银纳米粒子诱导黑腹果蝇热休克蛋白 70、氧化应激和细胞凋亡。
Silver nanoparticles induced heat shock protein 70, oxidative stress and apoptosis in Drosophila melanogaster.
机构信息
Department of Biology, Center for Tissue Regeneration and Engineering, University of Dayton, Dayton, OH 45469, USA.
出版信息
Toxicol Appl Pharmacol. 2010 Feb 1;242(3):263-9. doi: 10.1016/j.taap.2009.10.016. Epub 2009 Oct 27.
Due to the intensive commercial application of silver nanoparticles (Ag NPs), risk assessment of this nanoparticle is of great importance. Our previous in vitro study demonstrated that Ag NPs caused DNA damage and apoptosis in mouse embryonic stem cells and fibroblasts. However, toxicity of Ag NPs in vivo is largely lacking. This study was undertaken to examine the toxic effects of well-characterized polysaccharide coated 10 nm Ag NPs on heat shock stress, oxidative stress, DNA damage and apoptosis in Drosophila melanogaster. Third instar larvae of D. melanogaster were fed a diet of standard cornmeal media mixed with Ag NPs at the concentrations of 50 and 100 microg/ml for 24 and 48 h. Ag NPs up-regulated the expression of heat shock protein 70 and induced oxidative stress in D. melanogaster. Malondialdehyde level, an end product of lipid peroxidation was significantly higher while antioxidant glutathione content was significantly lower in Ag NPs exposed organisms. Activities of antioxidant enzyme superoxide dismutase and catalase were also significantly higher in the organisms exposed to Ag NPs. Furthermore, Ag NPs up-regulated the cell cycle checkpoint p53 and cell signaling protein p38 that are involved in the DNA damage repair pathway. Moreover, activities of caspase-3 and caspase-9, markers of apoptosis were significantly higher in Ag NPs exposed organisms. The results indicate that Ag NPs in D. melanogaster induce heat shock stress, oxidative stress, DNA damage and apoptosis. This study suggests that the organism is stressed and thus warrants more careful assessment of Ag NPs using in vivo models to determine if chronic exposure presents developmental and reproductive toxicity.
由于银纳米粒子(Ag NPs)的商业应用十分密集,因此对这种纳米粒子进行风险评估非常重要。我们之前的体外研究表明,Ag NPs 会导致小鼠胚胎干细胞和成纤维细胞的 DNA 损伤和凋亡。然而,Ag NPs 在体内的毒性在很大程度上还缺乏研究。本研究旨在探讨具有良好特性的多糖包裹的 10nm Ag NPs 对热休克应激、氧化应激、DNA 损伤和凋亡的影响。使用含有 50 和 100μg/ml Ag NPs 的标准玉米粉培养基喂养黑腹果蝇的三龄幼虫 24 和 48 小时。Ag NPs 上调了热休克蛋白 70 的表达,并诱导了 D. melanogaster 中的氧化应激。Ag NPs 暴露的生物体中丙二醛(脂质过氧化的终产物)水平显著升高,而抗氧化剂谷胱甘肽含量显著降低。暴露于 Ag NPs 的生物体中的抗氧化酶超氧化物歧化酶和过氧化氢酶的活性也显著升高。此外,Ag NPs 上调了参与 DNA 损伤修复途径的细胞周期检查点蛋白 p53 和细胞信号蛋白 p38。此外,Ag NPs 暴露的生物体中 caspase-3 和 caspase-9 的活性显著升高,这两种酶是细胞凋亡的标志物。结果表明,Ag NPs 会在 D. melanogaster 中引起热休克应激、氧化应激、DNA 损伤和凋亡。本研究表明,生物体受到了应激,因此需要使用体内模型更仔细地评估 Ag NPs,以确定慢性暴露是否会带来发育和生殖毒性。