Lopez Dayami
Department of Experimental Therapeutics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Biochim Biophys Acta. 2008 Apr;1781(4):184-91. doi: 10.1016/j.bbalip.2008.01.003. Epub 2008 Feb 2.
Proprotein convertase subtilisin/kexin type 9 (PCSK9) plays a critical role in cholesterol metabolism by controlling the levels of low density lipoprotein (LDL) particles that circulate in the bloodstream. Several gain-of-function and loss-of-function mutations in the PCSK9 gene, that occur naturally, have been identified and linked to hypercholesterolemia and hypocholesterolemia, respectively. PCSK9 expression has been shown to be regulated by sterol regulatory element binding proteins (SREBPs) and statins similar to other genes involved in cholesterol homeostasis. The most critical finding concerning PCSK9 is that this protease is able to influence the number of LDL receptor molecules expressed on the cell surface. Studies have demonstrated that PCSK9 acts mainly by enhancing degradation of LDL receptor protein in the liver. Inactivation of PCSK9 in mice reduces plasma cholesterol levels primarily by increasing hepatic expression of LDL receptor protein and thereby accelerating clearance of circulating LDL cholesterol. The objective of this review is to summarize the current information related to the regulation and function of PCSK9 and to identify gaps in our present knowledge.
前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)通过控制血液中循环的低密度脂蛋白(LDL)颗粒水平,在胆固醇代谢中发挥关键作用。已鉴定出PCSK9基因中自然发生的几种功能获得性和功能丧失性突变,分别与高胆固醇血症和低胆固醇血症相关。与其他参与胆固醇稳态的基因类似,PCSK9的表达已被证明受固醇调节元件结合蛋白(SREBPs)和他汀类药物调控。关于PCSK9最关键的发现是,这种蛋白酶能够影响细胞表面表达的LDL受体分子数量。研究表明,PCSK9主要通过增强肝脏中LDL受体蛋白的降解发挥作用。小鼠体内PCSK9的失活主要通过增加肝脏中LDL受体蛋白的表达,从而加速循环LDL胆固醇的清除,降低血浆胆固醇水平。本综述的目的是总结与PCSK9调控和功能相关的当前信息,并找出我们现有知识中的空白。