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Ephrin-B3 reverse signaling through Grb4 and cytoskeletal regulators mediates axon pruning.

Nature neuroscience | Mar 24, 2009

http://www.ncbi.nlm.nih.gov/pubmed/19182796

It has been suggested that ephrin-B proteins have receptor-like roles in the control of axon pathfinding by repulsion, although it is largely unknown how the reverse signals are coupled to downstream intracellular molecules and how they induce cytoskeletal reorganization at the axon terminal. We found that ephrin-B3 (EB3) was able to function as a repulsive guidance receptor and mediate stereotyped pruning of murine hippocampal mossy fiber axons during postnatal development. Targeted intracellular point mutants showed that axon pruning requires tyrosine phosphorylation-dependent reverse signaling and coupling to the SH2/SH3 adaptor protein Grb4 (also known as Nckbeta/Nck2). Furthermore, we found that the second SH3 domain of Grb4 is required and sufficient for axon pruning/retraction by mediating interactions with Dock180 and PAK to bring about guanine nucleotide exchange and signaling downstream of Rac, respectively. Our results reveal a previously unknown pathway that controls axon pruning and elucidate the biochemical mechanism by which ephrin-B reverse signals regulate actin dynamics to bring about the retraction of growth cones.

Pubmed ID: 19182796 RIS Download

Mesh terms: Actins | Adaptor Proteins, Signal Transducing | Animals | Axons | COS Cells | Cells, Cultured | Cercopithecus aethiops | Coculture Techniques | Cytoskeletal Proteins | Ephrin-B3 | Gene Knock-In Techniques | Growth Cones | Mice | Mice, Knockout | Mice, Transgenic | Mossy Fibers, Hippocampal | Oncogene Proteins | Signal Transduction | Transduction, Genetic

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Associated grants

  • Agency: NEI NIH HHS, Id: R01 EY017434
  • Agency: NEI NIH HHS, Id: R01 EY017434
  • Agency: NEI NIH HHS, Id: R01 EY017434-04
  • Agency: NIMH NIH HHS, Id: R01 MH066332
  • Agency: NIMH NIH HHS, Id: R01 MH066332
  • Agency: NIMH NIH HHS, Id: R01 MH066332-06A2

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