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Biochemistry (Moscow)

, Volume 78, Issue 7, pp 736–745 | Cite as

Desialylation of surface receptors as a new dimension in cell signaling

  • A. V. PshezhetskyEmail author
  • L. I. Ashmarina
Review

Abstract

Terminal sialic acid residues are found in abundance in glycan chains of glycoproteins and glycolipids on the surface of all live cells forming an outer layer of the cell originally known as glycocalyx. Their presence affects the molecular properties and structure of glycoconjugates, modifying their function and interactions with other molecules. Consequently, the sialylation state of glycoproteins and glycolipids has been recognized as a critical factor modulating molecular recognitions inside the cell, between the cells, between the cells and the extracellular matrix, and between the cells and certain exogenous pathogens. Until recently sialyltransferases that catalyze transfer of sialic acid residues to the glycan chains in the process of their biosynthesis were thought to be mainly responsible for the creation and maintenance of a temporal and spatial diversity of sialylated moieties. However, the growing evidence suggests that in mammalian cells, at least equally important roles belong to sialidases/neuraminidases, which are located on the cell surface and in intracellular compartments, and may either initiate the catabolism of sialoglycoconjugates or just cleave their sialic acid residues, and thereby contribute to temporal changes in their structure and functions. The current review summarizes emerging data demonstrating that mammalian neuraminidase 1, well known for its lysosomal catabolic function, is also targeted to the cell surface and assumes the previously unrecognized role as a structural and functional modulator of cellular receptors.

Key words

sialylation neuraminidase lysosome plasma membrane immune response cell growth insulin 

Abbreviations

CathA

cathepsin A/protective protein

ddNeuAc

2,3-dehydro-2-deoxy-N-acetylneuraminic acid

EBP

elastin-binding protein

EGFR

epidermal growth factor receptor

FcγR

Fc receptors for immunoglobulin G

GAL

β-galactosidase

GS

galactosialidosis

IGF-II

insulin-like growth factor II

IFN

interferon

IL-4

interleukin 4

IR

insulin receptor

LAMP-1

lysosome associated membrane protein 1

LDL

low-density lipoprotein

LDLR

LDL receptor

LPS

lipopolysaccharide

MUC1

mucin 1

NEU1, −2, −3, −4

neuraminidase 1, −2, −3, −4

PDGF

platelet-derived growth factor

SGC

sialoglycoconjugate

Sia

sialic acid

Siglec

sialic acid binding immunoglobulin-like lectins

SMC

smooth muscle cells

Syk

serine-tyrosine kinase

TLR

Toll-like receptor

VLDL

very low density lipoprotein

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Supplementary material

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Copyright information

© Pleiades Publishing, Ltd. 2013

Authors and Affiliations

  1. 1.Department of Medical GeneticsCHU Sainte-Justine Research CenterMontrealCanada
  2. 2.Departments of Pediatrics and BiochemistryUniversity of MontrealMontrealCanada
  3. 3.Department of Anatomy and Cell Biology, Faculty of MedicineMcGill UniversityMontrealCanada

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