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STING 通过表观遗传激活 NLRP3 炎性小体介导肝纤维化中的肝细胞细胞焦亡。

STING mediates hepatocyte pyroptosis in liver fibrosis by Epigenetically activating the NLRP3 inflammasome.

机构信息

Lab of Gastroenterology and Hepatology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China; Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu, China.

Department of Biliary Surgery, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Redox Biol. 2023 Jun;62:102691. doi: 10.1016/j.redox.2023.102691. Epub 2023 Mar 29.

Abstract

The activation of stimulator of interferon genes (STING) and NOD-like receptor protein 3 (NLRP3) inflammasome-mediated pyroptosis signaling pathways represent two distinct central mechanisms in liver disease. However, the interconnections between these two pathways and the epigenetic regulation of the STING-NLRP3 axis in hepatocyte pyroptosis during liver fibrosis remain unknown. STING and NLRP3 inflammasome signaling pathways are activated in fibrotic livers but are suppressed by Sting knockout. Sting knockout ameliorated hepatic pyroptosis, inflammation, and fibrosis. In vitro, STING induces pyroptosis in primary murine hepatocytes by activating the NLRP3 inflammasome. H3K4-specific histone methyltransferase WD repeat-containing protein 5 (WDR5) and DOT1-like histone H3K79 methyltransferase (DOT1L) are identified to regulate NLRP3 expression in STING-overexpressing AML12 hepatocytes. WDR5/DOT1L-mediated histone methylation enhances interferon regulatory transcription factor 3 (IRF3) binding to the Nlrp3 promoter and promotes STING-induced Nlrp3 transcription in hepatocytes. Moreover, hepatocyte-specific Nlrp3 deletion and downstream Gasdermin D (Gsdmd) knockout attenuate hepatic pyroptosis, inflammation, and fibrosis. RNA-sequencing and metabolomics analysis in murine livers and primary hepatocytes show that oxidative stress and metabolic reprogramming might participate in NLRP3-mediated hepatocyte pyroptosis and liver fibrosis. The STING-NLRP3-GSDMD axis inhibition suppresses hepatic ROS generation. In conclusion, this study describes a novel epigenetic mechanism by which the STING-WDR5/DOT1L/IRF3-NLRP3 signaling pathway enhances hepatocyte pyroptosis and hepatic inflammation in liver fibrosis.

摘要

干扰素基因刺激物 (STING) 和 NOD 样受体蛋白 3 (NLRP3) 炎性体介导的细胞焦亡信号通路的激活代表了肝病中的两个不同的核心机制。然而,这些通路之间的联系以及在肝纤维化过程中肝细胞焦亡中 STING-NLRP3 轴的表观遗传调控仍然未知。STING 和 NLRP3 炎性体信号通路在纤维化肝脏中被激活,但被 Sting 敲除抑制。Sting 敲除改善了肝细胞焦亡、炎症和纤维化。在体外,STING 通过激活 NLRP3 炎性体在原代小鼠肝细胞中诱导细胞焦亡。发现组蛋白 H3K4 特异性甲基转移酶 WD 重复蛋白 5 (WDR5) 和 DOT1 样组蛋白 H3K79 甲基转移酶 (DOT1L) 可调节 STING 过表达 AML12 肝细胞中 NLRP3 的表达。WDR5/DOT1L 介导的组蛋白甲基化增强干扰素调节转录因子 3 (IRF3) 与 Nlrp3 启动子的结合,并促进 STING 诱导的肝细胞中 Nlrp3 转录。此外,肝细胞特异性 Nlrp3 缺失和下游 Gasdermin D (Gsdmd) 敲除可减轻肝细胞焦亡、炎症和纤维化。在小鼠肝脏和原代肝细胞中的 RNA 测序和代谢组学分析表明,氧化应激和代谢重编程可能参与 NLRP3 介导的肝细胞焦亡和肝纤维化。STING-NLRP3-GSDMD 轴抑制可抑制肝 ROS 生成。总之,本研究描述了一种新的表观遗传机制,即 STING-WDR5/DOT1L/IRF3-NLRP3 信号通路增强肝纤维化中肝细胞焦亡和肝炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8ea/10106968/984ca71f8046/ga1.jpg

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