Reid Mari V, Fredickson Gavin, Mashek Douglas G
Department of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Minneapolis, Minnesota, USA.
Department of Integrated Biology and Physiology, University of Minnesota, Minneapolis, Minnesota, USA.
Hepatology. 2024 Oct 30. doi: 10.1097/HEP.0000000000001141.
Hepatic steatosis, the buildup of neutral lipids in lipid droplets (LDs), is commonly referred to as metabolic dysfunction-associated steatotic liver disease when alcohol or viral infections are not involved. Metabolic dysfunction-associated steatotic liver disease encompasses simple steatosis and the more severe metabolic dysfunction-associated steatohepatitis, characterized by inflammation, hepatocyte injury, and fibrosis. Previously viewed as inert markers of disease, LDs are now understood to play active roles in disease etiology and have significant nonpathological and pathological functions in cell signaling and function. These dynamic properties of LDs are tightly regulated by hundreds of proteins that coat the LD surface, controlling lipid metabolism, trafficking, and signaling. The following review highlights various facets of LD biology with the primary goal of discussing key mechanisms through which LDs promote the development of advanced liver diseases, including metabolic dysfunction-associated steatohepatitis.
肝脂肪变性,即脂质在脂滴(LDs)中积累,在不涉及酒精或病毒感染时,通常被称为代谢功能障碍相关脂肪性肝病。代谢功能障碍相关脂肪性肝病包括单纯性脂肪变性以及更严重的代谢功能障碍相关脂肪性肝炎,其特征为炎症、肝细胞损伤和纤维化。脂滴以前被视为疾病的惰性标志物,现在人们认识到它在疾病病因中发挥着积极作用,并且在细胞信号传导和功能方面具有重要的非病理和病理功能。脂滴的这些动态特性受到数百种覆盖在脂滴表面的蛋白质的严格调控,这些蛋白质控制着脂质代谢、运输和信号传导。以下综述重点介绍了脂滴生物学的各个方面,主要目的是讨论脂滴促进晚期肝病(包括代谢功能障碍相关脂肪性肝炎)发展的关键机制。