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金纳米粒子的尺寸依赖性毒性和对小鼠成纤维细胞的细胞相互作用机制。

Size-dependent toxicity and cell interaction mechanisms of gold nanoparticles on mouse fibroblasts.

机构信息

Nanobiosciences Unit, Joint Research Centre, Institute for Health and Consumer Protection, European Commission, Via E. Fermi 2749, 21027 Ispra, VA, Italy.

出版信息

Toxicol Lett. 2013 Mar 13;217(3):205-16. doi: 10.1016/j.toxlet.2012.11.022. Epub 2012 Dec 13.

Abstract

Gold nanoparticles (AuNPs) are currently used in several fields including biomedical applications, although no conclusive information on their cytotoxicity is available. For this reason this work has investigated the effects of AuNPs in vitro on Balb/3T3 mouse fibroblasts. Results obtained exposing cells for 72 h to AuNPs 5 and 15 nm citrate stabilized, revealed cytotoxic effects only for AuNPs 5 nm at concentration ≥ 50 μM if measured by colony forming efficiency (CFE). To understand the differences in cytotoxicity observed for the two AuNPs sizes, we investigated the uptake and the intracellular distribution of the nanoparticles. By TEM it was observed that 5 and 15 nm AuNPs are internalized by Balb/3T3 cells and located within intracellular endosomal compartments. Quantification of the uptake by ICP-MS showed that AuNPs internalization enhanced even up to 72 h. Disruption of the actin cytoskeleton was evident, with cell footprints narrow and contracted; effects more remarkable in cells exposed to 5 nm AuNP. The mechanism of NPs cell internalization was investigated using immunocytochemistry and western blot. No significant effect was observed in the expression level of caveolin, while reduction of the expression and degradation of the clathrin heavy chain was observed in cells exposed for 72 h to AuNPs.

摘要

金纳米粒子(AuNPs)目前被应用于多个领域,包括生物医学应用,尽管它们的细胞毒性尚无明确信息。出于这个原因,这项工作研究了体外暴露于柠檬酸稳定的 5nm 和 15nm AuNPs 72 小时对 Balb/3T3 小鼠成纤维细胞的影响。结果表明,只有当浓度≥50μM 时,5nm AuNPs 才会对细胞产生细胞毒性,通过集落形成效率(CFE)来衡量。为了理解两种 AuNPs 尺寸观察到的细胞毒性差异,我们研究了纳米颗粒的摄取和细胞内分布。通过 TEM 观察到,5nm 和 15nm AuNPs 被 Balb/3T3 细胞内化,并位于细胞内的内体隔室内。ICP-MS 的摄取定量表明,纳米颗粒的内化作用甚至在 72 小时后仍增强。肌动蛋白细胞骨架的破坏是明显的,细胞足迹变窄和收缩;在暴露于 5nm AuNP 的细胞中,这些影响更为显著。通过免疫细胞化学和 Western blot 研究了 NPs 细胞内化的机制。在暴露于 AuNPs 72 小时的细胞中,未观察到窖蛋白表达水平的显著影响,而网格蛋白重链的表达和降解减少。

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