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Multiwalled carbon nanotubes induce a fibrogenic response by stimulating reactive oxygen species production, activating NF-kB signaling, and promoting fibroblast-to-myofibroblast transformation.

Authors
He-X; Young-S-H; Schwegler-Berry-DE; Chisholm-WP; Fernback-JE; Ma-Q
Source
Chem Res Toxicol 2011 Dec; 24(12):2237-2248
NIOSHTIC No.
20040058
Abstract
Carbon nanotubes (CNTs) are novel materials with unique electronic and mechanical properties. The extremely small size, fiberlike shape, large surface area, and unique surface chemistry render their distinctive chemical and physical characteristics and raise potential hazards to humans. Several reports have shown that pulmonary exposure to CNTs caused inflammation and lung fibrosis in rodents. The molecular mechanisms that govern CNT lung toxicity remain largely unaddressed. Here, we report that multiwalled carbon nanotubes (MWCNTs) have potent, dose-dependent toxicity on cultured human lung cells (BEAS-2B, A549, and WI38-VA13). Mechanistic analyses were carried out at subtoxic doses (=20 g/mL, = 24 h). MWCNTs induced substantial ROS production and mitochondrial damage, implicating oxidative stress in cellular damage by MWCNT. MWCNTs activated the NF-kB signaling pathway in macrophages (RAW264.7) to increase the secretion of a panel of cytokines and chemokines (TNFa, IL-1, IL-6, IL-10, and MCP1) that promote inflammation. Activation of NF-kB involved rapid degradation of IkBa, nuclear accumulation of NF-kBp65, binding of NF-kB to specific DNA-binding sequences, and transactivation of target gene promoters. Finally, MWCNTs induced the production of profibrogenic growth factors TGF1 and PDGF from macrophages that function as paracrine signals to promote the transformation of lung fibroblasts (WI38-VA13) into myofibroblasts, a key step in the development of fibrosis. Our results revealed that MWCNTs elicit multiple and intertwining signaling events involving oxidative damage, inflammatory cytokine production, and myofibroblast transformation, which potentially underlie the toxicity and fibrosis in human lungs by MWCNTs.
Keywords
Nanotechnology; Fiber-deposition; Dose-response; Hazardous-materials; Toxic-dose; Toxic-effects; Toxic-materials; Respiratory-system-disorders; Pulmonary-system-disorders; Pulmonary-system; Lung; Lung-disorders; Lung-cells; Cell-function; Cell-damage; Oxidative-processes; Cytotoxic-effects; Lung-irritants; Immune-reaction; Genes; Genotoxic-effects; DNA-damage; Lung-fibrosis
Contact
Xiaoqing He, Receptor Biology Laboratory, Toxicology and Molecular Biology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, 1095 Willowdale Road, Morgantown, WV 26505, USA
CODEN
CRTOEC
CAS No.
7440-44-0
Publication Date
20111219
Document Type
Journal Article
Email Address
qam1@cdc.gov
Fiscal Year
2012
NTIS Accession No.
NTIS Price
Identifying No.
B12212011
Issue of Publication
12
ISSN
0893-228X
NIOSH Division
HELD; DART
Priority Area
Manufacturing
Source Name
Chemical Research in Toxicology
State
WV; OH
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