IGF-I specifically enhances axon outgrowth of corticospinal motor neurons

Nat Neurosci. 2006 Nov;9(11):1371-81. doi: 10.1038/nn1789. Epub 2006 Oct 22.


Corticospinal motor neurons (CSMN) are among the most complex CNS neurons; they control voluntary motor function and are prototypical projection neurons. In amyotrophic lateral sclerosis (ALS), both spinal motor neurons and CSMN degenerate; their damage contributes centrally to the loss of motor function in spinal cord injury. Direct investigation of CSMN is severely limited by inaccessibility in the heterogeneous cortex. Here, using new CSMN purification and culture approaches, and in vivo analyses, we report that insulin-like growth factor-1 (IGF-I) specifically enhances the extent and rate of murine CSMN axon outgrowth, mediated via the IGF-I receptor and downstream signaling pathways; this is distinct from IGF-I support of neuronal survival. In contrast, brain-derived neurotrophic factor (BDNF) enhances branching and arborization, but not axon outgrowth. These experiments define specific controls over directed differentiation of CSMN, indicate a distinct role of IGF-I in CSMN axon outgrowth during development, and might enable control over CSMN derived from neural precursors.

Publication types

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

MeSH terms

  • Animals
  • Axons / physiology*
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Cell Proliferation / drug effects
  • Cell Separation
  • Cell Size
  • Cell Survival / physiology
  • Flow Cytometry
  • Insulin-Like Growth Factor I / physiology*
  • Mice
  • Motor Neurons / physiology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Pyramidal Tracts / cytology
  • Pyramidal Tracts / physiology*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology


  • Brain-Derived Neurotrophic Factor
  • Insulin-Like Growth Factor I
  • Phosphatidylinositol 3-Kinases