Title of article :
Comparative Study of Glycosyltransferase Activities in Caco-2 Cells before and after Enterocytic Differentiation Using Lectin-Affinity High-Performance Liquid Chromatography
Author/Authors :
Amano، نويسنده , , Junko and Kobayashi، نويسنده , , Keiko and Oshima، نويسنده , , Mieko، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Abstract :
Human colonic adenocarcinoma Caco-2 cells differentiate into enterocytes by induction with sodium butyrate after confluence. Our previous studies have shown that there are high levels of H type 1 blood group antigen and core 2 structure present in O-glycans of the glycoproteins from these differentiated cells and these O-glycans appear to be indispensable for the process of differentiation of the cells (J. Amano and M. Oshima, 1999, J. Biol. Chem. 274, 21209–21216). Here, we have determined the glycosyltransferase activities using lectin-affinity HPLC because the method enabled easy separation and identification of mixtures of isomeric oligosaccharide structures due to the high resolution and reproducibility. The activities of β3-galactosyltransferase, α2-fucosyltransferase, which are responsible for H type 1 antigen biosynthesis, and core 2 β6-N-acetylglucosaminyltransferase in differentiated Caco-2 cells were higher than those in undifferentiated cells. These results demonstrate that an increase in specific glycosyltransferase activities brought on a change of the O-glycan structures during differentiation.
Keywords :
Caco-2 cells , Differentiation , enterocytes , glycosyltransferases , lectin-affinity HPLC
Journal title :
Archives of Biochemistry and Biophysics
Journal title :
Archives of Biochemistry and Biophysics