Zhou Yutong, Sun Yong, Yin Pengsheng, Zuo Shi, Li Haiyang, Cao Kun
Department of Hepatobiliary Surgery, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Key Laboratory of Hepatobiliary and Pancreatic Diseases Treatment and Bioinformatics Research, Guizhou Medical University, Guiyang, China.
Front Cell Infect Microbiol. 2025 Jun 20;15:1620829. doi: 10.3389/fcimb.2025.1620829. eCollection 2025.
Bacterial Extracellular Vesicles (BEVs) are key mediators of cross-talk between gut microorganisms and host organs, playing an especially important role in the gut-liver axis. In this paper, we systematically review the mechanisms of BEV production, their classification, and their regulatory networks in liver diseases. BEVs carry pathogenic factors such as lipopolysaccharide (LPS) and bacterial DNA, which can enter the circulatory system by disrupting the intestinal barrier and target the liver to induce metabolic abnormalities, including insulin resistance. Furthermore, through activation of signaling pathways such as LPS/TLR4, cGAS/STING, and TGF-β, BEVs promote the progression of metabolism-associated fatty liver disease (MAFLD), liver fibrosis, and hepatocellular carcinoma. In addition, BEVs show dual potential in the diagnosis and treatment of liver diseases: on one hand, they can be used as non-invasive biomarkers to enhance diagnostic specificity through multi-omics analysis; on the other hand, engineered and modified BEVs, as well as probiotic BEVs (e.g., from and species), can regulate lipid metabolism, reduce inflammation, and even enhance immunotherapy by targeting the tumor microenvironment. However, the heterogeneity of BEVs, efficient isolation techniques, storage stability, and clinical translation remain major challenges in current research. In the future, combining multi-omics techniques to resolve the molecular fingerprints of BEVs, optimizing isolation methods, and exploring their potential as precision medicine tools will be necessary to advance the study of the gut-liver axis toward clinical applications.
细菌细胞外囊泡(BEVs)是肠道微生物与宿主器官之间相互作用的关键介质,在肠-肝轴中发挥着尤为重要的作用。在本文中,我们系统地综述了BEV的产生机制、分类及其在肝脏疾病中的调控网络。BEVs携带脂多糖(LPS)和细菌DNA等致病因子,这些因子可通过破坏肠道屏障进入循环系统,并靶向肝脏诱导代谢异常,包括胰岛素抵抗。此外,通过激活LPS/TLR4、cGAS/STING和TGF-β等信号通路,BEVs促进代谢相关脂肪性肝病(MAFLD)、肝纤维化和肝细胞癌的进展。此外,BEVs在肝脏疾病的诊断和治疗中显示出双重潜力:一方面,它们可用作非侵入性生物标志物,通过多组学分析提高诊断特异性;另一方面,工程化和修饰的BEVs以及益生菌BEVs(例如来自 和 物种)可调节脂质代谢、减轻炎症,甚至通过靶向肿瘤微环境增强免疫治疗。然而,BEVs的异质性、高效分离技术、储存稳定性和临床转化仍是当前研究中的主要挑战。未来,结合多组学技术解析BEVs的分子指纹、优化分离方法并探索其作为精准医学工具的潜力,对于推动肠-肝轴研究向临床应用发展至关重要。