Rerouting of fibroblast growth factor 2 to the classical secretory pathway results in post-translational modifications that block binding to heparan sulfate proteoglycans

FEBS Lett. 2008 Jul 9;582(16):2387-92. doi: 10.1016/j.febslet.2008.05.042. Epub 2008 Jun 5.

Abstract

FGF-2 is a proangiogenic growth factor secreted by unconventional means. It is unknown why FGF-2 takes an ER/Golgi-independent secretory route. We find that secretion of FGF-2 via the ER/Golgi system causes post-translational modifications that prevent binding to heparan sulfate proteoglycans (HSPGs), an interaction that is critically important for both FGF-2 storage and signal transduction. This loss of function is due to artificial O-glycosylation mainly resulting in the addition of glycosaminoglycan chains of the chrondroitin sulfate type. Our findings suggest that the unconventional mechanism of FGF-2 export is an ancient pathway of protein secretion that, in the course of evolution, has been kept due to the inability of the classical secretory pathway to export FGF-2 in a functional form.

MeSH terms

  • Animals
  • CHO Cells
  • Chondroitin Sulfates / metabolism
  • Cricetinae
  • Cricetulus
  • Endoplasmic Reticulum / metabolism
  • Fibroblast Growth Factor 2 / chemistry
  • Fibroblast Growth Factor 2 / metabolism*
  • Glycosylation
  • Golgi Apparatus / metabolism
  • Heparan Sulfate Proteoglycans / metabolism*
  • Heparin / metabolism
  • Protein Binding
  • Protein Processing, Post-Translational*
  • Protein Sorting Signals

Substances

  • Heparan Sulfate Proteoglycans
  • Protein Sorting Signals
  • chondroitin sulfate glycosaminoglycan
  • Fibroblast Growth Factor 2
  • Heparin
  • Chondroitin Sulfates