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p75(NTR) mediates ephrin-A reverse signaling required for axon repulsion and mapping.

Reverse signaling by ephrin-As upon binding EphAs controls axon guidance and mapping. Ephrin-As are GPI-anchored to the membrane, requiring that they complex with transmembrane proteins that transduce their signals. We show that the p75 neurotrophin receptor (NTR) serves this role in retinal axons. p75(NTR) and ephrin-A colocalize within caveolae along retinal axons and form a complex required for Fyn phosphorylation upon binding EphAs, activating a signaling pathway leading to cytoskeletal changes. In vitro, retinal axon repulsion to EphAs by ephrin-A reverse signaling requires p75(NTR), but repulsion to ephrin-As by EphA forward signaling does not. Constitutive and retina-specific p75(NTR) knockout mice have aberrant anterior shifts in retinal axon terminations in superior colliculus, consistent with diminished repellent activity mediated by graded ephrin-A reverse signaling induced by graded collicular EphAs. We conclude that p75(NTR) is a signaling partner for ephrin-As and the ephrin-A- p75(NTR) complex reverse signals to mediate axon repulsion required for guidance and mapping.

Pubmed ID: 18786358


  • Lim YS
  • McLaughlin T
  • Sung TC
  • Santiago A
  • Lee KF
  • O'Leary DD



Publication Data

September 11, 2008

Associated Grants

  • Agency: NEI NIH HHS, Id: R01 EY 07025
  • Agency: NEI NIH HHS, Id: R01 EY007025
  • Agency: NEI NIH HHS, Id: R01 EY007025-24
  • Agency: NICHD NIH HHS, Id: R01 HD034534
  • Agency: NICHD NIH HHS, Id: R01 HD034534-11
  • Agency: NICHD NIH HHS, Id: R01 HD034534-12
  • Agency: NINDS NIH HHS, Id: R01 NS060833
  • Agency: NINDS NIH HHS, Id: R01 NS060833-01A1
  • Agency: NINDS NIH HHS, Id: R01 NS060833-02
  • Agency: NINDS NIH HHS, Id: R01 NS060833-02S1

Mesh Terms

  • Amino Acids
  • Animals
  • Animals, Newborn
  • Axons
  • Brain Mapping
  • Cell Line, Transformed
  • Ephrins
  • GAP-43 Protein
  • Gene Expression Regulation
  • Green Fluorescent Proteins
  • Humans
  • Mice
  • Mice, Transgenic
  • Mutation
  • Nerve Tissue Proteins
  • Proto-Oncogene Proteins c-fyn
  • Rats
  • Receptors, Nerve Growth Factor
  • Retina
  • Retinal Ganglion Cells
  • Signal Transduction
  • Visual Pathways