Simón-Vázquez Rosana, Lozano-Fernández Tamara, Dávila-Grana Angela, González-Fernández África
Immunology, Biomedical Research Center (CINBIO) & Institute of Biomedical Research of Orense, Pontevedra and Vigo (IBI), University of Vigo, Campus Lagoas Marcosende, Vigo, Pontevedra, 36310 Spain.
Future Sci OA. 2016 Apr 15;2(2):FSO118. doi: 10.4155/fso.16.2. eCollection 2016 Jun.
Nanoparticles (Nps) can induce toxicity in the lung by accidental or intentional exposure. The main objective of the study reported here was to characterize the effect that four metal oxide Nps (CeO, TiO, AlO and ZnO) had at the cellular level on a human lung epithelial cell line. This goal was achieved by studying the capacity of the Nps to activate the main mitogen-activated protein kinases (MAPKs) and the nuclear factor NFκB. Only ZnO Nps were able to activate all of the MAPKs and the release of Zn ions was the main cause of activation. ZnO and AlO Nps activated the NFκB pathway and induced the release of inflammatory cytokines. CeO and TiO Nps were found to have safer profiles. The graphical abstract was obtained using Servier Medical Art.
纳米颗粒(Nps)可通过意外或故意接触在肺部诱发毒性。本文报道的研究的主要目的是表征四种金属氧化物纳米颗粒(CeO、TiO、Al2O3和ZnO)在细胞水平上对人肺上皮细胞系的影响。通过研究纳米颗粒激活主要丝裂原活化蛋白激酶(MAPKs)和核因子NFκB的能力实现了这一目标。只有ZnO纳米颗粒能够激活所有的MAPKs,锌离子的释放是激活的主要原因。ZnO和Al2O3纳米颗粒激活了NFκB通路并诱导了炎性细胞因子的释放。发现CeO和TiO纳米颗粒具有更安全的特性。图形摘要使用赛维图像(Servier Medical Art)制作。