胆酸
胆汁酸
促红细胞生成素肝细胞(Eph)受体
EPH受体A2
受体
敌手
药理学
G蛋白偶联胆汁酸受体
化学
生物化学
生物活性
生物
熊去氧胆酸
受体拮抗剂
化学生物学
法尼甾体X受体
作用机理
对接(动物)
表型
细胞
结构-活动关系
微生物群
作者
Andrea Blesio,Carmine Giorgio,Francesca Romana Ferrari,Stefano Sala,Lisa Flammini,Ilaria Zanotti,Daniela Passeri,Antimo Gioiello,Lorenzo Sarcone,Riccardo Castelli,Kun Karnchanapandh,Federica Vacondio,Lorenzo Tagliazucchi,Laura Scalvini,Marco Mor.,Alessio Lodola,Massimiliano Tognolini
标识
DOI:10.1016/j.bcp.2026.117807
摘要
The role of the Eph/ephrin system is well recognized in various physiological and pathological processes, including acute inflammation and cancer. We previously discovered that the secondary bile acid lithocholic acid (LCA) is a competitive antagonist of Eph receptors. The utility of LCA as a pharmacological tool for investigating Eph/ephrin biology was hampered by its primary activity at the FXR and TGR5 receptors. A recent study of centenarians' gut microbiomes revealed that a rare bile acid closely related to LCA, isoallolithocholic acid (IALCA), exerts marked protective effects on the intestinal epithelium, but its specific molecular target was unidentified. Considering the well-documented involvement of EphA2 in regulating intestinal epithelial/endothelial permeability, we asked whether IALCA could act through this receptor. Molecular docking and dynamics simulations predicted that IALCA binds within the ephrin-A1-binding pocket of EphA2. Our findings were validated through wet experiments, and IALCA emerged as a selective EphA2 inhibitor, blocking ephrin-A1 binding with low-micromolar potency. In functional studies, IALCA inhibited ephrin-A1-induced EphA2 phosphorylation, cell retraction, and rounding, confirming its antagonistic activity. Moreover, IALCA showed no detectable activity at the classical bile-acid receptors FXR, PXR, LXRα, or TGR5, thereby potentially linking its cellular and phenotypic effects to modulation of the Eph-ephrin system. As a final step, we demonstrated that IALCA also provides an attractive template for synthesizing new Eph antagonists. Overall, this work underscores the potential of the human gut microbiome as a reservoir of privileged chemical scaffolds for both fundamental pharmacology and therapeutic drug development.
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