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  4. Long-term survival, axonal growth-promotion, and myelination of Schwann cells grafted into contused spinal cord in adult rats

Long-term survival, axonal growth-promotion, and myelination of Schwann cells grafted into contused spinal cord in adult rats

Exp Neurol, 2014 · DOI: 10.1016/j.expneurol.2014.05.022 · Published: November 1, 2014

Spinal Cord InjuryRegenerative MedicineNeurology

Simple Explanation

This study explores the potential of Schwann cells (SCs) transplantation to treat spinal cord injury (SCI) in rats. SCs were genetically modified to express green fluorescent protein (GFP), allowing them to be easily tracked after transplantation. The study found that transplanted SCs survived remarkably well for up to 24 weeks after grafting into the injured spinal cord. They were able to proliferate, migrate along the central canal, and myelinate regenerated axons. Although the transplanted SCs showed promising survival and functionality, they did not result in significant behavioral improvements in the rats. This suggests that a combination of strategies may be needed to achieve meaningful functional regeneration after SCI.

Study Duration
24 Weeks
Participants
56 Sprague Dawley adult rats
Evidence Level
Not specified

Key Findings

  • 1
    Grafted SCs-GFP exhibited remarkable survival up to 24 weeks post-grafting in the contused spinal cord of adult rats.
  • 2
    SCs-GFP proliferated after injection, peaking at 2 weeks, and then gradually decreasing thereafter, ceasing by 12 weeks post-grafting.
  • 3
    Grafted SCs-GFP migrated along the central canal and myelinated regenerated axons within the lesion site, expressing P0 and MBP.

Research Summary

This study investigated the long-term survival, axonal growth-promotion, and myelination potential of Schwann cells (SCs) grafted into a contused spinal cord in adult rats. The key findings revealed remarkable survival of grafted SCs-GFP up to 24 weeks post-grafting, proliferation peaking at 2 weeks, and migration along the central canal, as well as myelination of regenerated axons within the lesion site. Despite the promising survival and functionality of the transplanted SCs, significant behavioral improvements were not observed, suggesting that combinatorial strategies are essential for meaningful functional regeneration after SCI.

Practical Implications

Therapeutic Potential

SCs have the potential to be used in cell-based therapies for spinal cord injuries.

Combined Strategies

Combining SC transplantation with other strategies may be needed for significant functional recovery.

Immunosuppression

Consistent immunosuppression is needed for long-term survival of grafted SCs.

Study Limitations

  • 1
    Lack of substantial behavioral recovery after SCs-GFP transplantation.
  • 2
    Limited migration of SCs-GFP within the injured spinal cord.
  • 3
    Possible immune response to grafted cells.

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