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Soyasaponin Bb inhibits the recruitment of toll‐like receptor 4 (TLR4) into lipid rafts and its signaling pathway by suppressing the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase‐dependent generation of reactive oxygen species
Author(s) -
Zhang Yajie,
Chen Fengping,
Chen Jiading,
Huang Suqun,
Chen Junbin,
Huang Jian,
Li Nan,
Sun Suxia,
Chu Xinwei,
Zha Longying
Publication year - 2016
Publication title -
molecular nutrition and food research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.495
H-Index - 131
eISSN - 1613-4133
pISSN - 1613-4125
DOI - 10.1002/mnfr.201600015
Subject(s) - lipid raft , nicotinamide adenine dinucleotide phosphate , nadph oxidase , trif , chemistry , tlr4 , reactive oxygen species , biochemistry , microbiology and biotechnology , toll like receptor , receptor , signal transduction , oxidase test , biology , innate immune system , enzyme
Scope We and others recently showed that soyasaponin Bb (SS Bb ) inhibited lipopolysaccharide (LPS)‐induced inflammation in macrophages. Since the recruitment of toll‐like receptor 4 (TLR4) into lipid rafts is vital for LPS‐initiated signaling, we investigated whether this process would be modulated by SS Bb . Methods and results By using sucrose gradient ultracentrifuge, we found that pretreatment of macrophages with SS Bb inhibited LPS‐induced recruitments of TLR4, myeloid differentiation primary response protein 88 (MyD88) and Toll/IL‐1 receptor domain‐containing adaptor inducing interferon‐β (TRIF) into fractions enriched with lipid rafts marker flotillin‐1. We also found SS Bb decreased co‐localization of TLR4 and lipid rafts by utilizing confocal immunofluorescence microscopy. Additionally, we observed that SS Bb suppressed LPS‐induced formation of TLR4/MyD88 and TLR4/TRIF complexes, production of pro‐inflammatory molecules, and activation of nuclear factor kappa B (NF‐κB). Furthermore, we found that these inhibitory effects of SS Bb were associated with reduced reactive oxygen species (ROS) because pretreating cells with N‐acetyl‐L‐cysteine and NADPH oxidase inhibitor diphenyleneiodonium (DPI) inhibited LPS‐induced TLR4 recruitment into lipid rafts and NF‐κB activation. SS Bb also inhibited NADPH oxidase activation by blocking interaction between gp91 phox and p47 phox similarly as DPI. Conclusion SS Bb can inhibit TLR4 recruitment into lipid rafts and its signaling by suppressing the NADPH oxidase‐dependent ROS generation.