European Journal of Neuroscience · 2004 · 137 citations · 12 references
MedicineNeurobiologyNeuroscienceNeuroanatomyNeuroimmunologyRegenerative MedicineAxonal SproutingCentral Nervous SystemNerve RegenerationNervous TissueNeural RegenerationSpinal Cord InjuryAxon RegenerationCentral Nervous System RepairCompensatory SproutingCorticospinal Tract RegenerationCorticospinal Tract SproutingSpinal Cord Injury RepairSpinal Cord RegenerationSprouting After Spinal Cord Injury
Neutralizing the myelin-associated growth inhibitor Nogo-A in adult spinal cord-injured rats can promote regeneration of injured and compensatory sprouting of uninjured axons. Nogo-A is present in humans, making its neutralization a possible novel treatment option for paraplegic patients. In this study we examined the effects of an extensively used anti-Nogo-A antibody (mAb IN-1) on the regenerative capabilities of lesioned corticospinal tract (CST) axons in a primate, the Marmoset monkey. Unilateral thoracic lesions of the CST were performed in six adult Marmosets, followed by the application of mAb IN-1 into the cerebrospinal fluid circulation by a graft of hybridoma cells. A unilateral injection of biotin dextran amine into the motor cortex was performed to analyse sprouting and regeneration of the lesioned axons. In the control antibody-treated animal CST fibers stopped rostral to the lesion site and often showed retraction bulbs. In contrast, in four out of five mAb IN-1-treated animals fine labeled neurites had grown into, through and around the lesion site. Thus, this study provides first anatomical evidence that in primates, the neutralization of the myelin-associated inhibitor Nogo-A results in increased regenerative sprouting and growth of lesioned spinal cord axons.
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Regenerating the damaged central nervous system
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Medicine, Neurobiology, Neuroscience +12
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