Induction of a storage phenotype and abnormal intracellular localization of apical glycoproteins are two independent responses to GalNAcalpha-O-bn

J Histochem Cytochem. 2003 Mar;51(3):349-61. doi: 10.1177/002215540305100310.

Abstract

Our previous studies on an inhibitor of O-glycosylation of glycoproteins, GalNAcalpha-O-bn, in the model of enterocytic HT-29 cells, have shown at the cellular level an alteration of the normal localization of apical glycoproteins, and at the biochemical level an in situ synthesis and storage of sialylated GalNAcalpha-O-bn oligosaccharides. The purpose of this study was to examine if a relation existed between these two events, using different cell lines. Intracellular storage of GalNAcalpha-O-bn metabolites occurred in HT-29 and CAPAN-1 cells but not in Caco-2 cells. On the other hand, an accumulation of endosomal/lysosomal compartments was observed in HT-29 and CAPAN-1 cells but not in Caco-2 cells. These data focused on a GalNAcalpha-O-bn-derived storage phenotype in HT-29 and CAPAN-1 cells. The apical membrane glycoproteins MUC1 and CEA showed an abnormal localization inside intracytoplasmic vesicles in HT-29 cells, whereas they kept their normal localization in Caco-2 and CAPAN-1 cells. Studies on the glycosylation of these apical glycoproteins showed that GalNAcalpha-O-bn inhibited the glycosylation in a cell-specific manner. The alteration in the apical targeting of glycoproteins, and the appearance of a GalNAcalpha-O-bn-derived storage phenotype are two independent and cell type-specific events. The former depends on the inhibition pattern of the glycosylation of endogenous glycoproteins, whereas the latter is connected to the intracellular accumulation of GalNAcalpha-O-bn metabolites.

MeSH terms

  • Antigens / metabolism
  • Antigens, Neoplasm
  • Carcinoembryonic Antigen / metabolism
  • Cell Line
  • Cell Polarity
  • Endosomes / metabolism
  • Galactose / analogs & derivatives
  • Galactose / metabolism*
  • Glycoproteins / metabolism*
  • Glycosylation
  • Humans
  • Immunohistochemistry
  • Kinetics
  • Lysosomes / metabolism
  • Microscopy, Confocal
  • Microscopy, Electron
  • Microscopy, Fluorescence
  • Mucin-1
  • Mucins

Substances

  • 1-benzyl-2-acetamido-2-galactopyranoside
  • Antigens
  • Antigens, Neoplasm
  • Carcinoembryonic Antigen
  • Glycoproteins
  • MUC1 protein, human
  • Mucin-1
  • Mucins
  • Galactose