组蛋白
肝星状细胞
化学
下调和上调
细胞生物学
己糖激酶
乙酰化
微阵列分析技术
生物化学
亚细胞定位
糖酵解
癌症研究
基因表达
酶
小RNA
基因表达调控
基因
细胞
组蛋白H4
微阵列
分子生物学
作者
Tian Lan,Chenchen Wang,Junjie Ying,W F Wang,Xi-xi Zeng,Wei-Li Mao,Tao Lu,Siwei Wang
标识
DOI:10.1096/fj.202504035r
摘要
Hexokinase 2 (HK2) is a pivotal enzyme in glycolytic metabolism and plays a crucial role in the activation of hepatic stellate cells (HSCs). Despite its importance, specific inhibitors targeting HK2 are still lacking in clinical practice. In this study, we utilized a human protein microarray to identify a significant interaction between limonin (Lim) and HK2. Subsequent analyses confirmed that Lim effectively inhibits HK2 activity and the modification of histone lactylation. Moreover, Lim's systemic effects include the downregulation of gene expression associated with HSC activation, which is closely linked to its modulation of HK2 and histone lactylation. Additionally, Lim exhibits anti-fibrotic properties, influencing the expression of genes involved in HSC activation and histone lactylation in vivo. These findings provide novel mechanistic insights into how Lim derivatives may mitigate hepatic fibrosis through the suppression of HK2 and targeted regulation of histone lactylation in activated HSCs.
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