Sulfation in the Golgi lumen of Madin-Darby canine kidney cells is inhibited by brefeldin A and depends on a factor present in the cytoplasm and on Golgi membranes

J Biol Chem. 2002 Sep 27;277(39):36272-9. doi: 10.1074/jbc.M206365200. Epub 2002 Jul 22.

Abstract

Madin-Darby canine kidney cells are more resistant than most other cell types to the classical effects of brefeldin A (BFA) treatment, the induction of retrograde transport of Golgi cisternae components to the endoplasmic reticulum. Here we show that sulfation of heparan sulfate proteoglycans (HSPGs), chondroitin sulfate proteoglycans (CSPGs), and proteins in the Golgi apparatus is dramatically reduced by low concentrations of BFA in which Golgi morphology is unaffected and secretion still takes place. BFA treatment seems to reduce sulfation by inhibition of the uptake of adenosine 3'-phosphate 5'-phosphosulfate (PAPS) into the Golgi lumen, and the inhibitory effect of BFA was similar for HSPGs, CSPGs, and proteins. This was different from the effect of chlorate, a well known inhibitor of PAPS synthesis in the cytoplasm. Low concentrations of chlorate (2-5 mm) inhibited sulfation of CSPGs and proteins only, whereas higher concentrations (15-30 mm) were required to inhibit sulfation of HSPGs. Golgi fractions pretreated with BFA had a reduced capacity for the synthesis of glycosaminoglycans (GAGs), but control level capacity could be restored by the addition of cytosol from various sources. This indicates that the PAPS pathway to the Golgi lumen depends on a BFA-sensitive factor that is present both on Golgi membranes and in the cytoplasm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brefeldin A / pharmacology*
  • Cell Line
  • Chondroitin ABC Lyase / pharmacology
  • Chondroitin Sulfate Proteoglycans / metabolism
  • Chromatography, Gel
  • Chromatography, Ion Exchange
  • Cytoplasm / metabolism*
  • Cytosol / metabolism
  • Dogs
  • Dose-Response Relationship, Drug
  • Electrophoresis, Polyacrylamide Gel
  • Golgi Apparatus / drug effects*
  • Golgi Apparatus / metabolism*
  • Heparan Sulfate Proteoglycans / metabolism
  • Heparitin Sulfate / biosynthesis
  • Phosphoadenosine Phosphosulfate / metabolism
  • Protein Synthesis Inhibitors / pharmacology*
  • Sodium Hydroxide / pharmacology
  • Subcellular Fractions / metabolism

Substances

  • Chondroitin Sulfate Proteoglycans
  • Heparan Sulfate Proteoglycans
  • Protein Synthesis Inhibitors
  • Brefeldin A
  • Phosphoadenosine Phosphosulfate
  • Sodium Hydroxide
  • Heparitin Sulfate
  • Chondroitin ABC Lyase