Abstract |
Single walled carbon nanotubes (SWCNTs) have been shown to be highly effective against a wide range of bacteria. Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) infection is a well-known mediator to prolong hospitalization and initiate chronic inflammation, yet the biological effects of SWCNTs on the pathogen-infected enterocytes remain unclear. Herein, it is shown that the low-dose SWCNT treatment attenuates the human enterocyte-like Caco-2 cells from the damage of E. coli and S. aureus infection by suppressing NLRP3 inflammasome activation. The relatively low-dose (1 and 10 μg mL(-1) ) SWCNT treatments reduce the adhesion and invasion of E. coli and S. aureus to Caco-2 cells, increase the cell viability and proliferation, reduce the tight junction permeability, and restitute the integrity of cell surface microvilli structure, meanwhile has low cytotoxicity to the host cells. The low-dose SWCNT treatment further reduces the NLRP3-mediated IL-1β secretion in the infected cells. The results identify that a low-dose SWCNT treatment serves a protective function for the E. coli- and S. aureus-infected Caco-2 cells by negatively regulating mitochondrial reactive oxygen species-mediated NLRP3 inflammasome activation.
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Authors | Hanqing Chen, Bing Wang, Ruifang Zhao, Di Gao, Ming Guan, Lingna Zheng, Xiaoyan Zhou, Zhifang Chai, Yuliang Zhao, Weiyue Feng |
Journal | Small (Weinheim an der Bergstrasse, Germany)
(Small)
Vol. 11
Issue 34
Pg. 4366-78
(Sep 09 2015)
ISSN: 1613-6829 [Electronic] Germany |
PMID | 26097125
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- CARD Signaling Adaptor Proteins
- Carrier Proteins
- Cytoskeletal Proteins
- Inflammasomes
- Interleukin-1beta
- NLR Family, Pyrin Domain-Containing 3 Protein
- NLRP3 protein, human
- Nanotubes, Carbon
- PYCARD protein, human
- Reactive Oxygen Species
- Superoxides
- Caspase 1
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Topics |
- Bacterial Adhesion
- CARD Signaling Adaptor Proteins
- Caco-2 Cells
- Carrier Proteins
(genetics, metabolism)
- Caspase 1
(genetics, metabolism)
- Cell Shape
- Cell Survival
- Coculture Techniques
(methods)
- Cytoskeletal Proteins
(genetics, metabolism)
- Enterocytes
(microbiology, pathology)
- Epithelium
(pathology)
- Escherichia coli
(pathogenicity, ultrastructure)
- Humans
- Inflammasomes
(metabolism)
- Inflammation
(pathology)
- Interleukin-1beta
(metabolism)
- Microvilli
(ultrastructure)
- Mitochondria
(metabolism)
- NLR Family, Pyrin Domain-Containing 3 Protein
- Nanotubes, Carbon
(chemistry)
- Reactive Oxygen Species
(metabolism)
- Staphylococcus aureus
(pathogenicity, ultrastructure)
- Superoxides
(metabolism)
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