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  4. Transplantation of canine olfactory ensheathing cells producing chondroitinase ABC promotes chondroitin sulphate proteoglycan digestion and axonal sprouting following spinal cord injury

Transplantation of canine olfactory ensheathing cells producing chondroitinase ABC promotes chondroitin sulphate proteoglycan digestion and axonal sprouting following spinal cord injury

PLoS ONE, 2017 · DOI: https://doi.org/10.1371/journal.pone.0188967 · Published: December 11, 2017

Spinal Cord InjuryRegenerative MedicineNeurology

Simple Explanation

This study explores a novel approach to spinal cord injury (SCI) treatment by transplanting genetically modified canine olfactory ensheathing cells (OECs) into rats with SCI. These OECs are engineered to produce chondroitinase ABC, an enzyme that breaks down substances inhibiting nerve repair. The modified OECs effectively digested the inhibitory substances at the injury site, leading to increased nerve fiber sprouting and regeneration. This suggests a potential strategy for promoting neural repair after SCI. The combination of cell transplantation and enzyme delivery may offer a promising therapeutic avenue for SCI, potentially applicable to both veterinary and human medicine.

Study Duration
4 weeks
Participants
12 adult 250g male athymic nude rats
Evidence Level
Not specified

Key Findings

  • 1
    Genetically modified canine OECs survived transplantation into rat spinal cord lesions for at least four weeks.
  • 2
    The transplanted OECs effectively digested chondroitin sulphate proteoglycans (CSPGs) at the site of injury, as evidenced by C4S labeling.
  • 3
    There was an increase in axonal sprouting within the corticospinal tract rostral to the lesion and an increase in the number of corticospinal axons caudal to the lesion, suggestive of axonal regeneration.

Research Summary

This study investigated the transplantation of canine olfactory ensheathing cells (OECs) genetically modified to produce chondroitinase ABC (ChABC) into a rodent model of spinal cord injury (SCI). The results demonstrated that these ChABC-producing canine OECs survived at the lesion site, effectively digested chondroitin sulphate proteoglycans, and promoted axonal sprouting and regeneration. The findings suggest that the combination of OEC transplantation and ChABC delivery is a potential strategy for promoting neural regeneration following SCI.

Practical Implications

Therapeutic Strategy

The combination of OEC transplantation and chondroitinase ABC delivery shows promise as a therapeutic strategy for spinal cord injury.

Clinical Translation

The use of canine OECs provides a translational bridge between experimental rodent models and human clinical trials.

Veterinary Applications

This approach has potential applications in veterinary practice for treating spinal cord injuries in companion animals.

Study Limitations

  • 1
    Poor cell survival rate of transplanted cells.
  • 2
    Potential immune rejection of xenotransplanted cells.
  • 3
    Study was conducted in an acute injury model; long-term effects need to be evaluated.

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