Chondroitinase ABC promotes functional recovery after spinal cord injury

The inability of axons to regenerate after a spinal cord injury in the adult mammalian central nervous system (CNS) can lead to permanent paralysis. At sites of CNS injury, a glial scar develops, containing extracellular matrix molecules including chondroitin sulphate proteoglycans (CSPGs). CSPGs are inhibitory to axon growth in vitro, and regenerating axons stop at CSPG-rich regions in vivo. Removing CSPG glycosaminoglycan (GAG) chains attenuates CSPG inhibitory activity. To test the functional effects of degrading chondroitin sulphate (CS)-GAG after spinal cord injury, we delivered chondroitinase ABC (ChABC) to the lesioned dorsal columns of adult rats. We show that intrathecal treatment with ChABC degraded CS-GAG at the injury site, upregulated a regeneration-associated protein in injured neurons, and promoted regeneration of both ascending sensory projections and descending corticospinal tract axons. ChABC treatment also restored post-synaptic activity below the lesion after electrical stimulation of corticospinal neurons, and promoted functional recovery of locomotor and proprioceptive behaviours. Our results demonstrate that CSPGs are important inhibitory molecules in vivo and suggest that their manipulation will be useful for treatment of human spinal injuries.

[1]  S. R. Thornton,et al.  Comparing Astrocytic Cell Lines that Are Inhibitory or Permissive for Axon Growth: the Major Axon-Inhibitory Proteoglycan Is NG2 , 1999, The Journal of Neuroscience.

[2]  Arnold H. Taylor NORTH–SOUTH SHIFTS OF THE GULF STREAM: OCEAN‐ATMOSPHERE INTERACTIONS IN THE NORTH ATLANTIC , 1996 .

[3]  F. Lacquaniti,et al.  Early coding of reaching in the parietooccipital cortex. , 2000, Journal of neurophysiology.

[4]  M. Schwab,et al.  Bovine CNS Myelin Contains Neurite Growth-Inhibitory Activity Associated with Chondroitin Sulfate Proteoglycans , 1999, The Journal of Neuroscience.

[5]  A. Georgopoulos,et al.  Static spatial effects in motor cortex and area 5: Quantitative relations in a two-dimensional space , 1984, Experimental Brain Research.

[6]  M. Schwab,et al.  Recovery from spinal cord injury mediated by antibodies to neurite growth inhibitors , 1995, Nature.

[7]  J. Silver,et al.  Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhibitory molecules on reactive astrocytes , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  M. Jurynec,et al.  The Chondroitin Sulfate Proteoglycans Neurocan and Phosphacan Are Expressed by Reactive Astrocytes in the Chronic CNS Glial Scar , 1999, The Journal of Neuroscience.

[9]  A B Schwartz,et al.  Motor cortical representation of speed and direction during reaching. , 1999, Journal of neurophysiology.

[10]  M. R. Droop,et al.  The nutrient status of algal cells in continuous culture , 1974, Journal of the Marine Biological Association of the United Kingdom.

[11]  J. F. Soechting,et al.  Early stages in a sensorimotor transformation , 1992, Behavioral and Brain Sciences.

[12]  A. Pouget,et al.  Efficient computation and cue integration with noisy population codes , 2001, Nature Neuroscience.

[13]  F. Lacquaniti,et al.  Representing spatial information for limb movement: role of area 5 in the monkey. , 1995, Cerebral cortex.

[14]  J. Silver,et al.  Beyond the Glial Scar: Cellular and Molecular Mechanisms by which Glial Cells Contribute to CNS Regenerative Failure , 1999 .

[15]  M S Graziano,et al.  Coding the location of the arm by sight. , 2000, Science.

[16]  J. Fawcett,et al.  Neurocan Is Upregulated in Injured Brain and in Cytokine-Treated Astrocytes , 2000, The Journal of Neuroscience.

[17]  R. Andersen,et al.  Coding of intention in the posterior parietal cortex , 1997, Nature.

[18]  M. Schwab,et al.  Neurite growth inhibitors restrict plasticity and functional recovery following corticospinal tract lesions , 1998, Nature Neuroscience.

[19]  J. Levine Increased expression of the NG2 chondroitin-sulfate proteoglycan after brain injury , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  S. McMahon,et al.  NT‐3 promotes growth of lesioned adult rat sensory axons ascending in the dorsal columns of the spinal cord , 1999, The European journal of neuroscience.

[21]  J. Verhaagen,et al.  Peripheral nerve injury fails to induce growth of lesioned ascending dorsal column axons into spinal cord scar tissue expressing the axon repellent Semaphorin3A , 2001, The European journal of neuroscience.

[22]  P. J. Radford,et al.  An 1-D vertically resolved modelling study of the ecosystem dynamics of the middle and southern Adriatic Sea , 1998 .

[23]  J. M. Colebrook,et al.  Continuous plankton records: overwintering and annual fluctuations in the abundance of zooplankton , 1985 .

[24]  L F Abbott,et al.  Transfer of coded information from sensory to motor networks , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  J. Kalaska,et al.  Deciding not to GO: neuronal correlates of response selection in a GO/NOGO task in primate premotor and parietal cortex. , 1995, Cerebral cortex.

[26]  C. Tanaka,et al.  Immunocytochemical localization of protein kinase C subspecies in the rat spinal cord: Light and electron microscopic study , 1990, The Journal of comparative neurology.

[27]  J. G. Baretta-Bekker,et al.  An improved model of carbon and nutrient dynamics in the microbial food web in marine enclosures , 1998 .

[28]  F. Lacquaniti,et al.  Short-Term Memory for Reaching to Visual Targets: Psychophysical Evidence for Body-Centered Reference Frames , 1998, The Journal of Neuroscience.

[29]  J. Fawcett,et al.  Regeneration of CNS axons back to their target following treatment of adult rat brain with chondroitinase ABC , 2001, Nature Neuroscience.

[30]  M. Tuszynski,et al.  CNS regeneration : basic science and clinical advances , 1999 .

[31]  M. Reynolds,et al.  GAP-43 expression in primary sensory neurons following central axotomy , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  H. M. Geller,et al.  An inhibitor of neurite outgrowth produced by astrocytes. , 1994, Journal of cell science.

[33]  T. Ferguson,et al.  Degradation of Chondroitin Sulfate Proteoglycan Enhances the Neurite-Promoting Potential of Spinal Cord Tissue , 1998, Experimental Neurology.

[34]  A P Batista,et al.  Reach plans in eye-centered coordinates. , 1999, Science.

[35]  H. Dai,et al.  Methods to Assess the Development and Recovery of Locomotor Function after Spinal Cord Injury in Rats , 1993, Experimental Neurology.

[36]  J. Stephens,et al.  Latitudinal Displacements of the Gulf Stream and the Abundance of Plankton in the North-East Atlantic , 1992, Journal of the Marine Biological Association of the United Kingdom.

[37]  Michael I. Jordan,et al.  Forward Models: Supervised Learning with a Distal Teacher , 1992, Cogn. Sci..

[38]  G. Plant,et al.  Inhibitory Proteoglycan Immunoreactivity Is Higher at the Caudal Than the Rostral Schwann Cell Graft-Transected Spinal Cord Interface , 2001, Molecular and Cellular Neuroscience.

[39]  G Sugihara,et al.  Distinguishing error from chaos in ecological time series. , 1990, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[40]  J. Kalaska,et al.  Parietal area 5 neuronal activity encodes movement kinematics, not movement dynamics , 2004, Experimental Brain Research.

[41]  R. An Chondroitinase ABC promotes functional recovery after spinal cord injury , 2002 .

[42]  M. Murray Strategies and mechanisms of recovery after spinal cord injury. , 1997, Advances in neurology.

[43]  J. Hurrell Decadal Trends in the North Atlantic Oscillation: Regional Temperatures and Precipitation , 1995, Science.

[44]  S. McMahon,et al.  Functional regeneration of sensory axons into the adult spinal cord , 2000, Nature.

[45]  R. Uncles,et al.  Simulating the Spring Phytoplankton Bloom in the Humber Plume, UK , 1999 .

[46]  M. Ramer,et al.  Progress in Spinal Cord Research - A refined strategy for the International Spinal Research Trust , 2000, Spinal Cord.

[47]  M. Murray,et al.  Transplantation and Gene Therapy: Combined Approaches for Repair of Spinal Cord Injury , 2001, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[48]  P. Rondot,et al.  Visuomotor ataxia. , 1977, Brain : a journal of neurology.

[49]  Michael R. Heath,et al.  Modelling the dynamics of the North Sea's Mesozooplankton , 1995 .

[50]  M. Beattie,et al.  Degeneration and Sprouting of Identified Descending Supraspinal Axons after Contusive Spinal Cord Injury in the Rat , 2001, Experimental Neurology.

[51]  D. G. George The impact of regional-scale changes in the weather on the long-term dynamics of Eudiaptomus and Daphnia in Esthwaite water, Cumbria , 2000 .

[52]  P. Strick,et al.  Input to primate motor cortex from posterior parietal cortex (area 5). II. Identification by antidromic activation , 1978, Brain Research.

[53]  V. Dietz,et al.  Improving axonal growth and functional recovery after experimental spinal cord injury by neutralizing myelin associated inhibitors , 2001, Brain Research Reviews.

[54]  S. McMahon,et al.  Keeping in touch: sensory neurone regeneration in the CNS. , 2000, Trends in pharmacological sciences.

[55]  Scott T. Grafton,et al.  Role of the posterior parietal cortex in updating reaching movements to a visual target , 1999, Nature Neuroscience.

[56]  F. Lacquaniti,et al.  Viewer-centered and body-centered frames of reference in direct visuomotor transformations , 1999, Experimental Brain Research.

[57]  P. Strick,et al.  Input to primate motor cortex from posterior parietal cortex (area 5). I. Demonstration by retrograde transport , 1978, Brain Research.

[58]  N. Shackleton,et al.  The 100,000-year ice-Age cycle identified and found to lag temperature, carbon dioxide, and orbital eccentricity , 2000, Science.

[59]  A. P. Georgopoulos,et al.  Cortical mechanisms related to the direction of two-dimensional arm movements: relations in parietal area 5 and comparison with motor cortex , 1983, Experimental Brain Research.

[60]  Gidon Eshel,et al.  Forecasting Zimbabwean maize yield using eastern equatorial Pacific sea surface temperature , 1994, Nature.

[61]  M. Tuszynski,et al.  Neurotrophic factors, cellular bridges and gene therapy for spinal cord injury , 2001, The Journal of physiology.

[62]  J. Silver,et al.  Injury-Induced Proteoglycans Inhibit the Potential for Laminin-Mediated Axon Growth on Astrocytic Scars , 1995, Experimental Neurology.

[63]  R. M. Siegel,et al.  Encoding of spatial location by posterior parietal neurons. , 1985, Science.

[64]  J. Silver,et al.  Robust Regeneration of Adult Sensory Axons in Degenerating White Matter of the Adult Rat Spinal Cord , 1999, The Journal of Neuroscience.

[65]  S. Grossberg,et al.  Cortical networks for control of voluntary arm movements under variable force conditions. , 1998, Cerebral cortex.

[66]  Franz J. Weissing,et al.  Critical depth and critical turbulence: Two different mechanisms for the development of phytoplankton blooms , 1999 .

[67]  A A Berryman,et al.  Are ecological systems chaotic - And if not, why not? , 1989, Trends in ecology & evolution.

[68]  J. Fawcett,et al.  The glial scar and central nervous system repair , 1999, Brain Research Bulletin.

[69]  P. Wall,et al.  Five sources of a dorsal root potential: their interactions and origins in the superficial dorsal horn. , 1997, Journal of neurophysiology.

[70]  S. Scott,et al.  Reaching movements with similar hand paths but different arm orientations. II. Activity of individual cells in dorsal premotor cortex and parietal area 5. , 1997, Journal of neurophysiology.

[71]  Richard A. Andersen,et al.  Coordinate transformations in the representation of spatial information , 1993, Current Opinion in Neurobiology.

[72]  D. Pandya,et al.  Projections to the frontal cortex from the posterior parietal region in the rhesus monkey , 1984, The Journal of comparative neurology.

[73]  J. Crawford,et al.  Gaze-Centered Remapping of Remembered Visual Space in an Open-Loop Pointing Task , 1998, The Journal of Neuroscience.