Corticospinal tract fibers cross the ephrin-B3-negative part of the midline of the spinal cord after brain injury

Neurosci Res. 2011 Mar;69(3):187-95. doi: 10.1016/j.neures.2010.12.004. Epub 2010 Dec 13.

Abstract

The fibers of corticospinal tract (CST), which control fine motor function, predominantly project to the contralateral spinal cord, not recross to the ipsilateral side. Ephrin-B3, which is expressed in the midline of the spinal cord, and its receptor, EphA4, are crucial for preventing CST fibers from recrossing the midline in the developing spinal cord. However, these fibers can cross the midline to the denervated side after a unilateral CST or cortical injury. We determined the reason CST fibers can cross the midline after a cortical injury and the changes in ephrin-B3-EphA4 signaling associated with such a crossing. We first examined axonal sprouting from CST fibers after unilateral ablation of the motor cortex in postnatal and adult mice. CST fibers crossed the midline of the spinal cord after cortical ablation, especially when conducted during the early postnatal period. These fibers were well associated with functional recovery after the injury. We next assessed the mRNA expression of ephrin-B3 and EphA4 before and after the ablation. Surprisingly, no changes were detected in the expression patterns. We found, however, that ephrin-B3 expression in the ventral part of the midline disappeared after postnatal day 9 (P9), but was pronounced along the entire midline before P6. Most of the CST fibers crossed the midline through the ventral region, where ephrin-B3 expression was absent. Our results suggest that ephrin-B3 is not expressed along the entire midline of the spinal cord, and sprouting axons can cross the midline at ephrin-B3-negative areas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Animals, Newborn
  • Biotin / analogs & derivatives
  • Biotin / metabolism
  • Brain Injuries / pathology*
  • Brain Injuries / physiopathology
  • Dextrans / metabolism
  • Ephrin-B3 / metabolism*
  • Functional Laterality
  • Locomotion / physiology
  • Mice
  • Mice, Inbred C57BL
  • Nerve Fibers / pathology
  • Nerve Fibers / physiology*
  • Protein Kinase C / metabolism
  • Pyramidal Tracts / growth & development
  • Pyramidal Tracts / metabolism
  • Pyramidal Tracts / pathology*
  • Receptor, EphA4 / metabolism
  • Recovery of Function / physiology
  • Spinal Cord / growth & development
  • Spinal Cord / metabolism*
  • Spinal Cord / pathology

Substances

  • Dextrans
  • Ephrin-B3
  • biotinylated dextran amine
  • Biotin
  • protein kinase C gamma
  • Receptor, EphA4
  • Protein Kinase C