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Sialic Acids As Regulators of Molecular and Cellular Interactions

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Date 2009 Aug 25
PMID 19699080
Citations 284
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Abstract

The wide occurrence of sialic acids (Sia) in various chemical forms linked as monomers or polymers in an outstanding position in a multitude of complex carbohydrates of animals and microorganisms renders them as most versatile function modulators in cell biology and pathology. A survey is presented of recent advances in the study of the influences that Sias have as bulky hydrophilic and electronegatively charged monosaccharides on animal cells and on their interaction with microorganisms. Some highlights are: sialylation leads to increased anti-inflammatory activity of IgG antibodies, facilitates the escape of microorganisms from the host's immune system, and in polymeric form is involved in the regulation of embryogenesis and neuronal growth and function. The role of siglecs in immunoregulation, the dynamics of lymphocyte binding to selectins and the interactions of toxins, viruses, and other microorganisms with the host's Sia are now better understood. N-Glycolylneuraminic acid from food is antigenic in man and seems to have pathogenic potential. Sia O-acetylation mediated by various eukaryotic and prokaryotic O-acetyltransferases modulates the affinity of these monosaccharides to mammalian and microbial receptors and hinders apoptosis. The functionally versatile O-acetylated ganglioside GD3 is an onco-fetal antigen.

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References
1.
Quarles R . Myelin-associated glycoprotein (MAG): past, present and beyond. J Neurochem. 2007; 100(6):1431-48. DOI: 10.1111/j.1471-4159.2006.04319.x. View

2.
von Itzstein M, Thomson R . Anti-influenza drugs: the development of sialidase inhibitors. Handb Exp Pharmacol. 2008; (189):111-54. DOI: 10.1007/978-3-540-79086-0_5. View

3.
Lehmann F, Kelm S, Dietz F, von Itzstein M, Tiralongo J . The evolution of galactose alpha2,3-sialyltransferase: Ciona intestinalis ST3GAL I/II and Takifugu rubripes ST3GAL II sialylate Galbeta1,3GalNAc structures on glycoproteins but not glycolipids. Glycoconj J. 2007; 25(4):323-34. DOI: 10.1007/s10719-007-9078-4. View

4.
Woronowicz A, Amith S, De Vusser K, Laroy W, Contreras R, Basta S . Dependence of neurotrophic factor activation of Trk tyrosine kinase receptors on cellular sialidase. Glycobiology. 2006; 17(1):10-24. DOI: 10.1093/glycob/cwl049. View

5.
Yao L, Korteweg C, Hsueh W, Gu J . Avian influenza receptor expression in H5N1-infected and noninfected human tissues. FASEB J. 2007; 22(3):733-40. DOI: 10.1096/fj.06-7880com. View