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Open Access Green as soon as Postprint is submitted to ZB.
SWCNT suppress inflammatory mediator responses in human lung epithelium in vitro.
Toxicol. Appl. Pharmacol. 234, 378-390 (2009)
Single-walled carbon nanotubes have gained enormous popularity due to a variety of potential applications which will ultimately lead to increased human and environmental exposure to these nanoparticles. This study was carried out in order to evaluate the inflammatory response of immortalised and primary human lung epithelial cells (A549 and NHBE) to single-walled carbon nanotube samples (SWCNT). Special focus was placed on the mediating role of lung surfactant on particle toxicity. The toxicity of SWCNT dispersed in cell culture medium was compared to that of nanotubes dispersed in dipalmitoylphosphatidylcholine (DPPC, the main component of lung lining fluid). Exposure was carried out for 6 to 48 h with the latter time-point showing the most significant responses. Moreover, exposure was performed in the presence of the pro-inflammatory stimulus tumour necrosis factor-alpha (TNF-alpha) in order to mimic exposure of stimulated cells, as would occur during infection. Endpoints evaluated included cell viability, proliferation and the analysis of inflammatory mediators such as interleukin (IL)-8, IL-6, TNF-alpha and macrophage chemoattractant protein-1 (MCP-1). Crocidolite asbestos was included as a well characterised, toxic fibre control. The results of this study showed that HiPco SWCNT samples suppress inflammatory responses of A549 and NHBE cells. This was also true for TNF-alpha stimulated cells. The use of DPPC improved the degree of SWCNT dispersion in A549 medium and in turn, leads to increased particle toxicity, however, it was not shown to modify NHBE cell responses.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Nanoparticles; Single-walled carbon nanotubes (SWCNT); Dipalmitoylphosphatidyl-choline (DPPC); Lung surfactant; Inflammatory mediators; A549 cell-line; NHBE cell-line; Lung epithelium; diesel-exhaust particles; walled carbon nanotubes; pulmonary surfactant; alveolar macrophages; air-pollution; ii cells; asbestos; toxicity; nanoparticles; health
ISSN (print) / ISBN
0041-008X
e-ISSN
1096-0333
Quellenangaben
Volume: 234,
Issue: 3,
Pages: 378-390
Publisher
Elsevier
Non-patent literature
Publications
Reviewing status
Peer reviewed
Institute(s)
Lung Health and Immunity (LHI)