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Vascular effects of multiwalled carbon nanotubes in dyslipidemic ApoE-/- mice and cultured endothelial cells.
Toxicol. Sci. 138, 104-116 (2014)
Accumulating evidences indicate that pulmonary exposure to carbon nanotubes (CNTs) is associated with increased risk of lung diseases, whereas the effect on the vascular system is less studied. We investigated vascular effects of 2 types of multiwalled CNTs (MWCNTs) in apolipoprotein E-/- mice, wild-type mice, and cultured cells. The ApoE-/- mice had accelerated plaque progression in aorta after 5 intracheal instillations of MWCNT (25.6 μg/mouse weekly for 5 weeks). The exposure was associated with pulmonary inflammation, lipid peroxidation, and increased expression of inflammatory, oxidative stress, DNA repair, and vascular activation response genes. The level of oxidatively damaged DNA in lung tissue was unaltered, probably due to increased DNA repair capacities. Despite upregulation of inflammatory genes in the liver, effects on systemic cytokines and lipid peroxidation were minimal. The exposure to MWCNTs in cultured human endothelial cells increased the expression of cell adhesion molecules (ICAM1 and VCAM1). In cocultures, there was increased adhesion of monocytes to endothelial cells after exposure to MWCNT. The exposure to both types of MWCNT was also associated with increased lipid accumulation in monocytic-derived foam cells, which was dependent on concomitant oxidative stress because the antioxidant N-acetylcysteine inhibited the lipid accumulation. Collectively, our results indicate that exposure to MWCNT is associated with accelerated progression of atherosclerosis, which could be related to both increased adherence of monocytes onto the endothelium and oxidative stress-mediated transformation of monocytes to foam cells.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
8-isoprostanes ; Atherosclerosis ; Comet Assay ; Lipid Accumulation. ; Multiwalled Carbon Nanotubes ; Oxidative Stress; Oxidatively Damaged Dna; Adhesion Molecule Expression; Diesel Exhaust Particles; Lung Epithelial-cells; Pulmonary Exposure; Inhalation Exposure; Particulate Matter; Apoe(-/-) Mice; Mouse Lung; Wood Smoke
ISSN (print) / ISBN
1096-6080
e-ISSN
1096-0929
Journal
Toxicological Sciences
Quellenangaben
Volume: 138,
Issue: 1,
Pages: 104-116
Publisher
Oxford University Press
Publishing Place
Oxford
Non-patent literature
Publications
Reviewing status
Peer reviewed
Institute(s)
Lung Health and Immunity (LHI)