APOPTOTIC MODIFICATION OF GLYCOSPHINGOLIPIDS OF HUMAN GRANULOCYTES
DOI: http://dx.doi.org/10.30970/sbi.0602.220
Abstract
The phenomenon of programmed apoptotic desialylation of cell glycans was described previously. However, the possibility of this process application to the sialylated glycolipids of membranes stayes unknown. Granulocytes of human peripherical blood were utilized as a model for studying glycosphingolipid spectra changes. Ganglioside fractions were extracted from the granulocytes and purified by two-stage column chromatography – DEAE-Fractogel and Sephadex LH-20 sorbents, with subsequent analysis by thin-layer and high-performance liquid chromatography. An increased level of GM2, GM1 ganglioside and Gb3 globoside in apoptotic cells, as well as a decrease of GM3, GT3 and Gb4 amount were detected. These results draw to a conclusion that gangliosides, as well as N-glycans, might be a target of apoptotic desialylation. According to available recent data, changes in gangliosides can serve as important pathogenesis factors in the autoimmune disorders.
Keywords
Full Text:
PDF (Українська)References
1. Lopez P.H., Schnaar R.L. Gangliosides in cell recognition and membrane protein regulation. Curr. Opin. Struct. Biol, 2009; 19(5): 549-57. | |
| |
2. Nicoll G., Avril T., Lock K. et al. Ganglioside GD3 expression on target cells can modulate NK cell cytotoxicity via siglec-7-dependent and -independent mechanisms. Eur. J. Immunol, 2003; 33(6): 1642-8. | |
| |
3. Yoon S.J., Nakayama K., Hikita T. et al. Epidermal growth factor receptor tyrosine kinase is modulated by GM3 interaction with N-linked GlcNAc termini of the receptor. Proc. Natl. Acad. Sci. USA, 2006; 103(50): 18987-91. | |
| |
4. Nojiri H., Stroud M., Hakomori S. A specific type of ganglioside as a modulator of insulin-dependent cell growth and insulin receptor tyrosine kinase activity. Possible association of ganglioside-induced inhibition of insulin receptor function and monocytic differentiation induction in HL-60 cells. J. Biol. Chem, 1991; 266(7): 4531-7. | |
| |
5. Kolter T., Proia R.L., Sandhoff K. Combinatorial ganglioside biosynthesis. J. Biol. Chem, 2002; 277(29): 25859-62. | |
| |
6. Bilyy R.O., Shkandina T., Tomin A. et al. Macrophages discriminate glycosylation patterns of apoptotic cell-derived microparticles. J. Biol. Chem, 2012; 287(1): 496-503. | |
| |
7. Traving C., Schauer R. Structure, function and metabolism of sialic acids. Cell Mol. Life Sci, 1998; 54(12): 1330-49. | |
| |
8. Schauer R. Sialic acids as regulators of molecular and cellular interactions. Curr. Opin. Struct. Biol, 2009; 19(5): 507-14. | |
| |
9. Ledeen R.W., Wu G., Andre S. et al. Beyond glycoproteins as galectin counterreceptors: effector T cell growth control of tumors via ganglioside GM1. Ann. NY Acad. Sci, 2012; 1253: 206-21. | |
| |
10. Uncini A. A common mechanism and a new categorization for anti-ganglioside antibody-mediated neuropathies. Exp. Neurol, 2012; 235(2): 513-6. | |
| |
11. Labrador-Horrillo M., Martinez-Valle F., Gallardo E. et al. Anti-ganglioside antibodies in patients with systemic lupus erythematosus and neurological manifestations. Lupus, 2012; 21(6): 611-5. | |
| |
12. Bilyy R., Tomin A., Mahorivska I. et al. Antibody-mediated sialidase activity in blood serum of patients with multiple myeloma. J. Mol. Recognit, 2011; 24(4): 576-84. | |
| |
13. Bilyy R., Tomin A., Tolstyak Ya. et al. Cell Surface Glycans at SLE - Changes During Cells Death, Utilization for Disease Detection and Molecular Mechanism Underlying Their Modification. Autoimmune Disorders - Pathogenetic Aspects, 2011: 89-110. | |
| |
14. Haslett C., Guthrie L.A., Kopaniak M.M. et al. Modulation of multiple neutrophil functions by preparative methods or trace concentrations of bacterial lipopolysaccharide. Am. J. Pathol, 1985; 119(1): 101-10. | |
| |
15. Newman S.L., Henson J.E., Henson P.M. Phagocytosis of senescent neutrophils by human monocyte-derived macrophages and rabbit inflammatory macrophages. J. Exp. Med, 1982; 156(2): 430-42. | |
| |
16. Suzuki K., Poduslo S.E., Norton W.T. Gangliosides in the myelin fraction of developing rats. Biochim. Biophys. Acta, 1967; 144(2): 375-81. | |
| |
17. Yu R.K., Ariga T. Ganglioside analysis by high-performance thin-layer chromatography. Methods Enzymol, 2000; 312: 115-34. | |
| |
18. Svennerholm L. Chromatographic Separation of Human Brain Gangliosides. J. Neurochem, 1963; 10: 613-23. | |
| |
19. Hayakawa T., Hirai M. An assay of ganglioside using fluorescence image analysis on a thin-layer chromatography plate. Anal. Chem, 2003; 75(23): 6728-31. | |
| |
20. Svennerholm L. The Gangliosides. J. Lipid Res, 1964; 5: 145-55. | |
| |
21. Fredman P., Nilsson O., Tayot J.L., Svennerholm L. Separation of gangliosides on a new type of anion-exchange resin. Biochim. Biophys. Acta, 1980; 618(1): 42-52. | |
| |
22. Norris-Cervetto E., Callaghan R., Platt F.M., Dwek R.A., Butters T.D. Inhibition of glucosylceramide synthase does not reverse drug resistance in cancer cells. J. Biol. Chem, 2004; 279(39): 40412-8. | |
| |
23. Bigge J.C., Patel T.P., Bruce J.A. et al. Nonselective and efficient fluorescent labeling of glycans using 2-amino benzamide and anthranilic acid. Anal. Biochem, 1995; 230(2): 229-38. | |
| |
24. Monti E., Bassi M.T., Papini N. et al. Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane. Biochem. J, 2000; 349(Pt 1): 343-51. | |
| |
25. Ullmannova V., Haskovec C. The use of housekeeping genes (HKG) as an internal control for the detection of gene expression by quantitative real-time RT-PCR. Folia Biol. (Praha), 2003; 49(6): 211-6. | |
| |
26. Papini N., Anastasia L., Tringali C. et al. The plasma membrane-associated sialidase MmNEU3 modifies the ganglioside pattern of adjacent cells supporting its involvement in cell-to-cell interactions. J. Biol. Chem, 2004; 279(17): 16989-95. |
Refbacks
- There are currently no refbacks.
Copyright (c) 2012 Studia biologica
This work is licensed under a Creative Commons Attribution 4.0 International License.