Schnaar Ronald L
Department of Pharmacology and Molecular Science and the Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Md.
J Allergy Clin Immunol. 2015 Mar;135(3):609-15. doi: 10.1016/j.jaci.2014.10.057. Epub 2015 Jan 30.
Cells are endowed with a rich surface coat of glycans that are carried as glycoproteins and glycolipids on the outer leaflets of their plasma membranes and constitute a major molecular interface between cells and their environment. Each cell's glycome, the sum of its diverse glycan structures, comprises a distinct cellular signature defined by expression levels of the enzymes responsible for glycan biosynthesis. This signature can be read by complementary glycan-binding proteins (GBPs) that translate glycan recognition into function. Nowhere is this more evident than in the immune system, where glycans and GBPs are integral to pathogen recognition and control of inflammatory responses. Glycobiology, the study of glycan structures and their functions, increasingly provides insight into immunoregulatory mechanisms and thereby provides opportunities for therapeutic intervention. This review briefly examines the makeup of the human glycome and the GBPs that translate glycan recognition into function and provides examples of glycan recognition events that are responsible for immune system regulation to promote wider appreciation of this rapidly expanding area of research.
细胞被赋予了一层丰富的聚糖表面涂层,这些聚糖以糖蛋白和糖脂的形式存在于其质膜的外小叶上,构成了细胞与其环境之间的主要分子界面。每个细胞的糖组,即其多样聚糖结构的总和,包含由负责聚糖生物合成的酶的表达水平所定义的独特细胞特征。这种特征可以被互补的聚糖结合蛋白(GBP)识别,这些蛋白将聚糖识别转化为功能。这在免疫系统中最为明显,在那里聚糖和GBP对于病原体识别和炎症反应的控制不可或缺。糖生物学,即对聚糖结构及其功能的研究,越来越多地为免疫调节机制提供见解,从而为治疗干预提供机会。本综述简要考察了人类糖组的组成以及将聚糖识别转化为功能的GBP,并提供了负责免疫系统调节的聚糖识别事件的例子,以促进对这一迅速扩展的研究领域的更广泛认识。