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Importance of agglomeration state and exposure conditions for uptake and pro-inflammatory responses to amorphous silica nanoparticles in bronchial epithelial cells

TitoloImportance of agglomeration state and exposure conditions for uptake and pro-inflammatory responses to amorphous silica nanoparticles in bronchial epithelial cells
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2012
AutoriGualtieri, Maurizio, Skuland T., Iversen T.-G., Låg M., Schwarze P., Bilaničová D., Pojana G., and Refsnes M.
RivistaNanotoxicology
Volume6
Paginazione700-712
Parole chiaveAnalysis of Variance, Animals, article, bovine, bronchus mucosa, Cattle, cell culture, Cell Line, Cell Survival, Confocal, controlled study, Culture media, culture medium, cytokine production, cytokine response, Cytokines, Cytotoxicity, enzyme linked immunosorbent assay, Epithelial Cells, human, human cell, Humans, inflammation, interleukin 6, interleukin 8, messenger RNA, Microscopy, Nanoparticles, Nanotoxicology, particle size, priority journal, real time polymerase chain reaction, rhodamine, Rhodamines, Serum Albumin, Silicon Dioxide, Transformed, Water
Abstract

Amorphous silica nanoparticles (SiNPs, 30 and 50 nm) and rhodamine-coated SiNPs (50 nm) were examined for their ability to induce pro-inflammatory responses and cytotoxicity in BEAS-2B cells under different experimental conditions. The SiNPs formed micrometre-sized agglomerates in the absence of bovine serum albumin (BSA) in the culture medium, whereas with BSA (0.1%) they were much less agglomerated. All the SiNPs induced IL-6 and IL-8 responses, as measured by ELISA and real-time PCR. The responses were more marked without BSA and higher for the rhodamine SiNPs than the plain ones. Rhodamine SiNPs were not taken up by cells during a 3-h exposure, even though cytokine mRNAs were up-regulated. In conclusion, agglomerated SiNPs induced more potent cytokine responses than the non-agglomerated ones; either due to the agglomeration state per se or more conceivably to a change in surface reactivity against cellular targets due to BSA. Furthermore, cytokine expression was up-regulated independently of SiNP uptake. © 2012 Informa UK, Ltd.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84867500977&doi=10.3109%2f17435390.2011.604441&partnerID=40&md5=71b72e050e2a396ea337ee78f07edd1a
DOI10.3109/17435390.2011.604441
Citation KeyGualtieri2012700