N-glycosylation of the human granulocyte-macrophage colony-stimulating factor receptor α subunit is essential for ligand binding and signal transduction Journal Article


Authors: Ding, D. X. H.; Vera, J. C.; Heaney, M. L.; Golde, D. W.
Article Title: N-glycosylation of the human granulocyte-macrophage colony-stimulating factor receptor α subunit is essential for ligand binding and signal transduction
Abstract: The α subunit of the receptor for human granulocyte-macrophage colony- stimulating factor (GM-CSF) is a glycoprotein containing 11 potential N- glycosylation sites in the extracellular domain. We examined the role of N- glycosylation on α subunit membrane localization and function. Tunicamycin, an N-glycosylation inhibitor, markedly inhibited GM-CSF binding, GM-CSF- induced deoxyglucose uptake, and protein tyrosine phosphorylation in HL- 60(eos) cells but did not affect cell surface expression of the α subunit as detected by an anti-α subunit monoclonal antibody. In COS cells expressing the α subunit and treated with tunicamycin, N-unglycosylated α subunit was expressed and transported to the cell surface but was not capable of binding GM-CSF. High affinity binding in COS cells expressing both α and β subunits was also blocked by tunicamycin treatment. These studies indicate that N- linked oligosaccharides are essential for α subunit ligand binding and signaling by the human GM-CSF receptor.
Keywords: signal transduction; protein phosphorylation; human cell; binding affinity; protein localization; animal; granulocyte macrophage colony stimulating factor; cell line; transfection; cercopithecus aethiops; endoplasmic reticulum; kinetics; recombinant proteins; cell membrane; glycosylation; immunoblotting; ligands; binding site; protein folding; antigen binding; ligand binding; granulocyte-macrophage colony-stimulating factor; hl-60 cells; receptors, granulocyte-macrophage colony-stimulating factor; tunicamycin; human; priority journal; article; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; macromolecular systems
Journal Title: Journal of Biological Chemistry
Volume: 270
Issue: 41
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1995-10-13
Start Page: 24580
End Page: 24584
Language: English
DOI: 10.1074/jbc.270.41.24580
PUBMED: 7592677
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 28 August 2018 -- Source: Scopus
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  1. Juan C Vera
    64 Vera
  2. Mark L Heaney
    94 Heaney
  3. David Golde
    127 Golde