TY - JOUR
T1 - Colonic mucus-accumulating tungsten oxide nanoparticles improve the colitis therapy by targeting Enterobacteriaceae
AU - Qin, Yuting
AU - Zhao, Ruifang
AU - Qin, Hao
AU - Chen, Long
AU - Chen, Hanqing
AU - Zhao, Yuliang
AU - Nie, Guangjun
N1 - Funding Information:
This work was supported by grants from the National Basic Research Plan of China ( 2018YFA0208900 , 2018YFE0205300 , and 2016YFA0201600 ), the National Natural Science Foundation of China ( 31800799 , 31730032 , 31820103004 , 11621505 ), and the K.C. Wong Education Foundation ( GJTD-2018-03 ).
Publisher Copyright:
© 2021
PY - 2021/8
Y1 - 2021/8
N2 - The imbalance of gut microbiota, such as dysbiotic expansion of Enterobacteriaceae, is strongly associated with the progress of inflammatory bowel disease (IBD) via exacerbating gut inflammation and disturbing intestinal mucosal barrier. Recently, a microbiota-based strategy is an attractive paradigm for IBD therapy. Here, we explored the therapeutic potential of tungsten oxide nanoparticles (WO3NPs) against DSS-induced acute colitis mice. WO3NPs (47.9 nm in diameter) significantly reduced intestinal inflammation, attenuated bacterial translocation, restored the colonic epithelium barriers, and remodeled gut microbiota homeostasis in inflamed colon, compared with the free tungsten (sodium tungstate). The element quantification and mapping results showed WO3NPs could increase the adherence of tungsten with Enterobacteriaceae in colonic mucus layer, which inhibited Enterobacteriaceae growth by microbial metabolic reprogramming and ameliorate colitis. This nano-enabled approach for tungsten reduced its deposition in the main organ except for the colon thereby improve the therapeutic efficacy with good biosafety. Together, our results provide insights into the potential nanotherapeutics of WO3NPs against the invasion processes of microbiota in the treatment of IBD.
AB - The imbalance of gut microbiota, such as dysbiotic expansion of Enterobacteriaceae, is strongly associated with the progress of inflammatory bowel disease (IBD) via exacerbating gut inflammation and disturbing intestinal mucosal barrier. Recently, a microbiota-based strategy is an attractive paradigm for IBD therapy. Here, we explored the therapeutic potential of tungsten oxide nanoparticles (WO3NPs) against DSS-induced acute colitis mice. WO3NPs (47.9 nm in diameter) significantly reduced intestinal inflammation, attenuated bacterial translocation, restored the colonic epithelium barriers, and remodeled gut microbiota homeostasis in inflamed colon, compared with the free tungsten (sodium tungstate). The element quantification and mapping results showed WO3NPs could increase the adherence of tungsten with Enterobacteriaceae in colonic mucus layer, which inhibited Enterobacteriaceae growth by microbial metabolic reprogramming and ameliorate colitis. This nano-enabled approach for tungsten reduced its deposition in the main organ except for the colon thereby improve the therapeutic efficacy with good biosafety. Together, our results provide insights into the potential nanotherapeutics of WO3NPs against the invasion processes of microbiota in the treatment of IBD.
KW - Bacterial respiration and energy metabolism
KW - Colonic mucus targeting
KW - Enterobacteriaceae
KW - Inflammatory bowel disease
KW - Tungsten oxide nanoparticles
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U2 - 10.1016/j.nantod.2021.101234
DO - 10.1016/j.nantod.2021.101234
M3 - Article
AN - SCOPUS:85108259036
SN - 1748-0132
VL - 39
JO - Nano Today
JF - Nano Today
M1 - 101234
ER -