Povero Davide, Feldstein Ariel E
Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Rady's Children Hospital, University of California San Diego, San Diego, CA, USA.
Diabetes Metab J. 2016 Feb;40(1):1-11. doi: 10.4093/dmj.2016.40.1.1.
Non-alcoholic fatty liver disease (NAFLD) is one of the most common causes of chronic liver disease in adults and children worldwide. NAFLD has become a severe health issue and it can progress towards a more severe form of the disease, the non-alcoholic steatohepatitis (NASH). A combination of environmental factors, host genetics, and gut microbiota leads to excessive accumulation of lipids in the liver (steatosis), which may result in lipotoxicity and trigger hepatocyte cell death, liver inflammation, fibrosis, and pathological angiogenesis. NASH can further progress towards liver cirrhosis and cancer. Over the last few years, cell-derived extracellular vesicles (EVs) have been identified as effective cell-to-cell messengers that transfer several bioactive molecules in target cells, modulating the pathogenesis and progression of NASH. In this review, we focused on recently highlighted aspects of molecular pathogenesis of NASH, mediated by EVs via their bioactive components. The studies included in this review summarize the state of art regarding the role of EVs during the progression of NASH and bring novel insight about the potential use of EVs for diagnosis and therapeutic strategies for patients with this disease.
非酒精性脂肪性肝病(NAFLD)是全球成人和儿童慢性肝病最常见的病因之一。NAFLD已成为一个严重的健康问题,并且它可能会进展为更严重的疾病形式,即非酒精性脂肪性肝炎(NASH)。环境因素、宿主遗传学和肠道微生物群的共同作用导致肝脏中脂质过度积累(脂肪变性),这可能导致脂毒性并引发肝细胞死亡、肝脏炎症、纤维化和病理性血管生成。NASH可进一步发展为肝硬化和癌症。在过去几年中,细胞衍生的细胞外囊泡(EVs)已被确定为有效的细胞间信使,可在靶细胞中传递多种生物活性分子,调节NASH的发病机制和进展。在本综述中,我们重点关注了由EVs通过其生物活性成分介导的NASH分子发病机制中最近突出的方面。本综述中纳入的研究总结了关于EVs在NASH进展过程中作用的最新进展,并为EVs在该疾病患者诊断和治疗策略中的潜在应用带来了新的见解。