• Media type: E-Article
  • Title: Control of cell shape, neurite outgrowth, and migration by a Nogo-A/HSPG iInteraction
  • Contributor: Kempf, Anissa [VerfasserIn]; Boda, Enrica [VerfasserIn]; Tews, Björn [VerfasserIn]
  • imprint: 21 September 2017
  • Published in: Developmental cell ; 43(2017), 1, Seite 24-34
  • Language: English
  • DOI: 10.1016/j.devcel.2017.08.014
  • ISSN: 1878-1551
  • Identifier:
  • Keywords: adhesion ; HSPG ; migration ; neuroblast ; nogo-A ; outgrowth ; RMS ; spreading ; SVZ ; syndecan
  • Origination:
  • Footnote:
  • Description: Summary Heparan sulfate proteoglycans (HSPGs) critically modulate adhesion-, growth-, and migration-related processes. Here, we show that the transmembrane protein, Nogo-A, inhibits neurite outgrowth and cell spreading in neurons and Nogo-A-responsive cell lines via HSPGs. The extracellular, active 180 amino acid Nogo-A region, named Nogo-A-Δ20, binds to heparin and brain-derived heparan sulfate glycosaminoglycans (GAGs) but not to the closely related chondroitin sulfate GAGs. HSPGs are required for Nogo-A-Δ20-induced inhibition of adhesion, cell spreading, and neurite outgrowth, as well as for RhoA activation. Surprisingly, we show that Nogo-A-Δ20 can act via HSPGs independently of its receptor, Sphingosine-1-Phosphate receptor 2 (S1PR2). We thereby identify the HSPG family members syndecan-3 and syndecan-4 as functional receptors for Nogo-A-Δ20. Finally, we show in explant cultures ex vivo that Nogo-A-Δ20 promotes the migration of neuroblasts via HSPGs but not S1PR2.
  • Access State: Open Access