Carbon black and titanium dioxide nanoparticles induce distinct molecular mechanisms of toxicity.
Carbon black and titanium dioxide nanoparticles induce distinct molecular mechanisms of toxicity.
复制标题
DOI:
10.1002/wnan.1302
复制
发表时间:
2014-11
影响因子:
8.6
通讯作者:
Baeza-Squiban, Armelle
中科院分区:
文献类型:
--
作者:
Boland, Sonja;Hussain, Salik;Baeza-Squiban, Armelle
Increasing evidence link nanomaterials with adverse biological outcomes and due to the variety of applications and potential human exposures to nanoparticles it is thus important to evaluate their toxicity for the risk assessment of workers and consumers. It is crucial to understand the underlying mechanisms of their toxicity as observation of similar effects after different nanomaterial exposures does not reflect similar intracellular processing and organelle interactions. A thorough understanding of mechanisms is not only needed for accurate prediction of potential toxicological impacts but also for the development of safer nanoapplications by modulating the physico-chemical characteristics. Furthermore biomedical applications may also take advantage of an in depth knowledge about the mode of action of nanotoxicity to design new nanoparticle-derived drugs. In the present manuscript we discuss the similarities and differences in molecular pathways of toxicity after carbon black and TiO2 nanoparticle exposures and identify the main toxicity mechanisms induced by these two nanoparticles which may also be indicative for the mode of action of other insoluble nanomaterials. We address the translocation, cell death induction, genotoxicity and inflammation induced by titanium dioxide and carbon black nanoparticles which depend on their internalisation, ROS production capacities and/or protein interactions. We summarise their distinct cellular mechanisms of toxicity and the crucial steps which may be targeted to avoid adverse effects or to induce them for nanomedical purposes. Several physico-chemical characteristics could influence these general toxicity pathways depicted here and the identification of common toxicity pathways could support the grouping of nanomaterials in terms of toxicity.
登录
查看更多内容
影响因子:
10
作者:
Hussain S;Smulders S;De Vooght V;Ectors B;Boland S;Marano F;Van Landuyt KL;Nemery B;Hoet PH;Vanoirbeek JA
通讯作者:
Vanoirbeek JA
影响因子:
8.8
作者:
Koike, Eiko;Takano, Hirohisa;Kobayashi, Takahiro
通讯作者:
Kobayashi, Takahiro
影响因子:
3.7
作者:
Ale-Agha, Niloofar;Albrecht, Catrin;Klotza, Lars-Oliver
通讯作者:
Klotza, Lars-Oliver
影响因子:
3.9
作者:
Deng, Zhou J.;Butcher, Neville J.;Minchin, Rodney F.
通讯作者:
Minchin, Rodney F.
影响因子:
18.3
作者:
Kreyling, Wolfgang G.;Semmler-Behnke, Manuela;Takenaka, Shinji;Moeller, Winfried
通讯作者:
Moeller, Winfried