Unbound MEDLINE

Spinal interneuron axons spontaneously regenerate after spinal cord injury in the adult feline. The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] Journal article

 
TitleSpinal interneuron axons spontaneously regenerate after spinal cord injury in the adult feline.
Author(s)Fenrich KK, Rose PK 
InstitutionDepartment of Physiology, Center for Neuroscience, Queen's University, Canadian Institute for Health Research Group in Sensory-Motor Integration, Kingston, Ontario, Canada. keith@biomed.queensu.ca
SourceJ Neurosci 2009 Sep 30; 29(39):12145-58.
MeSHAction Potentials
Age Factors
Animals
Axons
Cats
Cervical Vertebrae
Interneurons
Nerve Regeneration
Spinal Cord
Spinal Cord Injuries
AbstractIt is well established that long, descending axons of the adult mammalian spinal cord do not regenerate after a spinal cord injury (SCI). These axons do not regenerate because they do not mount an adequate regenerative response and growth is inhibited at the injury site by growth cone collapsing molecules, such as chondroitin sulfate proteoglycans (CSPGs). However, whether axons of axotomized spinal interneurons regenerate through the inhibitory environment of an SCI site remains unknown. Here, we show that cut axons from adult mammalian spinal interneurons can regenerate through an SCI site and form new synaptic connections in vivo. Using morphological and immunohistochemical analyses, we found that after a midsagittal transection of the adult feline spinal cord, axons of propriospinal commissural interneurons can grow across the lesion despite a close proximity of their growth cones to CSPGs. Furthermore, using immunohistochemical and electrophysiological analyses, we found that the regenerated axons conduct action potentials and form functional synaptic connections with motoneurons, thus providing new circuits that cross the transected commissures. Our results show that interneurons of the adult mammalian spinal cord are capable of spontaneous regeneration after injury and suggest that elucidating the mechanisms that allow these axons to regenerate may lead to useful new therapeutic strategies for restoring function after injury to the adult CNS.
Languageeng
Pub Type(s)Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
PubMed ID19793972
  
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