Abstract

Selectins belong to a group of adhesion molecules that fulfill an essential role in immune and inflammatory responses and tissue healing. Selectins are glycoproteins that decode the information carried by glycan structures, and non-covalent interactions of selectins with these glycan structures mediate biological processes. The sialylated and fucosylated tetrasaccharide sLex is an essential glycan recognized by selectins. Several glycosyltransferases are responsible for the biosynthesis of the sLex tetrasaccharide. Selectins are involved in a sequence of interactions of circulated leukocytes with endothelial cells in the blood called the adhesion cascade. Recently, it has become evident that cancer cells utilize a similar adhesion cascade to promote metastases. However, like Dr. Jekyll and Mr. Hyde’s two faces, selectins also contribute to tissue destruction during some infections and inflammatory diseases. The most prominent function of selectins is associated with the initial stage of the leukocyte adhesion cascade, in which selectin binding enables tethering and rolling. The first adhesive event occurs through specific non-covalent interactions between selectins and their ligands, with glycans functioning as an interface between leukocytes or cancer cells and the endothelium. Targeting these interactions remains a principal strategy aimed at developing new therapies for the treatment of immune and inflammatory disorders and cancer. In this review, we will survey the significant contributions to and the current status of the understanding of the structure of selectins and the role of selectins in various biological processes. The potential of selectins and their ligands as therapeutic targets in chronic and acute inflammatory diseases and cancer will also be discussed. We will emphasize the structural characteristic of selectins and the catalytic mechanisms of glycosyltransferases involved in the biosynthesis of glycan recognition determinants. Furthermore, recent achievements in the synthesis of selectin inhibitors will be reviewed with a focus on the various strategies used for the development of glycosyltransferase inhibitors, including substrate analog inhibitors and transition state analog inhibitors, which are based on knowledge of the catalytic mechanism.

Highlights

  • The adhesion of molecules, either among cells or between an immune cell and target cellular component of the extracellular matrix, is the crucial event in the physiological process

  • The C2GnT knock-out mice [136] showed that the binding of P- and L-selectin to leukocytes was almost entirely absent, and binding to E-selectin was diminished [137]. These results show that the action C2GnT-I transferase is important for the biosynthesis of P-selectin ligands, whereas for some mechanism in which a nucleophilic attack by O6 and the separation of the leaving group all occur almost simultaneously [135]

  • These results showed that PSGL-1 binding depends on ST3Gal-4, while ST3Gal-4 is not required for L-selectin ligand activity on high endothelial cells of Peyer’s patch high endothelial venules (HEV)

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Summary

Introduction

The adhesion of molecules, either among cells or between an immune cell and target cellular component of the extracellular matrix, is the crucial event in the physiological process. Selectins are cell membrane glycoproteins that mediate adhesion of hematopoietic and cancer cells to endothelial cells, leukocytes, and platelets in flowing blood [7,8,9]. These adhesion events play a crucial role in inflammation, infection, cancer, lymphocyte and bone marrow stem cell homing, and immune cell surveillance. In contrast to P- and E-selectin, L-selectin is constitutively expressed on lymphocytes, monocytes, and granulocytes and is cleaved from the cell surface after cell activation The selectins and their ligands have become therapeutic targets in the prevention or at least alleviation of various diseases, including cancer. Due to the complexity of the subject, only selected details are discussed, but detailed coverage of this complex and multidisciplinary area of research is outside of the scope of this review

The Structure of Selectins
Glycans as Minimal Recognition Determinants for Selectins
P-Selectin Ligands
E-Selectin Ligands
L-Selectin Ligands
Glycosyltransferases Involved in the Biosythesis of Glycan Determinants
The Glycosyltransferase Polypeptide UDP-GalNAc Transferase
The Biological Role of Selectins
Selectins in Inflammatory Processes
Mechanism of Selectin-Ligand Interaction
Selectins in Hemostasis and Thrombosis
Selectins in Cancer
Signaling Functions of Selectins and Selectin Ligands
The inhibition of Selectin-Ligand Interactions
Inhibition of the Expression of Selectins
Macromolecular Inhibitors
Non-Carbohydrate Inhibitors
Carbohydrate Processing Inhibitors
Substrate Analog Inhibitors
Non-Substrate Inhibitors
Summary and Perspectives
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