Zou Xue, Brigstock David
Center for Clinical and Translational Research, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH 43205, USA.
Department of Surgery, Wexner Medical Center, The Ohio State University, Columbus, OH 43212, USA.
Biomedicines. 2024 Dec 14;12(12):2848. doi: 10.3390/biomedicines12122848.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by the accumulation of triglycerides within hepatocytes, which can progress to more severe conditions, such as metabolic dysfunction-associated steatohepatitis (MASH), which may include progressive fibrosis, leading to cirrhosis, cancer, and death. This goal of this review is to highlight recent research showing the potential of mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) in reducing the key pathogenic pathways of MASLD or MASH. Relevant published studies were identified using PubMed with one or more of the following search terms: MASLD, MASH, NAFLD, NASH, exosome, extracellular vesicle (EV), therapy, and/or mesenchymal stem cells (MSC). The primary literature were subsequently downloaded and summarized. Using in vitro or in vivo models, MSC-EVs have been found to counteract oxidative stress, a significant contributor to liver injury in MASH, and to suppress disease progression, including steatosis, inflammation, and, in a few instances, fibrosis. Some of these outcomes have been attributed to specific EV cargo components including microRNAs and proteins. Thus, MSC-EVs enriched with these types of molecules may have improved the therapeutic efficacy for MASLD/MASH and represent a novel approach to potentially halt or reverse the disease process. MSC-EVs are attractive therapeutic agents for treating MASLD/MASH. Further studies are necessary to validate the clinical applicability and efficacy of MSC-EVs in human MASH patients, focusing on optimizing delivery strategies and identifying the pathogenic pathways that are targeted by specific EV components.
代谢功能障碍相关脂肪性肝病(MASLD)的特征是肝细胞内甘油三酯的积累,这种情况可能会进展为更严重的病症,如代谢功能障碍相关脂肪性肝炎(MASH),后者可能包括进行性纤维化,进而导致肝硬化、癌症和死亡。本综述的目的是强调最近的研究,这些研究表明间充质干细胞衍生的细胞外囊泡(MSC-EVs)在减少MASLD或MASH关键致病途径方面的潜力。使用PubMed并通过以下一个或多个搜索词来识别相关的已发表研究:MASLD、MASH、非酒精性脂肪性肝病(NAFLD)、非酒精性脂肪性肝炎(NASH)、外泌体、细胞外囊泡(EV)、治疗和/或间充质干细胞(MSC)。随后下载并总结了主要文献。利用体外或体内模型,已发现MSC-EVs可对抗氧化应激(MASH中肝损伤的一个重要促成因素)并抑制疾病进展,包括脂肪变性、炎症,在少数情况下还可抑制纤维化。其中一些结果归因于特定的细胞外囊泡货物成分,包括微小RNA和蛋白质。因此,富含这些类型分子的MSC-EVs可能提高了对MASLD/MASH的治疗效果,并代表了一种潜在的阻止或逆转疾病进程的新方法。MSC-EVs是治疗MASLD/MASH的有吸引力的治疗剂。有必要进一步研究以验证MSC-EVs在人类MASH患者中的临床适用性和疗效,重点是优化递送策略并确定特定细胞外囊泡成分所靶向的致病途径。