车站3
肝损伤
小RNA
库普弗电池
STAT蛋白
炎症
医学
乙型肝炎病毒
白细胞介素6
免疫学
癌症研究
细胞因子
信号转导
生物
内科学
病毒
细胞生物学
基因
生物化学
作者
Jinyu Wang,Xueyun Zhang,Jiajia Han,Pu Zhou,Xueping Yu,Zhongliang Shen,Richeng Mao,Mengji Lu,Yuxian Huang,Jiming Zhang
标识
DOI:10.1016/j.antiviral.2022.105510
摘要
MicroRNA-124 (miR-124) is related to liver injury due to chronic hepatitis B (CHB) and hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF). However, the mechanism whereby miR-124 regulates liver inflammation remains unknown. In this study, we show that serum miR-124 serves as a compensatory predictive factor for organ failure and the 28-day prognosis of patients with HBV-ACLF. Moreover, within a mouse model of concanavalin A-induced acute liver injury, miR-124 is highly expressed in Kupffer cells. Overexpression of miR-124 significantly decreases interleukin-6 (IL-6) secretion, and relieves pathological liver necrosis to a great extent. Mechanistically, miR-124 directly targets the 3′-untranslated region of signal transducer and activator of transcription 3 (STAT3) and inhibits IL-6/STAT3 signaling, which reduces pro-inflammatory Kupffer cell polarization. Collectively, our findings suggest that miR-124 can potentially serve as a predictive biomarker for HBV-ACLF prognosis and may represent a promising therapeutic target for relieving severe liver injury resulting from cytokine storms.
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