

Author: Ji L. Ito M. Zhang G. Hirabayashi Y. Inokuchi J-I. Yamagata T.
Publisher: Elsevier
ISSN: 0003-9861
Source: Archives of Biochemistry and Biophysics, Vol.359, Iss.1, 1998-11, pp. : 107-114
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Abstract
The glycosphingolipid content of HL60 cells was reduced by endoglycoceramidase, an enzyme which specifically hydrolyzes glycosphingolipids on the cell surface, or by d-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol, an inhibitor which specifically reduces the activity of UDP-glucose:ceramide glucosyltransferase. Reduction of the glycosphingolipid content by both reagents resulted in enhancement of glucose uptake and glycolysis. Neither of these effects was observed in the presence of cytochalasin B, an inhibitor of facilitated glucose transport. The uptake of radiolabeled 3-
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