MAPK/ERK通路
Toll样受体
激酶
受体
信号转导
细胞因子
医学
细胞外
炎症
免疫学
细胞生物学
生物
内科学
先天免疫系统
作者
Qian Zhang,Qinqin Pu,Zhengyi Jiang,Jie Zhao,Yan Dai,Nannan Hu,Yaping Han,Nan Jiang,Luchen Shi,Jiaying Zhao,Ke Ouyang,Huaying Huang,Ke Jin,Jun Li
摘要
ABSTRACT Severe fever with thrombocytopenia syndrome (SFTS) is a severe emerging infectious disease caused by Dabie bandavirus (DBV). Tectorigenin has been demonstrated to exert anti‐inflammatory effect. Here, we aimed to investigate the effects of tectorigenin on DBV‐induced cytokine storm. Effects of tectorigenin on cytokines in DBV‐infected THP‐1 cells and plasma samples of Type I interferon receptor (IFNAR) −/− mice infected with DBV were detected. The changes in body weight and survival time of mice were recorded. The liver, spleen, kidney, and lymph node tissues were collected for hematoxylin–eosin staining. We demonstrated that tectorigenin reduced the expression levels of inflammatory cytokines in both DBV‐infected THP‐1 cells and plasma samples of IFNAR −/− mice infected with DBV. Tectorigenin attenuated DBV‐induced histopathological changes in mice. Mechanistically, tectorigenin attenuated DBV‐induced phosphorylation of inhibitor of kappa‐B kinase alpha/beta (IKKα/β) of the nuclear factor‐κB (NF‐κB) signaling pathway, extracellular signal–regulated kinase (ERK) of the mitogen‐activated protein kinase (MAPK) signaling pathway and might function by downregulation of Toll‐like receptor. The result of this study suggested that tectorigenin exerted anti‐inflammatory effects in vivo and in vitro and could serve as a novel potential therapeutic strategy for SFTS.
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