U.S. Environmental Protection Agency, Office of Research and Development, National Health and Environmental Effects Research Laboratory, Toxicology Assessment Division, Research Triangle Park, NC, United States of America.
Oak Ridge Institute for Science and Education (ORISE) appointee at the National Health and Environmental Effects Research Laboratory, USEPA, RTP, NC, United States of America.
PLoS One. 2019 Jul 31;14(7):e0219078. doi: 10.1371/journal.pone.0219078. eCollection 2019.
This study compared the relative cellular uptake of 80 nm silver nanoparticles (AgNP) with four different coatings including: branched polyethyleneimine (bPEI), citrate (CIT), polyvinylpyrrolidone (PVP), and polyethylene glycol (PEG). A gold nanoparticle PVP was also compared to the silver nanoparticles. Biophysical parameters of cellular uptake and effects included flow cytometry side scatter (SSC) intensity, nuclear light scatter, cell cycle distributions, surface plasmonic resonance (SPR), fluorescence microscopy of mitochondrial gross structure, and darkfield hyperspectral imaging. The AgNP-bPEI were positively charged and entered cells at a higher rate than the negatively or neutrally charged particles. The AgNP-bPEI were toxic to the cells at lower doses than the other coatings which resulted in mitochondria being transformed from a normal string-like appearance to small round beaded structures. Hyperspectral imaging showed that AgNP-bPEI and AgNP-CIT agglomerated in the cells and on the slides, which was evident by longer spectral wavelengths of scattered light compared to AgNP-PEG and AgNP-PVP particles. In unfixed cells, AgNP-CIT and AgNP-bPEI had higher SPR than either AgNP-PEG or AgNP-PVP particles, presumably due to greater intracellular agglomeration. After 24 hr. incubation with AgNP-bPEI, there was a dose-dependent decrease in the G1 phase and an increase in the G2/M and S phases of the cell cycle suggestive of cell cycle inhibition. The nuclei of all the AgNP treated cells showed a dose-dependent increase in nanoparticles following non-ionic detergent treatment in which the nuclei retained extra-nuclear AgNP, suggesting that nanoparticles were attached to the nuclei or cytoplasm and not removed by detergent lysis. In summary, positively charged AgNP-bPEI increased particle cellular uptake. Particles agglomerated in the peri-nuclear region, increased mitochondrial toxicity, disturbed the cell cycle, and caused abnormal adherence of extranuclear material to the nucleus after detergent lysis of cells. These results illustrate the importance of nanoparticle surface coatings and charge in determining potentially toxic cellular interactions.
本研究比较了 80nm 银纳米粒子(AgNP)与四种不同涂层的相对细胞摄取率,包括:支化聚乙烯亚胺(bPEI)、柠檬酸(CIT)、聚乙烯吡咯烷酮(PVP)和聚乙二醇(PEG)。还比较了金纳米粒子 PVP 与银纳米粒子。细胞摄取的生物物理参数和影响包括流式细胞术侧散射(SSC)强度、核光散射、细胞周期分布、表面等离子体共振(SPR)、线粒体宏观结构的荧光显微镜观察以及暗场高光谱成像。AgNP-bPEI 带正电荷,进入细胞的速度比带负电荷或不带电荷的颗粒快。AgNP-bPEI 在较低剂量下对细胞有毒,比其他涂层更严重,导致线粒体从正常的线状外观转变为小的圆形珠状结构。高光谱成像显示,AgNP-bPEI 和 AgNP-CIT 在细胞内和载玻片上聚集,与 AgNP-PEG 和 AgNP-PVP 颗粒相比,散射光的光谱波长更长,这一点很明显。在未固定的细胞中,AgNP-CIT 和 AgNP-bPEI 的 SPR 高于 AgNP-PEG 或 AgNP-PVP 颗粒,推测是由于细胞内聚集更多。在用 AgNP-bPEI 孵育 24 小时后,细胞周期的 G1 期呈剂量依赖性下降,G2/M 和 S 期增加,表明细胞周期受到抑制。在用非离子型去污剂处理后,所有 AgNP 处理的细胞核中的纳米颗粒均呈剂量依赖性增加,细胞核保留了核外 AgNP,这表明纳米颗粒附着在核或细胞质上,而不是通过去污剂裂解去除。总之,带正电荷的 AgNP-bPEI 增加了颗粒的细胞摄取。颗粒在核周区域聚集,增加了线粒体毒性,扰乱了细胞周期,并在细胞用去污剂裂解后导致核外物质异常附着在核上。这些结果说明了纳米颗粒表面涂层和电荷在确定潜在毒性细胞相互作用中的重要性。