Role of Aberrant Sialylation of Chronic Myeloid Leukemia Granulocytes on Binding and Signal Transduction by Chemotactic Peptides and Colony Stimulating Factors

References

• Schiffmann E., Showell H. V., Corcoran B. A., Ward P. A., Smith E., Becker E. L. The Isolation and Partial Characterization of Neutrophil Chemotactic Factors from Escherichia coli. J. Immunol. 1975; 114: 1831–1837
   PubMed Web of Science ®Google Scholar
• Neidel J., Cuatrecasas P. Formyl Peptide Chemotactic Receptors of Leukocytes and Macrophages. Current Topics of Cellular Regulation 1981; 17: 137–170
   Google Scholar
• Snyderman R., Goetzel E. J. Molecular and Cellular Mechanisms of Leukocyte Chemotaxis. Science 1981; 213: 830–837
   PubMed Web of Science ®Google Scholar
• Cook N., Dexter T. M., Lord B. I., Cragoe E. J., Jr., Whetton A. D. Identification of a common signal associated with cellular proliferation stimulated by four hae-mopoietic growth factors in a highly enriched population of granulocyte/macrophage colony-forming cells. EMBO J. 1989; 8: 2967–2974
   PubMed Web of Science ®Google Scholar
• Just U., Stocking C., Spooncer E., Dexter T. M., Ostertag W. Expression of the GM-CSF gene after retroviral transfer in hematopoietic stem cell lines induces synchronous granulocyte-macrophage differentiation. Cell 1991; 64: 1163–1173
   PubMed Web of Science ®Google Scholar
• Morrissey P. J., Grabstein K. H., Reed S. G., Conlon P. J. Granulocyte/macrophage colony stimulating factor. A potent activation signal for mature macrophages and monocytes. Int. Arch. Allergy Appl. Immunol. 1989; 88: 40–45
   PubMedGoogle Scholar
• Verghese W. M., Smith C. D., Snyderman R. Potential Role for a Guanine Nucleotide Regulatory Protein in Chemoattractant Receptor Mediated Polyphosphoinositide Metabolism, Ca++ Mobilization and Cellular Responses by Leukocytes. Biochem. Biophys. Res. Comm. 1985; 127: 450–457
   PubMed Web of Science ®Google Scholar
• Molski T. F. P., Naccache P. H., Marsh M. L., Kermode J., Becker E. L., Sha'Affi R. L. Pertussis Toxin Inhibits the Rise in the Intracellular Concentration of Free Calcium that is Induced by Chemotactic Factors in Rabbit Neutrophils: Possible Role of the “G-Proteins” in Calcium Mobilization. Biochem. Biophys. Res. Comm. 1984; 124: 644–650
   PubMed Web of Science ®Google Scholar
• Lad P. M., Olsen C. V., Smiley P. A. Association of the N-formyl-Met-Leu-Phe Receptor in Human Neutrophils with a GTP Binding Protein Sensitive to Pertussis Toxin. Proc. Nat. Acad. Sci. USA 1985; 82: 869–873
   PubMed Web of Science ®Google Scholar
• Truett A. P., III, Verghese M. W., Dillon S. B., Snyderman R. Calcium Influx Stimulates a Second Pathway for Sustained Production in Leukocytes Activated by Chemoattractants. Proc. Nat. Acad. Sci. USA 1988; 85: 1549–1553
   PubMed Web of Science ®Google Scholar
• Korchak H. M., Vosshall L. B., Zagon G., Ljubich P., Rich A. M., Weissmann G. Activation of the Neutrophil by Calcium-mobilizing Ligands 1: A Chemotactic Peptide and the Lectin Concanavalin A Stimulate Superoxide Anion Generation but Elicit Different Calcium Movements and Phosphoinositide Remodelling. J. Biolog. Chem. 1988; 263: 11090–11097
   PubMed Web of Science ®Google Scholar
• Korchak H. M., Vosshall L. B., Haines K. A., Wilken-Feld C., Lundquist K. F., Weissmann G. Activation of the Neutrophil by Calcium-mobilizing Ligands II: Correlation of Calcium, Diacyl Glycerol, and Phosphatidic Acid Generation with Superoxide Anion Generation. J. Biolog. Chem. 1988; 263: 11098–11105
   PubMed Web of Science ®Google Scholar
• Huang K. C., Laramee R. G., Casnellie E. J. Chemotactic factor induced tyrosine phosphorylation of membrane associated proteins in rabbit peritoneal neutrophils. Biochem. Biophys. Res. Comm. 1988; 151: 794–801
   PubMed Web of Science ®Google Scholar
• Carroll M. P., Clark-Lewis L., Rapp U. R., May W. S. Interleukin-3 and granulocyte-macrophage colony-stimulating factor mediate rapid phosphorylation and activation of cytosolic c-raf. J. Biolog. Chem. 1990; 265: 19812–19817
   PubMed Web of Science ®Google Scholar
• Frank A. D., Sartorelli C. A. Alterations in tyrosine phosphorylation during the granulocytic maturation of HL-60 leukemia cells. Cancer Res. 1988; 48: 52–58
   PubMed Web of Science ®Google Scholar
• Athens J. W., Raab S. O., Haab O. P., Boggs D. R., Ash-Enbrucker H., Cartwright G. E., Wintrobe M. M. Blood granulocyte kinetics in chronic myelocytic leukemia. J. Clin. Investig. 1965; 44: 765
   PubMed Web of Science ®Google Scholar
• Everson M. P., Brown C. B., Lilly M. B. In-terleukin-6 and granulocyte-macrophage colony-stimulating factor are candidate growth factors for chronic myelomono-cytic leukemia cells. Blood. 1989; 74: 1472–1476
   PubMed Web of Science ®Google Scholar
• Baker M. A., Taub R. N., Kanani A., Brockhausen I., Hindenburg A. Increased Activity of a Specific Sialyltransferase in Chronic Myelogenous Leukemia. Blood 1985; 66(5)1068–1071
   PubMed Web of Science ®Google Scholar
• Baker M. A., Taub R. N., Kanani A., Brockhausen I., Hindenberg A. Unique Sialyl-transferase Activity in Chronic Myelogenous Leukaemia. Blood 1984; 64: 186a, (suppl.)
   Google Scholar
• Filipovic I. Effect of Inhibiting N-Glycosylation on the Stability and Binding Activity of the Low Density Lipo-protein Receptor. J. Biochem. 1989; 264(15)8815–8820
   Google Scholar
• Minegishi T., Delgado C., Duau M. L. Phos-phorylation and Glycosylation of the Luteinizing Hormone Receptor. Proc. Nat. Acad. Sci. USA 1989; 86: 1470–1474
   PubMed Web of Science ®Google Scholar
• Fischer T., Thoma B., Scheurich P., Pfizenmaier K. Glycosylation of the Human Interferon γ Receptor. J. Biolog. Chem. 1990; 265(3)1710–1717
   PubMed Web of Science ®Google Scholar
• Feige J. J., Baird A. Glycosylation of the Basic Fibroblast Growth Factor Receptor. J. Biolog. Chem. 1988; 263(28)14023–14029
   PubMed Web of Science ®Google Scholar
• Hubbard S. C., Kranz D. M., Longmore G. D., Sitkovsky M. V., Eisen H. N. Glycosylation of the T-cell Antigen Specific Receptor and its Role in Lectin-Mediated Cytotoxicity. Proc. Nat. Acad. Sci. USA 1986; 83: 1852–1856
   PubMed Web of Science ®Google Scholar
• Gearing D. P., King J. A., Gough N. M., Nicola N. A. Expression Cloning of a Receptor for Human Gran-ulocyte-Macrophage Colony-Stimulating Factor. The EMBO J. 1989; 8(12)3667–3676
   PubMed Web of Science ®Google Scholar
• Hayashida K., Kitamura T., Gorman D. M., Arai K. I., Yokota T., Miyajima A. Molecular Cloning of a Second Subunit of the Receptor for Human Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF): Recon-stitution of a High-Affinity GM-CSF Receptor. Proc. Nat. Acad. Sci. USA 1990; 87: 9655–9659
   PubMed Web of Science ®Google Scholar
• Shibuya K., Chiba S., Miyagawa K., Kitamura T., Mi-Yazono K., Takaku F. The Structural and Functional Analysis of Glycosylation on the Distinct Molecules of Human GM-CSF Receptors. Eur. J. Biochem. 1991; 198(3)659–666
   PubMedGoogle Scholar
• Malech H. L., Gardner J. P., Heiman D. F., Rosen-Zweig S. A. Asparagine-linked Oligosaccharides on Formyl Peptide Chemotactic Receptors of Human Phagocytic Cells. J. Biolog. Chem. 1985; 260(4)2509–2514
   PubMed Web of Science ®Google Scholar
• Taub R. N., Baker M. A., Madyastha K. R. Masking of Neutrophil Surface Lectin Binding sites in Chronic Myelogenous Leukemia. Blood 1980; 55: 294
   PubMed Web of Science ®Google Scholar
• Baker M. A., Kanani A., Brockhausen I., Schachter H., Hindenberg A., Taub R. N. Presence of Cytidine 5'-Monophospho-N-acetylneuraminic Acid:Gal β l -3Ga l Nac-R α(2–3)-Sialyltransferase in Normal Human Leukocytes and Increased Activity of This Enzyme in Grdnulocytes from Chronic Myelogenous Leukemia Patients. Cancer Res. 1987; 47: 2763–2766
   PubMed Web of Science ®Google Scholar
• Baker M. A., Kanani A., Hindenburg A., Taub R. N. Changes in the Granulocyte Membrane Following Chemotherapy for Chronic Myelogenous Leukaemia. Br. J. Haematol. 1986; 62: 431–438
   PubMed Web of Science ®Google Scholar
• Chaplinski T. J., Niedel J. E. Cyclic Nucleotidc-induced Maturation of Human Promyelocytic Leukemia Cells. J. Clin. Investig. 1982; 70(5)953–964
   PubMed Web of Science ®Google Scholar
• Gelfand E. W., Mills C. B., Cheung R. K., Lee J. W. W., Grinstein S. Transmembrane Ion Fluxes During Activation of Human T Lymphocytes-Role of Ca2+ Na' / H+ Exchange and Phospholipid Tumover. Immunol. Rev. 1987; 95: 59
   PubMed Web of Science ®Google Scholar
• Gelfand E. W., Cheung R. K., Mills G. B., Grinstein S. Role of Membrane Potential in the Response of Human T Lymphocytes to Phyto-hemagglutinin. J. Immunol. 1987; 138: 527
   PubMed Web of Science ®Google Scholar
• Grynkiewicz G., Poenie M., Lsien R. Y. A New Generation of Ca2+ Indicators With Greatly Improved Fluorescence Properties. J. Biolog. Chem. 1986; 260: 3440
   Web of Science ®Google Scholar
• Williams L. T., Snyderman R., Pike M. C., Letkow-Itz R. J. Specific Receptor Sites for Human Poly-morphonuclear Leukocytes. Proc. Nat. Acad. Sci. USA 1977; 74: 1204–1208
   PubMed Web of Science ®Google Scholar
• Kanani A., May C., Sutherland D. R., Hindenburg A., Taub R. N., Mills G. B., Baker M. A. Altered Rise of FMLP Stimulated Free Cytosolic Calcium [Ca2+]i in CML Granulocytes. Blood 1987; 70(5), (suppl)
   Google Scholar
• Baker M. A., Kanani A., Brockhausen I., Schachter H., Hindenberg A., Taub R. N. Presence of Cytidine 5'-Monophospho-N-acetylneuraminic Acid: Ga l βl -3GaI Nac-RaL(2–3)-Sialyltransferase in Normal Human Leukocytes and Increased Activity of This Enzyme in Granulocytes from Chronic Myelogenous Leukemia Patients. Cancer Res. 1987; 47: 2763–2766
   PubMed Web of Science ®Google Scholar
• Brockhausen I., Kuhnk W., Schachter H., Matta K. L., Sutherland D. R., Baker M. A. Biosynthesis of O-Glycans in Leukocytes from Normal Donors and from Patients with Leukemia: Increase in O-Glycan Core 2 UDP-GlcNAc:Gal β3GalNAcα-R (GlcNAc to GalNAc)β(1–6)-N-Acetylglucosaminyltrdnsferase in Leukemic Cells. Cancer Res. 1991; 51: 1257–1263
   PubMed Web of Science ®Google Scholar
• Perez H. D., Ong R. R., Elfman F. Removal or Oxidation of Surface Membrane Sialic Acid Inhibits-Formyl-Peptide-Induced Polymorphonuclear Leukocyte Chemotaxis. J. Immunol. 1985; 134(3)1902–1908
   PubMed Web of Science ®Google Scholar