Wang Jing, Bao Shuoqiang, An Qi, Li Caihong, Feng Juan
School of Public Health, Gansu University of Chinese Medicine, Lanzhou, China.
College of Health Science and Environmental Engineering, Shenzhen Technology University, Shenzhen, China.
Front Immunol. 2025 Mar 10;16:1544012. doi: 10.3389/fimmu.2025.1544012. eCollection 2025.
Metabolic-Associated Fatty Liver Disease (MAFLD) is the most common chronic liver disease worldwide, associated with systemic metabolic dysregulation. It can progress from simple hepatic steatosis (MAFL) to more severe conditions like Metabolic-Associated Steatohepatitis (MASH), fibrosis, cirrhosis, and Hepatocellular Carcinoma (HCC). There is a critical lack of reliable non-invasive diagnostic methods and effective pharmaceutical treatments for MAFLD/MASH, emphasizing the need for further research. Extracellular vesicles (EVs) are nanoscale structures that play important roles in cell signaling by delivering bioactive molecules. However, there is a significant gap in literature regarding the roles of EVs from hosts, plants, and microbiota in MAFLD. This review explores the potential of EVs from various sources-host, plants, and microbiota-as biomarkers, therapeutic agents, drug carriers, and treatment targets for MAFLD. Firstly, the roles of host-derived extracellular vesicles (EVs) in MAFLD, with a focus on cell-type specific EVs and their components-proteins, miRNAs, and lipids-for disease diagnosis and monitoring were discussed. Moreover, it highlighted the therapeutic potential of mesenchymal stem cell (MSC)-derived EVs in reducing lipid accumulation and liver injury, and immune cell-derived EVs in mitigating inflammation and fibrosis. The review also discussed the use of host-derived EVs as drug carriers and therapeutic targets due to their ability to deliver bioactive molecules that impact disease mechanisms. Additionally, it summarized research on plant-derived EVs, which help reduce liver lipid accumulation, inflammation, and enhance gut barrier function in MAFLD. Also, the review explored microbial-derived EVs as novel therapeutic targets, particularly in relation to insulin resistance, liver inflammation, and dysfunction in MAFLD. Overall, by exploring the diverse roles of EVs from host, plant, and microbiota sources in MAFLD, this review offers valuable insights into their potential as non-invasive biomarkers and novel therapeutic strategies, which could pave the way for more effective diagnostic and treatment options for this increasingly prevalent liver disease. Notably, the challenges of translating EVs into clinical practice were also thoroughly discussed, aiming to provide possible directions and strategies for future research.
代谢相关脂肪性肝病(MAFLD)是全球最常见的慢性肝病,与全身代谢失调有关。它可以从单纯性肝脂肪变性(MAFL)发展为更严重的疾病,如代谢相关脂肪性肝炎(MASH)、纤维化、肝硬化和肝细胞癌(HCC)。目前严重缺乏针对MAFLD/MASH的可靠非侵入性诊断方法和有效的药物治疗,这凸显了进一步研究的必要性。细胞外囊泡(EVs)是纳米级结构,通过传递生物活性分子在细胞信号传导中发挥重要作用。然而,关于宿主、植物和微生物群来源的EVs在MAFLD中的作用,文献中存在显著空白。本综述探讨了来自各种来源——宿主、植物和微生物群——的EVs作为MAFLD的生物标志物、治疗剂、药物载体和治疗靶点的潜力。首先,讨论了宿主来源的细胞外囊泡(EVs)在MAFLD中的作用,重点关注细胞类型特异性EVs及其成分——蛋白质、miRNA和脂质——在疾病诊断和监测中的应用。此外,它强调了间充质干细胞(MSC)来源的EVs在减少脂质积累和肝损伤方面的治疗潜力,以及免疫细胞来源的EVs在减轻炎症和纤维化方面的治疗潜力。该综述还讨论了宿主来源的EVs作为药物载体和治疗靶点的用途,因为它们能够传递影响疾病机制的生物活性分子。此外,它总结了植物来源的EVs的研究,这些EVs有助于减少MAFLD中的肝脏脂质积累、炎症,并增强肠道屏障功能。此外,该综述还探讨了微生物来源的EVs作为新型治疗靶点的作用,特别是在MAFLD中的胰岛素抵抗、肝脏炎症和功能障碍方面。总体而言,通过探讨宿主、植物和微生物群来源的EVs在MAFLD中的多种作用,本综述为它们作为非侵入性生物标志物和新型治疗策略的潜力提供了有价值的见解,这可能为这种日益普遍的肝病开辟更有效的诊断和治疗选择。值得注意的是,还深入讨论了将EVs转化为临床实践的挑战,旨在为未来研究提供可能的方向和策略。