低密度脂蛋白受体
胆固醇
家族性高胆固醇血症
受体
调节器
低密度脂蛋白
脂蛋白
生物
细胞生物学
内科学
内分泌学
医学
生物化学
基因
作者
Heidi M. Schmidt,Kelsey E. Jarrett,Thomas Q. de Aguiar Vallim,Elizabeth J. Tarling
标识
DOI:10.1161/circresaha.124.323578
摘要
Clearance of circulating plasma LDL (low-density lipoprotein) cholesterol by the liver requires hepatic LDLR (low-density lipoprotein receptor). Complete absence of functional LDLR manifests in severe hypercholesterolemia and premature atherosclerotic cardiovascular disease. Since the discovery of the LDLR 50 years ago by Brown and Goldstein, all approved lipid-lowering medications have been aimed at increasing the abundance and availability of LDLR on the surface of hepatocytes to promote the removal of LDL particles from the circulation. As such a critical regulator of circulating and cellular cholesterol, it is not surprising that LDLR activity is tightly regulated. Despite over half a century’s worth of study, there are still many facets of LDLR biology that remain unexplored. This review will focus on pathways that regulate the LDLR and emerging concepts of LDLR biology.
科研通智能强力驱动
Strongly Powered by AbleSci AI