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首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >Cytotoxicity and inflammation in human alveolar epithelial cells following exposure to occupational levels of gold and silver nanoparticles
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Cytotoxicity and inflammation in human alveolar epithelial cells following exposure to occupational levels of gold and silver nanoparticles

机译:暴露于职业水平的金和银纳米粒子后,人肺泡上皮细胞的细胞毒性和炎症

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While inhalation represents one of the most likely routes of exposure, the toxicity and response of nanoparticles at concentrations expected from such an exposure are not well understood. Here we characterized the in vitro response of human A549 adenocarcinomic alveolar epithelial cells following exposure to gold (AuNP) and silver (AgNP) nanoparticles at levels approximating an occupational exposure. Changes in neither oxidative stress nor cytotoxicity were significantly affected by exposure to AgNPs and AuNPs, regardless of NP type (Ag vs. Au), concentration, surface ligand (citrate or tannic acid), or size. An inflammatory response was, however, observed in response to 20 nm AgNPs and 20 nm AuNPs, where significant differences in the release of interleukin (IL)- 8 but not IL-6 were observed. Additional data demonstrated that increased IL-8 secretion was strongly dependent on both nanoparticle size and concentration. Overall these data suggest that, while not acutely toxic, occupational exposure to AuNPs and AgNPs may trigger a significant inflammatory response in alveolar epithelium. Moreover, the differential responses in IL-8 and IL-6 secretion suggest that NPs may induce a response pathway that is distinct from those commonly elicited by allergens and pathogens.
机译:虽然吸入代表了最可能的接触途径之一,但人们对这种接触所期望的浓度下的纳米颗粒的毒性和反应还没有很好的了解。在这里,我们表征了在暴露于金(AuNP)和银(AgNP)纳米粒子的水平接近于职业暴露后,人A549腺癌的肺泡上皮细胞的体外反应。暴露于AgNPs和AuNPs不会显着影响氧化应激和细胞毒性的变化,而与NP类型(Ag对Au),浓度,表面配体(柠檬酸或单宁酸)或大小无关。然而,观察到针对20nm AgNP和20nm AuNP的炎症反应,其中在白介素(IL)-8的释放中观察到显着差异,但在IL-6中未观察到。其他数据表明,IL-8分泌的增加强烈取决于纳米颗粒的大小和浓度。总体而言,这些数据表明,职业暴露于AuNPs和AgNPs虽无急性毒性,但可能在肺泡上皮中引发明显的炎症反应。此外,IL-8和IL-6分泌的差异反应表明,NPs可能诱导不同于通常由过敏原和病原体引起的反应的途径。

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