Cellular and Chemical Biology Unit, Institut Curie, 75248 Paris Cedex 05, France
Cellular and Chemical Biology Unit, Institut Curie, 75248 Paris Cedex 05, France.
Cold Spring Harb Perspect Biol. 2024 Jan 2;16(1):a041398. doi: 10.1101/cshperspect.a041398.
Most cell surface proteins are decorated by glycans, and the plasma membrane is rich in glycosylated lipids. The mechanisms by which the enormous complexity of these glycan structures on proteins and lipids is exploited to control glycoprotein activity by setting their cell surface residence time and the ways by which they are taken up into cells are still under active investigation. Here, two mechanisms are presented, termed galectin lattices and glycolipid-lectin (GL-Lect)-driven endocytosis, which are among the most prominent to establish a link between glycan information and endocytosis. Types of glycans on glycoproteins and glycolipids are reviewed from the angle of their interaction with glycan-binding proteins that are at the heart of galectin lattices and GL-Lect-driven endocytosis. Examples are given to show how these mechanisms affect cellular functions ranging from cell migration and signaling to vascularization and immune modulation. Finally, outstanding challenges on the link between glycosylation and endocytosis are discussed.
大多数细胞表面蛋白都被聚糖修饰,而质膜富含糖基化脂质。目前,人们正在积极研究蛋白质和脂质上这些聚糖结构的巨大复杂性是如何被利用来控制糖蛋白活性的,具体机制为控制糖蛋白在细胞表面的停留时间以及它们进入细胞的方式。在这里,提出了两种机制,即半乳糖凝集素晶格和糖脂-凝集素(GL-Lect)驱动的内吞作用,它们是将糖链信息与内吞作用联系起来的最主要机制之一。本文从糖结合蛋白的角度综述了糖蛋白和糖脂上的聚糖类型,这些糖结合蛋白是半乳糖凝集素晶格和 GL-Lect 驱动的内吞作用的核心。本文还举例说明了这些机制如何影响细胞功能,范围从细胞迁移和信号转导到血管生成和免疫调节。最后,讨论了糖基化与内吞作用之间联系的尚未解决的挑战。