肿瘤坏死因子α
促炎细胞因子
药理学
白细胞介素
巨噬细胞
癌症研究
p38丝裂原活化蛋白激酶
MAPK/ERK通路
信号转导
作者
Jie Yang,Lin Liu,Mengmeng Li,Xuemei Huang,Huanjie Yang,Kai Li
标识
DOI:10.1016/j.molimm.2021.07.003
摘要
Naringenin (Nar) is a flavanone that has been suggested to provide human health benefits such as anti-inflammatory, anti-oxidant and anti-cancer properties. However, the mechanisms underlying these benefits are complex and still not fully understood. In this study, we investigated the effect of Nar on the inflammatory response of macrophages and its underlying mechanism. In lipopolysaccharide (LPS)-stimulated human macrophages, Nar inhibited the activation of NF-κB pathway and suppressed the downstream expression of pro-inflammatory factors. In addition, Nar was also able to induce metallothionein 1 G (MT1G) expression, and the inhibitory effects of Nar on the production of pro-inflammatory cytokines was dependent on MT1G. Mechanistically, we found that MT1G-mediated inhibition of pro-inflammatory cytokines responses might be through repressing NF-κB activation via zinc chelation. Overall, this study reveals a novel mechanism of Nar on inflammatory responses, the suppression of NF-κB activation through upregulation of MT1G.
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