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受体介导的内吞作用的分子和细胞机制。

Molecular and cellular mechanisms of receptor-mediated endocytosis.

作者信息

Brown V I, Greene M I

机构信息

Department of Pathology, University of Pennsylvania, Philadelphia 19104.

出版信息

DNA Cell Biol. 1991 Jul-Aug;10(6):399-409. doi: 10.1089/dna.1991.10.399.

Abstract

In general, receptors are involved in pathways of endocytosis, either constitutive or ligand induced. These receptors cluster in clathrin-coated pits, enter the cell via clathrin-coated vesicles, pass through an acidified endosome in which the receptors and ligands are sorted, and then either recycle to the cell surface, become stored intracellularly, or are degraded in lysosomes. The internalization pathways serve a variety of functions, such as nutrient uptake, removal of activated proteins, clearance of macromolecules, opportunistic entry of certain viruses and toxins, dissociation and degradation of ligand, and receptor-level regulation. Many receptors follow more than one intracellular pathway, depending on the cell type, receptor concentration, type of ligand, ligand valency, and ligand concentration. Although endocytosis is common to all nucleated eukaryotic cells, the factors that regulate these receptor-mediated endocytic pathways are not fully understood. Defective receptors that are not capable of undergoing normal endocytosis can lead to certain disease states, as in the case of familial hypercholesteremia (FH). This review has three objectives: (i) to describe the different routes that receptors and ligands follow after internaliation; (ii) to describe the potential mechanisms which regulate the initiation and subsequent sorting of receptors and ligands so they reach their final destination; and (iii) to describe the potential functions of receptor-mediated endocytosis.

摘要

一般来说,受体参与组成型或配体诱导型的内吞作用途径。这些受体聚集在网格蛋白包被的小窝中,通过网格蛋白包被的囊泡进入细胞,穿过一个酸化的内体,在其中受体和配体被分选,然后要么循环回到细胞表面,要么储存在细胞内,要么在溶酶体中降解。内化途径具有多种功能,如营养物质摄取、活化蛋白的清除、大分子的清除、某些病毒和毒素的机会性进入、配体的解离和降解以及受体水平的调节。许多受体遵循不止一种细胞内途径,这取决于细胞类型、受体浓度、配体类型、配体价态和配体浓度。虽然内吞作用在所有有核真核细胞中都很常见,但调节这些受体介导的内吞途径的因素尚未完全了解。不能进行正常内吞作用的缺陷受体可导致某些疾病状态,如家族性高胆固醇血症(FH)。本综述有三个目标:(i)描述内化后受体和配体遵循的不同途径;(ii)描述调节受体和配体起始及后续分选从而使其到达最终目的地的潜在机制;(iii)描述受体介导的内吞作用的潜在功能。

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