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TiO(2) 纳米粒子诱导人肝细胞氧化 DNA 损伤和凋亡。

TiO(2) nanoparticles induce oxidative DNA damage and apoptosis in human liver cells.

机构信息

CSIR-Indian Institute of Toxicology Research, Nanomaterial Toxicology Group, Lucknow-226001, Uttar Pradesh, India.

出版信息

Nanotoxicology. 2013 Feb;7(1):48-60. doi: 10.3109/17435390.2011.629747. Epub 2011 Nov 2.

DOI:10.3109/17435390.2011.629747
PMID:22047016
Abstract

Titanium dioxide nanoparticles (TiO(2) NPs), widely used in consumer products, paints, pharmaceutical preparations and so on, have been shown to induce cytotoxicity, genotoxicity and carcinogenic responses in vitro and in vivo. The present study revealed that TiO(2) NPs induce significant (p < 0.05) oxidative DNA damage by the Fpg-Comet assay even at 1 µg/ml concentration. A corresponding increase in the micronucleus frequency was also observed. This could be attributed to the reduced glutathione levels with concomitant increase in lipid peroxidation and reactive oxygen species generation. Furthermore, immunoblot analysis revealed an increased expression of p53, BAX, Cyto-c, Apaf-1, caspase-9 and caspase-3 and decreased the level of Bcl-2 thereby indicating that apoptosis induced by TiO(2) NPs occurs via the caspase-dependent pathway. This study systematically shows that TiO(2) NPs induce DNA damage and cause apoptosis in HepG2 cells even at very low concentrations. Hence the use of such nanoparticles should be carefully monitored.

摘要

二氧化钛纳米粒子(TiO2 NPs)广泛应用于消费品、涂料、药物制剂等领域,已被证明在体外和体内具有细胞毒性、遗传毒性和致癌作用。本研究表明,TiO2 NPs 通过 Fpg-Comet 测定法诱导明显的(p < 0.05)氧化 DNA 损伤,即使在 1 µg/ml 浓度下也是如此。还观察到微核频率的相应增加。这可能归因于谷胱甘肽水平降低,同时脂质过氧化和活性氧物质生成增加。此外,免疫印迹分析显示 p53、BAX、Cyto-c、Apaf-1、caspase-9 和 caspase-3 的表达增加,Bcl-2 水平降低,表明 TiO2 NPs 诱导的细胞凋亡是通过 caspase 依赖性途径发生的。本研究系统地表明,TiO2 NPs 即使在非常低的浓度下也会引起 HepG2 细胞的 DNA 损伤并导致细胞凋亡。因此,此类纳米粒子的使用应谨慎监测。

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