MWCNTs of different physicochemical properties cause similar inflammatory responses, but differences in transcriptional and histological markers of fibrosis in mouse lungs

Multi-walled carbon nanotubes (MWCNTs) are extensively produced and used in composite materials and electronic applications, thus increasing risk of worker and consumer exposure. MWCNTs are an inhomogeneous group of nanomaterials that come in various lengths, shapes and with different metal contaminations, which makes hazard evaluation difficult. However, several studies suggest that length plays an important role in the toxicity induced by MWCNTs. How the length influences toxicity at the molecular level is yet to be characterized. Female C57BL/6 mice were exposed by single intratracheal instillation to 18, 54 or 162 µg/mouse of a short MWCNT (NRCWE-026, 847±102 nm in length) or long MWCNT (NM-401, 4048±366 nm in length). The two MWCNTs were extensively characterized. Lung tissues were harvested 24 h, 3 d and 28 d after exposure. We employed DNA microarrays, bronchoalveolar lavage fluid analysis, comet assay and dichlorodihydrofluorescein assay in order to profile the pulmonary responses. Bioinformatics tools were then applied to compare and contrast the expression profiles and to build a length dependent property-response matrix for gene-by-gene comparison. The toxicogenomic analysis of the global mRNA changes after exposure to the short, entangled NRCWE-026 or the longer, stiffer NM-401 showed high degree of similarities. The toxicity of both MWCNTs was driven by strong inflammatory and acute phase responses, which peaked at day 3 and was observed both in bronchoalveolar lavage cell influx and in gene expression profiles. The inflammatory response was sustained at post-exposure day 28. Also, at the sub-chronic level, we identified a sub-set of 14 fibrosis related genes that were uniquely differentially regulated after exposure to NM-401. Acellular ROS production occurred almost exclusively with NRCWE-026, however the longer NM-401 induced in vivo DNA strand breaks and differential regulation of genes involved in free radical scavenging more readily than NRCWE-026. Our results indicate that the global mRNA response after exposure to MWCNTs is length independent at the acute time points, but that fibrosis may be length dependent sub-chronic end point.

POULSEN Sarah Søs;  SABER Anne T;  WILLIAMS Andrew;  ANDERSEN Ole;  KØBLER Carsten;  ATLURI Rambabu;  POZZEBON Mariaelena;  MUCELLI Stefano P;  SIMION Monica;  RICKERBY David;  MORTENSEN Alicja;  JACKSON Petra;  KYJOVSKA Zdenka O.;  MØLHAVE Kristian;  JACOBSEN Nicklas R;  JENSEN Keld Astrup;  YAUK Carole L;  WALLIN Håkan;  HALAPPANAVAR Sabina;  VOGEL Ulla; 

2015-04-14

ACADEMIC PRESS INC ELSEVIER SCIENCE

JRC94090

0041-008X,   

http://www.sciencedirect.com/science/article/pii/S0041008X14004499,    https://publications.jrc.ec.europa.eu/repository/handle/JRC94090,   

10.1016/j.taap.2014.12.011,