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NADPH Oxidase‐Dependent NLRP3 Inflammasome Activation and its Important Role in Lung Fibrosis by Multiwalled Carbon Nanotubes
Author(s) -
Sun Bingbing,
Wang Xiang,
Ji Zhaoxia,
Wang Meiying,
Liao YuPei,
Chang Chong Hyun,
Li Ruibin,
Zhang Haiyuan,
Nel André E.,
Xia Tian
Publication year - 2015
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201402859
Subject(s) - nadph oxidase , inflammasome , reactive oxygen species , respiratory burst , p22phox , pulmonary fibrosis , biophysics , materials science , chemistry , fibrosis , oxidative stress , biochemistry , biology , medicine , receptor , pathology
The purpose of this paper is to elucidate the key role of NADPH oxidase in NLRP3 inflammasome activation and generation of pulmonary fibrosis by multi‐walled carbon nanotubes (MWCNTs). Although it is known that oxidative stress plays a role in pulmonary fibrosis by single‐walled CNTs, the role of specific sources of reactive oxygen species, including NADPH oxidase, in inflammasome activation remains to be clarified. In this study, three long aspect ratio (LAR) materials (MWCNTs, single‐walled carbon nanotubes, and silver nanowires) are used to compare with spherical carbon black and silver nanoparticles for their ability to trigger oxygen burst activity and NLRP3 assembly. All LAR materials but not spherical nanoparticles induce robust NADPH oxidase activation and respiratory burst activity in THP‐1 cells, which are blunted in p22 phox ‐deficient cells. The NADPH oxidase is directly involved in lysosomal damage by LAR materials, as demonstrated by decreased cathepsin B release and IL‐1β production in p22 phox ‐deficient cells. Reduced respiratory burst activity and inflammasome activation are also observed in bone marrow‐derived macrophages from p47 phox ‐deficient mice. Moreover, p47 phox ‐deficient mice have reduced IL‐1β production and lung collagen deposition in response to MWCNTs. Lung fibrosis is also suppressed by N‐acetyl‐cysteine in wild‐type animals exposed to MWCNTs.