Developmental axon pruning mediated by BDNF-p75NTR-dependent axon degeneration

Nat Neurosci. 2008 Jun;11(6):649-58. doi: 10.1038/nn.2114. Epub 2008 Apr 1.

Abstract

The mechanisms that regulate the pruning of mammalian axons are just now being elucidated. Here, we describe a mechanism by which, during developmental sympathetic axon competition, winning axons secrete brain-derived neurotrophic factor (BDNF) in an activity-dependent fashion, which binds to the p75 neurotrophin receptor (p75NTR) on losing axons to cause their degeneration and, ultimately, axon pruning. Specifically, we found that pruning of rat and mouse sympathetic axons that project to the eye requires both activity-dependent BDNF and p75NTR. p75NTR and BDNF are also essential for activity-dependent axon pruning in culture, where they mediate pruning by directly causing axon degeneration. p75NTR, which is enriched in losing axons, causes axonal degeneration by suppressing TrkA-mediated signaling that is essential for axonal maintenance. These data provide a mechanism that explains how active axons can eliminate less-active, competing axons during developmental pruning by directly promoting p75NTR-mediated axonal degeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Axons / drug effects
  • Axons / physiology*
  • Axotomy / methods
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Brain-Derived Neurotrophic Factor / physiology*
  • Cells, Cultured
  • Cholera Toxin / metabolism
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation, Developmental / drug effects
  • Gene Expression Regulation, Developmental / physiology
  • Green Fluorescent Proteins / biosynthesis
  • Green Fluorescent Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Nerve Degeneration / drug therapy
  • Nerve Degeneration / genetics
  • Nerve Degeneration / physiopathology*
  • Nerve Growth Factor / pharmacology
  • Neurons / cytology
  • Potassium Chloride / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Nerve Growth Factor / deficiency
  • Receptor, Nerve Growth Factor / physiology*
  • Stilbamidines / metabolism
  • Superior Cervical Ganglion / cytology
  • Superior Cervical Ganglion / growth & development
  • Visual Pathways / growth & development
  • Visual Pathways / metabolism

Substances

  • 2-hydroxy-4,4'-diamidinostilbene, methanesulfonate salt
  • Brain-Derived Neurotrophic Factor
  • Enzyme Inhibitors
  • Receptor, Nerve Growth Factor
  • Stilbamidines
  • Green Fluorescent Proteins
  • Potassium Chloride
  • Cholera Toxin
  • Nerve Growth Factor