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Chronic neuronal activation increases dynamic microtubules to enhance functional axon regeneration after dorsal root crush injury. | LitMetric

AI Article Synopsis

  • Dorsal root crush injuries prevent sensory axons from regenerating into the spinal cord, but activating dorsal root ganglion (DRG) neurons can enhance this growth in lab models.
  • * In vivo experiments show that daily chemogenetic activation of DRG neurons for 12 weeks helps regenerate axons across damaged areas, leading to functional recovery in movement tasks.
  • * The increase in axon growth is linked to changes in tubulin modifications, which suggest a mechanism for stimulating axon extension in response to neuronal activation.

Article Abstract

After a dorsal root crush injury, centrally-projecting sensory axons fail to regenerate across the dorsal root entry zone (DREZ) to extend into the spinal cord. We find that chemogenetic activation of adult dorsal root ganglion (DRG) neurons improves axon growth on an in vitro model of the inhibitory environment after injury. Moreover, repeated bouts of daily chemogenetic activation of adult DRG neurons for 12 weeks post-crush in vivo enhances axon regeneration across a chondroitinase-digested DREZ into spinal gray matter, where the regenerating axons form functional synapses and mediate behavioral recovery in a sensorimotor task. Neuronal activation-mediated axon extension is dependent upon changes in the status of tubulin post-translational modifications indicative of highly dynamic microtubules (as opposed to stable microtubules) within the distal axon, illuminating a novel mechanism underlying stimulation-mediated axon growth. We have identified an effective combinatory strategy to promote functionally-relevant axon regeneration of adult neurons into the CNS after injury.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705672PMC
http://dx.doi.org/10.1038/s41467-020-19914-3DOI Listing

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