Journal
TOXICOLOGY AND APPLIED PHARMACOLOGY
Volume 249, Issue 1, Pages 8-15Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.taap.2010.08.019
Keywords
carbon nanotube; cytotoxicity; epithelial cell; cellular uptake measurement; mRNA; phosphorylation
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Carbon nanotubes (CNT) are cytotoxic to several cell types. However, the mechanism of CNT toxicity has not been fully studied, and dosimetric analyses of CNT in the cell culture system are lacking. Here, we describe a novel, high throughput method to measure cellular uptake of CNT using turbimetry. BEAS-2B, a human bronchial epithelial cell line, was used to investigate cellular uptake, cytotoxicity, and inflammatory effects of multi-walled CNT (MWCNT). The cytotoxicity of MWCNT was higher than that of crocidolite asbestos in BEAS-2B cells. The IC50 of MWCNT was 12 mu g/ml, whereas that of asbestos (crocidolite) was 678 mu g/ml. Over the course of 5 to 8 h, BEAS-2B cells took up 17-18% of the MWCNT when they were added to the culture medium at a concentration of 10 mu g/ml. BEAS-2B cells were exposed to 2, 5, or 10 mu g/ml of MWCNT, and total RNA was extracted for cytokine cDNA primer array assays. The culture supernatant was collected for cytokine antibody array assays. Cytokines IL-6 and IL-8 increased in a dose dependent manner at both the mRNA and protein levels. Migration inhibitory factor (MIF) also increased in the culture supernatant in response to MWCNT. A phosphokinase array study using lysates from BEAS-2B cells exposed to MWCNT indicated that phosphorylation of p38, ERK1, and HSP27 increased significantly in response to MWCNT. Results from a reporter gene assays using the NF-kappa B or AP-1 promoter linked to the luciferase gene in transiently transfected CHO-KI cells revealed that NF-kappa B was activated following MWCNT exposure, while AP-1 was not changed. Collectively, MWCNT activated NF-kappa B, enhanced phosphorylation of MAP kinase pathway components, and increased production of proinflammatory cytokines in human bronchial epithelial cells. (C) 2010 Elsevier Inc. All rights reserved.
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