下调和上调
肝星状细胞
基因敲除
糖酵解
化学
细胞生物学
厌氧糖酵解
转录因子
癌症研究
肝细胞
纤维化
肝纤维化
肝纤维化
亚细胞定位
转录组
肝损伤
生物
基因表达调控
信使核糖核酸
抄写(语言学)
内分泌学
作者
Ming Xiong,Shenan Huang,Y Li,Huan Cai
标识
DOI:10.1096/fj.202600255rr
摘要
ABSTRACT Abnormal glycolysis plays a pivotal role in the activation of hepatic stellate cells (HSCs) and the progression of liver fibrosis, yet its regulatory mechanisms remain incompletely understood. This study aimed to investigate the role of PIM2 and its regulatory mechanisms in liver fibrosis using a CCl 4 ‐induced mouse model and a TGF‐β1‐stimulated human HSC line (LX‐2) model. The results showed that PIM2 expression was significantly upregulated in fibrotic liver tissue and a specific subset of activated HSCs. Functional experiments showed that PIM2 knockdown suppressed the activation, proliferation, and glycolysis of this specific HSC subset, whereas PIM2 overexpression promoted these processes. These effects were reversed by the glycolysis inhibitor 2‐DG. Mechanistically, NUDT21 downregulation promoted PIM2 expression by regulating alternative polyadenylation (APA), resulting in PIM2 3′UTR shortening. Downstream, PIM2 activated the transcription factor CEBPB, which upregulated the transcription of the glucose transporter SLC2A1 and ultimately drove glycolysis. In line with these findings, PIM2 knockdown effectively attenuated liver fibrosis in mice. In conclusion, this study identifies PIM2 as a key driver of HSC activation and glycolysis within a distinct HSC subpopulation. PIM2 expression is regulated by NUDT21‐mediated APA, and its function is mediated via the CEBPB/SLC2A1 axis, providing a potential novel therapeutic target for liver fibrosis.
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