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干扰素调节因子在肝脏疾病中的作用。

The Role of Interferon Regulatory Factors in Liver Diseases.

机构信息

Department of Gastroenterology, Renmin Hospital of Wuhan University, No. 99 Zhang Zhidong Road, Wuhan 430060, China.

出版信息

Int J Mol Sci. 2024 Jun 22;25(13):6874. doi: 10.3390/ijms25136874.

Abstract

The interferon regulatory factors (IRFs) family comprises 11 members that are involved in various biological processes such as antiviral defense, cell proliferation regulation, differentiation, and apoptosis. Recent studies have highlighted the roles of IRF1-9 in a range of liver diseases, including hepatic ischemia-reperfusion injury (IRI), alcohol-induced liver injury, Con A-induced liver injury, nonalcoholic fatty liver disease (NAFLD), cirrhosis, and hepatocellular carcinoma (HCC). IRF1 is involved in the progression of hepatic IRI through signaling pathways such as PIAS1/NFATc1/HDAC1/IRF1/p38 MAPK and IRF1/JNK. The regulation of downstream IL-12, IL-15, p21, p38, HMGB1, JNK, Beclin1, β-catenin, caspase 3, caspase 8, IFN-γ, IFN-β and other genes are involved in the progression of hepatic IRI, and in the development of HCC through the regulation of PD-L1, IL-6, IL-8, CXCL1, CXCL10, and CXCR3. In addition, IRF3-PPP2R1B and IRF4-FSTL1-DIP2A/CD14 pathways are involved in the development of NAFLD. Other members of the IRF family also play moderately important functions in different liver diseases. Therefore, given the significance of IRFs in liver diseases and the lack of a comprehensive compilation of their molecular mechanisms in different liver diseases, this review is dedicated to exploring the molecular mechanisms of IRFs in various liver diseases.

摘要

干扰素调节因子 (IRF) 家族由 11 个成员组成,参与多种生物学过程,如抗病毒防御、细胞增殖调节、分化和凋亡。最近的研究强调了 IRF1-9 在一系列肝脏疾病中的作用,包括肝缺血再灌注损伤 (IRI)、酒精性肝损伤、Con A 诱导的肝损伤、非酒精性脂肪性肝病 (NAFLD)、肝硬化和肝细胞癌 (HCC)。IRF1 通过 PIAS1/NFATc1/HDAC1/IRF1/p38 MAPK 和 IRF1/JNK 等信号通路参与肝 IRI 的进展。下游 IL-12、IL-15、p21、p38、HMGB1、JNK、Beclin1、β-catenin、caspase 3、caspase 8、IFN-γ、IFN-β 和其他基因的调节参与肝 IRI 的进展,并通过调节 PD-L1、IL-6、IL-8、CXCL1、CXCL10 和 CXCR3 参与 HCC 的发展。此外,IRF3-PPP2R1B 和 IRF4-FSTL1-DIP2A/CD14 途径参与 NAFLD 的发展。IRF 家族的其他成员在不同的肝脏疾病中也发挥着中等重要的作用。因此,鉴于 IRFs 在肝脏疾病中的重要意义以及缺乏对其在不同肝脏疾病中分子机制的全面汇编,本综述旨在探讨 IRFs 在各种肝脏疾病中的分子机制。

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