Spontaneous regeneration of cholecystokinergic reticulospinal axons after a complete spinal cord injury in sea lampreys.

Comput Struct Biotechnol J

Department of Functional Biology, CIBUS, Faculty of Biology, Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain.

Published: December 2024

AI Article Synopsis

  • Lampreys can naturally regain their swimming ability after a complete spinal cord injury (SCI) due to the regeneration of their descending axons, a process that hasn’t been thoroughly studied in smaller axon populations often found in mammals.
  • Research focused on cholecystokinin (CCK), a neuropeptide that influences several functions, has shown that in larval lampreys, CCKergic axons can partially regenerate, recovering about 81% of the original axonal profiles within 10 weeks post-injury.
  • The study found that improved swimming performance in injured lampreys correlates with the resurgence of CCKergic axons, suggesting these neuropeptidergic systems play a significant role in recovery of locom

Article Abstract

In contrast to humans, lampreys spontaneously recover their swimming capacity after a complete spinal cord injury (SCI). This recovery process involves the regeneration of descending axons. Spontaneous axon regeneration in lampreys has been mainly studied in giant descending neurons. However, the regeneration of neurochemically distinct descending neuronal populations with small-caliber axons, as those found in mammals, has been less studied. Cholecystokinin (CCK) is a regulatory neuropeptide found in the brain and spinal cord that modulates several processes such as satiety, or locomotion. CCK shows high evolutionary conservation and is present in all vertebrate species. Work in lampreys has shown that all CCKergic spinal cord axons originate in a single neuronal population located in the caudal rhombencephalon. Here, we investigate the spontaneous regeneration of CCKergic descending axons in larval lampreys following a complete SCI. Using anti-CCK-8 immunofluorescence, confocal microscopy and lightning adaptive deconvolution, we demonstrate the partial regeneration of CCKergic axons (81% of the number of axonal profiles seen in controls) 10 weeks after the injury. Our data also revealed a preference for regeneration of CCKergic axons in lateral spinal cord regions. Regenerated CCKergic axons exhibit colocalization with synaptic vesicle marker SV2, indicative of functional synaptic connections. We also extracted swimming dynamics in injured animals by using DeepLabCut. Interestingly, the degree of CCKergic reinnervation correlated with improved swimming performance in injured animals, suggesting a potential role in locomotor recovery. These findings open avenues for further exploration into the role of specific neuropeptidergic systems in post-SCI spinal locomotor networks.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10776906PMC
http://dx.doi.org/10.1016/j.csbj.2023.12.014DOI Listing

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