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High-temperature calcined fullerene nanowhiskers as well as long needle-like multi-wall carbon nanotubes have abilities to induce NLRP3-mediated IL-1β secretion

•Metal impurities in carbon nanotubes may be responsible for their toxicity.•Fullerene nanowhiskers have similar sizes and shape but no metal impurities.•Long high-temperature calcined fullerene nanowhiskers induce IL-1β secretion.•Knockdown of NLRP3 abolished the IL-1β secretion.•Needle-like shape...

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Published in:Biochemical and biophysical research communications 2014-09, Vol.452 (3), p.593-599
Main Authors: Cui, Hongyan, Wu, Weijia, Okuhira, Keiichiro, Miyazawa, Kun’ichi, Hattori, Takayuki, Sai, Kimie, Naito, Mikihiko, Suzuki, Kazuhiro, Nishimura, Tetsuji, Sakamoto, Yoshimitsu, Ogata, Akio, Maeno, Tomokazu, Inomata, Akiko, Nakae, Dai, Hirose, Akihiko, Nishimaki-Mogami, Tomoko
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Language:English
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Summary:•Metal impurities in carbon nanotubes may be responsible for their toxicity.•Fullerene nanowhiskers have similar sizes and shape but no metal impurities.•Long high-temperature calcined fullerene nanowhiskers induce IL-1β secretion.•Knockdown of NLRP3 abolished the IL-1β secretion.•Needle-like shape and size but not metal impurities were critical to NLRP3 activation. Because multi-wall carbon nanotubes (MWCNTs) have asbestos-like shape and size, concerns about their pathogenicity have been raised. Contaminated metals of MWCNTs may also be responsible for their toxicity. In this study, we employed high-temperature calcined fullerene nanowhiskers (HTCFNWs), which are needle-like nanofibers composed of amorphous carbon having similar sizes to MWCNTs but neither metal impurities nor tubular structures, and investigated their ability to induce production a major proinflammatory cytokine IL-1β via the Nod-like receptor pyrin domain containing 3 (NLRP3)-containing flammasome-mediated mechanism. When exposed to THP-1 macrophages, long-HTCFNW exhibited robust IL-1β production as long and needle-like MWCNTs did, but short-HTCFNW caused very small effect. IL-1β release induced by long-HTCFNW as well as by long, needle-like MWCNTs was abolished by a caspase-1 inhibitor or siRNA-knockdown of NLRP3, indicating that NLRP3-inflammasome-mediated IL-1β production by these carbon nanofibers. Our findings indicate that the needle-like shape and length, but neither metal impurities nor tubular structures of MWCNTs were critical to robust NLRP3 activation.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2014.08.118