Initiation of altered heparan sulphate on beta-D-xyloside in rat hepatocytes

Hoppe Seylers Z Physiol Chem. 1981 Jan;362(1):39-46. doi: 10.1515/bchm2.1981.362.1.39.

Abstract

Inhibition of protein synthesis by cycloheximide 10(-3)M reduced the incorporation of [35S]sulphate into heparan sulphate to about 5% of untreated hepatocytes. Addition of rho-nitrophenyl beta-D-xyloside could partially revert this inhibitory effect. The sulphated material isolated from the cell layer or secretions of hepatocytes grown in presence of cycloheximide and rho-nitrophenyl beta-D-xyloside were shown to be mostly free heparan sulphate chains not bound to core protein. Covalent association of beta-xylosides to the heparan sulphates was demonstrated for heparan sulphate synthetized in the presence of [35S]sulphate, cycloheximide and the fluorogenic 4-methylumbelliferyl beta-D-xyloside. Beta-Xylosides served as an initiator of heparan sulphate chain synthesis in rat hepatocytes only in the absence of protein synthesis. Heparan sulphates primed on artificial beta-xylosides are slightly smaller in molecular size and are more sulphated than chains linked to core protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cycloheximide / pharmacology
  • Glycosaminoglycans / biosynthesis*
  • Glycosides / pharmacology*
  • Heparitin Sulfate / biosynthesis*
  • Liver / drug effects
  • Liver / metabolism*
  • Rats
  • Sulfur Radioisotopes
  • Tritium

Substances

  • Glycosaminoglycans
  • Glycosides
  • Sulfur Radioisotopes
  • Tritium
  • 4-nitrophenyl beta-D-xyloside
  • Heparitin Sulfate
  • Cycloheximide