肝星状细胞
细胞外基质
非酒精性脂肪肝
免疫系统
肝纤维化
肝损伤
纤维化
生物
癌症研究
细胞生物学
医学
病理
免疫学
脂肪肝
疾病
内分泌学
作者
Reham M. Dawood,Mai Abd El-Meguid,Ghada M. Salum,Mostafa K. El Awady
标识
DOI:10.1089/jir.2020.0059
摘要
Hepatic fibrosis is a complex mechanism defined by the net deposition of the extracellular matrix (ECM) owing to liver injury caused by multiple etiologies such as viral hepatitis and nonalcoholic fatty liver disease. Many cell types are implicated in liver fibrosis development and progression. In general, liver fibrosis starts with the recruitment of inflammatory immune cells to generate cytokines, growth factors, and other activator molecules. Such chemical mediators drive the hepatic stellate cells (HSCs) to activate the production of the ECM component. The activation of HSC is thus a crucial event in the fibrosis initiation, and a significant contributor to collagen deposition (specifically type I). This review explores the causes and mechanisms of hepatic fibrosis and focuses on the roles of key molecules involved in liver fibro genesis, some of which are potential targets for therapeutics to hamper liver fibro genesis.
科研通智能强力驱动
Strongly Powered by AbleSci AI