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暴露于金属纳米颗粒后Gadd45α的上调:缺氧诱导因子1α的作用

Up-regulation of Gadd45α after exposure to metal nanoparticles: the role of hypoxia inducible factor 1α.

作者信息

Feng Lingfang, Zhang Yue, Jiang Mizu, Mo Yiqun, Wan Rong, Jia Zhenyu, Tollerud David J, Zhang Xing, Zhang Qunwei

机构信息

Institute of Occupational Diseases, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, People's Republic of China; Department of Environmental and Occupational Health Sciences, School of Public Health and Information Sciences, University of Louisville, Louisville, Kentucky, USA.

出版信息

Environ Toxicol. 2015 Apr;30(4):490-9. doi: 10.1002/tox.21926. Epub 2013 Nov 26.

Abstract

The increased development and use of nanoparticles in various fields may lead to increased exposure, directly affecting human health. Our current knowledge of the health effects of metal nanoparticles such as cobalt and titanium dioxide (Nano-Co and Nano-TiO2 ) is limited but suggests that some metal nanoparticles may cause genotoxic effects including cell cycle arrest, DNA damage, and apoptosis. The growth arrest and DNA damage-inducible 45α protein (Gadd45α) has been characterized as one of the key players in the cellular responses to a variety of DNA damaging agents. The aim of this study was to investigate the alteration of Gadd45α expression in mouse embryo fibroblasts (PW) exposed to metal nanoparticles and the possible mechanisms. Non-toxic doses of Nano-Co and Nano-TiO2 were selected to treat cells. Our results showed that Nano-Co caused a dose- and time-dependent increase in Gadd45α expression, but Nano-TiO2 did not. To investigate the potential pathways involved in Nano-Co-induced Gadd45α up-regulation, we measured the expression of hypoxia inducible factor 1α (HIF-1α) in PW cells exposed to Nano-Co and Nano-TiO2 . Our results showed that exposure to Nano-Co caused HIF-1α accumulation in the nucleus. In addition, hypoxia inducible factor 1α knock-out cells [HIF-1α (-/-)] and its wild-type cells [HIF-1α (+/+)] were used. Our results demonstrated that Nano-Co caused a dose- and time-dependent increase in Gadd45α expression in wild-type HIF-1α (+/+) cells, but only a slight increase in HIF-1α (-/-) cells. Pre-treatment of PW cells with heat shock protein 90 inhibitor, 17-(Allylamino)-17-demethoxygeldanamycin (17-AAG), prior to exposure to Nano-Co significantly abolished Nano-Co-induced Gadd45α expression. These results suggest that HIF-1α accumulation may be partially involved in the increased Gadd45α expression in cells exposed to Nano-Co. These findings may have important implications for understanding the potential health effects of metal nanoparticle exposure.

摘要

纳米颗粒在各个领域的开发和使用日益增加,这可能导致人类接触量增加,从而直接影响人类健康。我们目前对钴和二氧化钛等金属纳米颗粒(纳米钴和纳米二氧化钛)对健康影响的了解有限,但表明一些金属纳米颗粒可能会导致遗传毒性效应,包括细胞周期停滞、DNA损伤和细胞凋亡。生长停滞和DNA损伤诱导蛋白45α(Gadd45α)已被确定为细胞对多种DNA损伤剂反应的关键参与者之一。本研究的目的是调查暴露于金属纳米颗粒的小鼠胚胎成纤维细胞(PW)中Gadd45α表达的变化及其可能机制。选择无毒剂量的纳米钴和纳米二氧化钛处理细胞。我们的结果表明,纳米钴导致Gadd45α表达呈剂量和时间依赖性增加,但纳米二氧化钛没有。为了研究纳米钴诱导Gadd45α上调所涉及的潜在途径,我们测量了暴露于纳米钴和纳米二氧化钛的PW细胞中缺氧诱导因子1α(HIF-1α)的表达。我们的结果表明,暴露于纳米钴会导致HIF-1α在细胞核中积累。此外,使用了缺氧诱导因子1α基因敲除细胞[HIF-1α(-/-)]及其野生型细胞[HIF-1α(+/+)]。我们的结果表明,纳米钴导致野生型HIF-1α(+/+)细胞中Gadd45α表达呈剂量和时间依赖性增加,但在HIF-1α(-/-)细胞中仅略有增加。在暴露于纳米钴之前,用热休克蛋白90抑制剂17-(烯丙基氨基)-17-去甲氧基格尔德霉素(17-AAG)预处理PW细胞,可显著消除纳米钴诱导的Gadd45α表达。这些结果表明,HIF-1α积累可能部分参与了暴露于纳米钴的细胞中Gadd45α表达的增加。这些发现可能对理解金属纳米颗粒暴露的潜在健康影响具有重要意义。

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