MicroRNA-124 expression in Kupffer cells modulates liver injury by targeting IL-6/STAT3 signaling

被引:4
|
作者
Wang, Jinyu [1 ]
Zhang, Xueyun [1 ]
Han, Jiajia [1 ]
Zhou, Pu [1 ]
Yu, Xueping [1 ]
Shen, Zhongliang [1 ]
Mao, Richeng [1 ]
Lu, Mengji [2 ]
Huang, Yuxian [1 ,3 ]
Zhang, Jiming [1 ,4 ,5 ,6 ,7 ]
机构
[1] Fudan Univ, Huashan Hosp, Shanghai Inst Infect Dis & Biosecur, Natl Med Ctr Infect Dis,Dept Infect Dis,Shanghai K, Shanghai, Peoples R China
[2] Univ Duisburg Essen, Univ Hosp Essen, Inst Virol, Essen, Germany
[3] Fudan Univ, Shanghai Publ Hlth Clin Ctr, Dept Hepatol, Shanghai, Peoples R China
[4] Fudan Univ, JingAn Branch Huashan Hosp, Dept Infect Dis, Shanghai, Peoples R China
[5] Fudan Univ, Shanghai Inst Infect Dis & Biosecur, Key Lab Med Mol Virol, Minist Educ, Shanghai, Peoples R China
[6] Fudan Univ, Minist Hlth MOH&MOE, Shanghai, Peoples R China
[7] Fudan Univ, Huashan Hosp, Dept Infect Dis, 12 Middle Wulumuqi Rd, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatitis B virus; Liver injury; Kupffer cells; microRNA-124; IL-6; SUPPORT-SYSTEMS; FAILURE; MACROPHAGES; HEPATITIS; ACTIVATION; POLARIZATION; HOMEOSTASIS; ONTOGENY; RESIDENT; DISTINCT;
D O I
10.1016/j.antiviral.2022.105510
中图分类号
R9 [药学];
学科分类号
1007 ;
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 inflam-mation 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 & PRIME;-untranslated region of signal transducer and activator of transcription 3 (STAT3) and inhibits IL-6/STAT3 signaling, which reduces pro-inflammatory Kupffer cell po-larization. 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.
引用
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页数:11
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