳米颗粒(NPs)需要全面了解其与细胞的相互作用。将金纳米颗粒(AuNP)涂以聚乙二醇(PEG),聚乙烯醇(PVA)或两者带有正负表面电荷的混合物,以研究单核细胞衍生树突状细胞(MDDC)的摄取和细胞反应。电感耦合等离子体发射光谱法和透射电子显微镜用于确认MDDC内部是否存在Au。分析细胞活力,(促)炎症反应,MDDC表型,激活标记,抗原摄取和加工。仅在最高浓度的PVA-NH2 AuNPs中观察到细胞死亡。 MDDC使AuNPs内在化,但是,表面改性影响了其吸收。尽管观察到PEG-COOH AuNPs的摄取有限,但是诱导了显着的肿瘤坏死因子-α释放。相反,(PEG + PVA)-NH2和PVA-NH2 AuNPs内在化程度更高,并导致白介素-1β分泌。没有一个AuNPs引起MDDC表型,激活或免疫学性质的改变。

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