Brain-derived neurotrophic factor mediates non-cell-autonomous regulation of sensory neuron position and identity

J Neurosci. 2010 Oct 27;30(43):14513-21. doi: 10.1523/JNEUROSCI.4025-10.2010.

Abstract

During development, neurons migrate considerable distances to reside in locations that enable their individual functional roles. Whereas migration mechanisms have been extensively studied, much less is known about how neurons remain in their ideal locations. We sought to identify factors that maintain the position of postmigratory dorsal root ganglion neurons, neural crest derivatives for which migration and final position play an important developmental role. We found that an early developing population of sensory neurons maintains the position of later born dorsal root ganglia neurons in an activity-dependent manner. Further, inhibiting or increasing the function of brain-derived neurotrophic factor induces or prevents, respectively, migration of dorsal root ganglia neurons out of the ganglion to locations where they acquire a new identity. Overall, the results demonstrate that neurotrophins mediate non-cell-autonomous maintenance of position and thereby the identity of differentiated neurons.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Antibodies, Blocking / pharmacology
  • Brain-Derived Neurotrophic Factor / antagonists & inhibitors
  • Brain-Derived Neurotrophic Factor / physiology*
  • Cell Differentiation / physiology
  • Cell Movement / physiology
  • Dendrites / physiology
  • Ganglia, Spinal / embryology
  • Ganglia, Spinal / growth & development
  • Ganglia, Spinal / physiology
  • Immunohistochemistry
  • In Vitro Techniques
  • Microscopy, Confocal
  • Nerve Growth Factors / antagonists & inhibitors
  • Nerve Growth Factors / physiology
  • Neural Crest / physiology
  • Oligoribonucleotides, Antisense / pharmacology
  • Physical Stimulation
  • Sensory Receptor Cells / physiology*
  • Sodium Channel Blockers / pharmacology
  • Sodium Channels / drug effects
  • Sodium Channels / physiology
  • Tetrodotoxin / pharmacology
  • Zebrafish

Substances

  • Antibodies, Blocking
  • Brain-Derived Neurotrophic Factor
  • Nerve Growth Factors
  • Oligoribonucleotides, Antisense
  • Sodium Channel Blockers
  • Sodium Channels
  • Tetrodotoxin