Windler E
Medizinische Kernklinik und Poliklinik, Universitäts-Krankenhaus Eppendorf, Hamburg.
Klin Wochenschr. 1990;68 Suppl 22:19-22.
The liver supplies peripheral tissues with lipoproteins containing triglycerides, a source of energy, and cholesterol, a structural component of cell membranes. The liver is also capable of taking up lipoproteins and excreting cholesterol in the bile. Because of this unique metabolic role the endocytosis of lipoproteins by the liver was studied. Lipoproteins bind through their component proteins to the low density lipoprotein-receptor of hepatocytes. Apolipoprotein B of low density lipoproteins exhibits fairly low affinity, whereas apolipoprotein E of the postlipolytic remnants of very low density lipoproteins and chylomicrons bind with much higher affinity, which results in a much shorter residence time of these lipoproteins in plasma. Premature uptake is prevented by the C-apolipoproteins, yet. Changes in the phospholipid composition of the lipoproteins during the intraplasmatic lipolysis lead to loss of C-apolipoproteins enabling interaction of apolipoprotein E with the receptors of the liver. Binding is followed by endocytosis into endosomes, which fuse to multivesicular bodies. The contents gets catabolized by hydrolytic enzymes of lysosomes thus becoming available to the cell.
肝脏向周围组织提供含有甘油三酯(一种能量来源)和胆固醇(细胞膜的一种结构成分)的脂蛋白。肝脏还能够摄取脂蛋白并将胆固醇排泄到胆汁中。由于肝脏具有这种独特的代谢作用,因此对肝脏摄取脂蛋白的内吞作用进行了研究。脂蛋白通过其组成蛋白与肝细胞的低密度脂蛋白受体结合。低密度脂蛋白的载脂蛋白B表现出相当低的亲和力,而极低密度脂蛋白和乳糜微粒的脂解后残余物中的载脂蛋白E则以高得多的亲和力结合,这导致这些脂蛋白在血浆中的停留时间短得多。不过,C-载脂蛋白可防止过早摄取。血浆内脂解过程中脂蛋白磷脂组成的变化导致C-载脂蛋白丢失,使载脂蛋白E能够与肝脏受体相互作用。结合之后是内吞作用进入内体,内体融合形成多囊体。其内容物被溶酶体的水解酶分解代谢,从而可供细胞利用。