Martin Ansie, Sarkar Angshuman
a Department of Biological Sciences , CMBL, BITS Pilani K K Birla Goa Campus , Zuarinagar , India.
Nanotoxicology. 2017 Aug;11(6):713-724. doi: 10.1080/17435390.2017.1366574. Epub 2017 Aug 23.
Metal oxides (MeOx) are exponentially being used in a wide range of applications and are the largest class of commercially produced nanomaterials. This presents unprecedented human exposure. Thus, understanding nanoparticle induced cellular stress can greatly help design strategies to combat them. Scores of studies have been carried out to understand the effects of MeOx nanoparticle exposure on human alveolar cells, which are highly susceptible to aerosolized matter. There is a huge redundancy of information generated, also, a lack of a comprehensive conglomeration of this information. We have built here in a sincere summary of the cellular responses reported till date as a direct consequence of MeOx nanoparticle exposure on human alveolar (A549) cells. Detailed accounts of cellular morphology modulation, generation of reactive oxygen species (ROS) and oxidative stress, inflammation and cytokine release, genotoxic and epi-genotoxic insults, toxicological trend, nanoparticle internalization, modes of cell death, protein synthesis, and membrane damage among others are discussed. Finally, to aid predictability of the highly dynamic and multifactorial nature of this toxicity, we have hypothesized models that describe the ensuing mechanisms based on common patterns discovered throughout our literature survey.
金属氧化物(MeOx)正越来越广泛地应用于各种领域,是商业生产的纳米材料中最大的一类。这带来了前所未有的人类接触风险。因此,了解纳米颗粒诱导的细胞应激对于制定应对策略具有极大的帮助。为了了解MeOx纳米颗粒暴露对人类肺泡细胞的影响,已经开展了大量研究,因为人类肺泡细胞对气溶胶物质高度敏感。研究产生了大量冗余信息,而且缺乏对这些信息的全面整合。在此,我们真诚地总结了迄今为止报道的、作为MeOx纳米颗粒暴露对人肺泡(A549)细胞直接影响的细胞反应。文中讨论了细胞形态调节、活性氧(ROS)生成与氧化应激、炎症与细胞因子释放、基因毒性和表观遗传毒性损伤、毒理学趋势、纳米颗粒内化、细胞死亡模式、蛋白质合成以及膜损伤等方面的详细情况。最后,为了帮助预测这种毒性高度动态和多因素的性质,我们基于文献调研中发现的共同模式,提出了描述后续机制的假设模型。