Ciechanover A, Schwartz A L, Lodish H F
J Cell Biochem. 1983;23(1-4):107-30. doi: 10.1002/jcb.240230111.
With few exceptions, receptor-mediated endocytosis of specific ligands is mediated through clustering of receptor-ligand complexes in coated pits on the cell surface, followed by internalization of the complex into endocytic vesicles. During this process, ligand-receptor dissociation occurs, most probably in a low pH prelysosomal compartment. In most cases the ligand is ultimately directed to the lysosomes, wherein it is degraded, while the receptor recycles to the cell surface. We have studied the kinetics of internalization and recycling of both the asialoglycoprotein receptor and the transferrin receptor in a human hepatoma cell line. By employing both biochemical and morphological/immunocytochemical approaches, we have gained some insight into the complex mechanisms which govern receptor recycling as well as ligand sorting and targeting. We can, in particular, explain why transferrin is exocytosed intact from the cells, while asialoglycoproteins are degraded in lysosomes. We have also localized the intracellular site at which endocytosed receptor and ligand dissociate.
除少数例外情况外,特定配体的受体介导的内吞作用是通过细胞表面被覆小窝中受体 - 配体复合物的聚集来介导的,随后复合物内化进入内吞小泡。在此过程中,配体 - 受体解离,最有可能发生在低pH的前溶酶体区室中。在大多数情况下,配体最终被导向溶酶体,在那里它被降解,而受体则循环回到细胞表面。我们研究了人肝癌细胞系中去唾液酸糖蛋白受体和转铁蛋白受体的内化和循环动力学。通过采用生化和形态学/免疫细胞化学方法,我们对控制受体循环以及配体分选和靶向的复杂机制有了一些了解。特别是,我们可以解释为什么转铁蛋白能完整地从细胞中胞吐出来,而去唾液酸糖蛋白却在溶酶体中被降解。我们还定位了内吞的受体和配体解离的细胞内位点。