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脑微血管内皮细胞对金纳米颗粒的反应:体外促炎介质和通透性。

Brain microvessel endothelial cells responses to gold nanoparticles: In vitro pro-inflammatory mediators and permeability.

机构信息

Neurochemistry Laboratory, Division of Neurotoxicology, National Center of Toxicological Research/FDA, Jefferson, Arkansas, USA.

出版信息

Nanotoxicology. 2011 Dec;5(4):479-92. doi: 10.3109/17435390.2010.540356. Epub 2010 Dec 22.

DOI:10.3109/17435390.2010.540356
PMID:21175299
Abstract

This report examined blood-brain barrier (BBB) related proinflammatory mediators and permeability changes in response to various sized gold nanoparticles (Au-NPs) (3, 5, 7, 10, 30 and 60 nm) in vitro using primary rat brain microvessel endothelial cells (rBMEC). The Au-NPs were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS) and laser Doppler velocimetry (LDV). The accumulation of Au-NPs was determined spectrophotometrically. The rBMEC cytotoxicity of Au-NPs was evaluated by cell proliferation assay (XTT) (concentration range 0.24-15.63 μg/cm², for 24 h). The time-dependent changes (0, 2, 4 and 8 h) of several proinflammatory mediators (IL-1β, IL-2, TNFα and PGE₂) were evaluated by ELISA. The smaller Au-NPs (3-7 nm) showed higher rBMEC accumulation compared to larger Au-NPs (10-60 nm), while only moderate decreased cell viability was observed with small Au-NPs (3 nm) at high concentrations (≥ 7.8 μg/cm²). Even though slight changes in cell viability were observed with small Au-NPs, the basal levels of the various proinflammatory mediators remained unchanged with all treatments except LPS (positive control). rBMEC morphology appeared unaffected 24 h after exposure to Au-NPs with only mild changes in fluorescein permeability indicating BBB integrity was unaltered. Together, these data suggest the responses of the cerebral microvasculature to Au-NPs have a significant relationship with the Au-NPs unique size-dependent physiochemical properties.

摘要

本报告研究了血脑屏障 (BBB) 相关促炎介质和通透性的变化,以响应各种大小的金纳米粒子 (Au-NPs) (3、5、7、10、30 和 60nm) 在体外使用原代大鼠脑微血管内皮细胞 (rBMEC)。Au-NPs 通过透射电子显微镜 (TEM)、动态光散射 (DLS) 和激光多普勒速度计 (LDV) 进行表征。Au-NPs 的积累通过分光光度法确定。通过细胞增殖测定 (XTT) (浓度范围 0.24-15.63μg/cm²,24 小时) 评估 Au-NPs 对 rBMEC 的细胞毒性。通过 ELISA 评估几种促炎介质 (IL-1β、IL-2、TNFα 和 PGE₂) 的时间依赖性变化 (0、2、4 和 8 小时)。与较大的 Au-NPs (10-60nm) 相比,较小的 Au-NPs (3-7nm) 显示出更高的 rBMEC 积累,而只有小的 Au-NPs (3nm) 在高浓度 (≥7.8μg/cm²) 时才观察到适度降低细胞活力。尽管小的 Au-NPs 观察到细胞活力的轻微变化,但除 LPS(阳性对照)外,所有处理的各种促炎介质的基础水平保持不变。暴露于 Au-NPs 24 小时后,rBMEC 形态似乎不受影响,只有荧光素通透性的轻微变化表明 BBB 完整性未改变。总之,这些数据表明,大脑微血管对 Au-NPs 的反应与 Au-NPs 独特的尺寸依赖性物理化学特性有显著关系。

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