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Decorin promotes robust axon growth on inhibitory CSPGs and myelin via a direct effect on neurons.

Abstract
Inhibitory chondroitin sulfate proteoglycans (CSPGs) and myelin-associated molecules are major impediments to axon regeneration within the adult central nervous system (CNS). Decorin infusion can however suppress the levels of multiple inhibitory CSPGs and promote axon growth across spinal cord injuries [Davies, J.E., Tang, X., Denning, J.W., Archibald, S.J., and Davies, S.J., 2004. Decorin suppresses neurocan, brevican, phosphacan and NG2 expression and promotes axon growth across adult rat spinal cord injuries. Eur. J. Neurosci. 19, 1226-1242]. A question remained as to whether decorin can also increase axon growth on inhibitory CSPGs and myelin via a direct effect on neurons. We have therefore conducted an in vitro analysis of neurite extension by decorin-treated adult dorsal root ganglion (DRG) neurons cultured on substrates of inhibitory CSPGs or myelin membranes mixed with laminin. Decorin treatment promoted 14.5 and 5-fold increases in average neurite length/neuron over untreated controls on CSPGs or myelin membranes respectively. In addition to suppressing inhibitory scar formation, our present data shows that decorin can directly boost the ability of neurons to extend axons within CSPG or myelin rich environments.
AuthorsKenneth Minor, Xiufeng Tang, Genevieve Kahrilas, Simon J Archibald, Jeannette E Davies, Stephen J Davies
JournalNeurobiology of disease (Neurobiol Dis) Vol. 32 Issue 1 Pg. 88-95 (Oct 2008) ISSN: 1095-953X [Electronic] United States
PMID18638554 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Chondroitin Sulfate Proteoglycans
  • DCN protein, human
  • Dcn protein, rat
  • Decorin
  • Extracellular Matrix Proteins
  • Proteoglycans
Topics
  • Animals
  • Axons (physiology)
  • Cells, Cultured
  • Chondroitin Sulfate Proteoglycans (physiology)
  • Decorin
  • Extracellular Matrix Proteins (physiology)
  • Humans
  • Myelin Sheath (physiology)
  • Neurites (physiology)
  • Neurons (physiology)
  • Proteoglycans (physiology)
  • Rats
  • Rats, Sprague-Dawley

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