Barth J L, Argraves W S
Department of Cell Biology and Anatomy, Medical University of South Carolina, Charleston, SC 29425-2204, USA.
Trends Cardiovasc Med. 2001 Jan;11(1):26-31. doi: 10.1016/s1050-1738(01)00080-9.
Members of the low-density lipoprotein receptor (LDLR) family are unrivalled for their ability to endocytose and target ligands to lysosomes for degradation. Their endocytic and catabolic functions make them essential to homeostatic regulation of the level and activity of their ligands in biological fluids and interstitial spaces. Over the last few years it has become evident that the endocytic function of members of the LDLR family is employed by other kinds of cell surface receptors. Recently, the low-density lipoprotein receptor related protein-2 (megalin) was shown to act in concert with cubilin, a receptor for high-density lipoproteins (HDL)/apolipoprotein A-I (apoA-I), intrinsic factor-vitamin B12 and albumin to mediate ligand endocytosis. In this article, we review the state of knowledge pertaining to cubilin and megalin, emphasizing their joint roles in both lipoprotein and vitamin metabolism.
低密度脂蛋白受体(LDLR)家族成员在将配体进行内吞并靶向溶酶体进行降解的能力方面无与伦比。它们的内吞和分解代谢功能使其对于生物体液和组织间隙中配体水平及活性的稳态调节至关重要。在过去几年中,很明显LDLR家族成员的内吞功能被其他种类的细胞表面受体所利用。最近,低密度脂蛋白受体相关蛋白2(巨膜蛋白)被证明与立方体细胞蛋白协同作用,立方体细胞蛋白是高密度脂蛋白(HDL)/载脂蛋白A-I(apoA-I)、内因子-维生素B12和白蛋白的受体,以介导配体内吞作用。在本文中,我们综述了与立方体细胞蛋白和巨膜蛋白相关的知识现状,重点强调它们在脂蛋白和维生素代谢中的共同作用。