Suppression of Rho-kinase activity promotes axonal growth on inhibitory CNS substrates

Jaimie F. Borisoff, Carmen C.M. Chan, Gordon W. Hiebert, Loren Oschipok, George S. Robertson, R. Zamboni, John D. Steeves, Wolfram Tetzlaff

Résultat de recherche: Articleexamen par les pairs

198 Citations (Scopus)

Résumé

Several molecules inhibit axonal growth cones and may account for the failure of central nervous system regeneration, including myelin proteins and various chondroitan sulfate proteoglycans expressed at the site of injury. Axonal growth inhibition by myelin and chondroitan sulfate proteoglycans may in part be controlled by Rho-GTPase, which mediates growth cone collapse. Here, we tested in vitro whether pharmacological inhibition of a major downstream effector of Rho, Rho-kinase, promotes axonal outgrowth from dorsal root ganglia grown on aggrecan. Aggrecan substrates stimulated Rho activity and were inhibitory to axonal growth. Y-27632 treatment promoted the growth of axons by 5- to 10-fold and induced "steamlined" growth cones with longer filopodia and smaller lamellipodia. Interestingly, more actin bundles reminiscent of stress fibers in the central domain of the growth cone were observed when grown on aggrecan compared to laminin. In addition, Y-27632 significantly promoted axonal growth on both myelin and adult rat spinal cord cryosections. Our data suggest that suppression of Rho-kinase activity may enhance axonal regeneration in the central nervous system.

Langue d'origineEnglish
Pages (de-à)405-416
Nombre de pages12
JournalMolecular and Cellular Neurosciences
Volume22
Numéro de publication3
DOI
Statut de publicationPublished - mars 1 2003
Publié à l'externeOui

Note bibliographique

Funding Information:
This research was funded by a grant from the British Columbia Neurotrauma Fund. J.F.B., C.C.M.C., and L.O. were funded by studentships provided by the BCNTF and CIHR. W.T. holds the Rick Hansen Man in Motion Chair in Spinal Cord Research. The authors thank Drs. Timothy P. O’Connor and Matt S. Ramer for critical reading of the manuscript.

ASJC Scopus Subject Areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience
  • Cell Biology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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