Abstract
Granulocyte colony-stimulating factor (G-CSF) receptor (G-CSFR) is a type I cytokine receptor which is involved in hematopoietic cell maturation. G-CSFR has three putative C-mannosylation sites at W253, W318, and W446; however, it is not elucidated whether G-CSFR is C-mannosylated or not. In this study, we first demonstrated that G-CSFR was C-mannosylated at only W318. We also revealed that C-mannosylation of G-CSFR affects G-CSF-dependent downstream signaling through changing ligand binding capability but not cell surface localization. Moreover, C-mannosylation of G-CSFR was functional and regulated granulocytic differentiation in myeloid 32D cells. In conclusion, we found that G-CSFR is C-mannosylated at W318 and that this C-mannosylation has role(s) for myeloid cell differentiation through regulating downstream signaling.
| Original language | English |
|---|---|
| Pages (from-to) | 466-472 |
| Number of pages | 7 |
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 498 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2018 Apr 6 |
Keywords
- C-mannosylation
- Glycosylation
- Granulocyte colony-stimulating factor receptor (G-CSFR)
- Mass spectrometry
- Myeloid differentiation
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology
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