Defective N-sulfation of heparan sulfate proteoglycans limits PDGF-BB binding and pericyte recruitment in vascular development.

نویسندگان

  • Alexandra Abramsson
  • Sindhulakshmi Kurup
  • Marta Busse
  • Shuhei Yamada
  • Per Lindblom
  • Edith Schallmeiner
  • Denise Stenzel
  • Dominique Sauvaget
  • Johan Ledin
  • Maria Ringvall
  • Ulf Landegren
  • Lena Kjellén
  • Göran Bondjers
  • Jin-ping Li
  • Ulf Lindahl
  • Dorothe Spillmann
  • Christer Betsholtz
  • Holger Gerhardt
چکیده

During vascular development, endothelial platelet-derived growth factor B (PDGF-B) is critical for pericyte recruitment. Deletion of the conserved C-terminal heparin-binding motif impairs PDGF-BB retention and pericyte recruitment in vivo, suggesting a potential role for heparan sulfate (HS) in PDGF-BB function during vascular development. We studied the participation of HS chains in pericyte recruitment using two mouse models with altered HS biosynthesis. Reduction of N-sulfation due to deficiency in N-deacetylase/N-sulfotransferase-1 attenuated PDGF-BB binding in vitro, and led to pericyte detachment and delayed pericyte migration in vivo. Reduced N-sulfation also impaired PDGF-BB signaling and directed cell migration, but not proliferation. In contrast, HS from glucuronyl C5-epimerase mutants, which is extensively N- and 6-O-sulfated, but lacks 2-O-sulfated L-iduronic acid residues, retained PDGF-BB in vitro, and pericyte recruitment in vivo was only transiently delayed. These observations were supported by in vitro characterization of the structural features in HS important for PDGF-BB binding. We conclude that pericyte recruitment requires HS with sufficiently extended and appropriately spaced N-sulfated domains to retain PDGF-BB and activate PDGF receptor beta (PDGFRbeta) signaling, whereas the detailed sequence of monosaccharide and sulfate residues does not appear to be important for this interaction.

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عنوان ژورنال:
  • Genes & development

دوره 21 3  شماره 

صفحات  -

تاریخ انتشار 2007