姜黄素
TLR3型
内部收益率3
免疫系统
污渍
转录组
刺激
TLR5型
药理学
肿瘤坏死因子α
生物
化学
TLR4型
分子生物学
基因表达
免疫学
生物化学
先天免疫系统
基因
Toll样受体
TLR2型
内分泌学
作者
Xue Zhang,Liang Chen,Chun Hu,David J. Fast,Lu Zhang,Bong Min Yang,Juntao Kan,Jun Du
标识
DOI:10.1016/j.jff.2022.104949
摘要
Curcumin is widely used in dietary supplements due to its beneficial effects on inflammatory and immune pathways. To better understand the action of curcumin during viral infection, its effect on stimulation of RAW264.7 macrophages with polyinosinic-polycytidylic acid (poly(I:C)) was evaluated by deep sequencing transcriptome, followed by RT-qPCR, western blotting and ELISA validations. The transcriptomics results showed that 157 differentially expressed genes are in association with the activity of curcumin on the cellular response to poly(I:C) stimulation. Gene Ontology and KEGG enrichment analysis uncovered the involvement of TLRs, in particular TLR3, in curcumin’s effect on poly(I:C)-induced immune and inflammatory responses. RT-qPCR results showed that curcumin (2.5, 5, 10 μM) significantly down-regulated the mRNA expression of Tlr3, Irf-7, Ifnb1, Il-6, Tnfα, and Il1bf in a dose-dependent manner. Significant down-regulation of curcumin (5 M) on protein or phosphorylated protein expressions of TLR3 (p < 0.05), TBK1 (P < 0.005), IRF3 (P < 0.0005), IRF7 (p < 0.0005), IFN-β (P < 0.0005),TNF-α (P < 0.0001) and IL6 (P < 0.0001) were also observed in western blotting or ELISA results. Taken together, these results indicated that down-regulation on TLR3/TBK1/IFN-β cascade may involve in the underlying mechanism of curcumin alleviating virus-like infections. The findings from our study contribute to a better understanding of the action of curcumin during viral infection, suggesting the potential of curcumin preparations to support a healthy immune system.
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