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

Nan Jie Xu, Mark Henkemeyer

Research output: Contribution to journalArticle

99 Citations (Scopus)

Abstract

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 Nckβ/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.

Original languageEnglish (US)
Pages (from-to)268-276
Number of pages9
JournalNature Neuroscience
Volume12
Issue number3
DOIs
StatePublished - Mar 2009

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Ephrin-B3
Neuronal Plasticity
Ephrins
Hippocampal Mossy Fibers
Growth Cones
Guanine Nucleotides
src Homology Domains
Presynaptic Terminals
Axons
Tyrosine
Actins
Phosphorylation
Proteins

ASJC Scopus subject areas

  • Neuroscience(all)

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Ephrin-B3 reverse signaling through Grb4 and cytoskeletal regulators mediates axon pruning. / Xu, Nan Jie; Henkemeyer, Mark.

In: Nature Neuroscience, Vol. 12, No. 3, 03.2009, p. 268-276.

Research output: Contribution to journalArticle

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