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  4. Points regarding cell transplantation for the treatment of spinal cord injury

Points regarding cell transplantation for the treatment of spinal cord injury

Neural Regeneration Research, 2016 · DOI: 10.4103/1673-5374.187021 · Published: July 1, 2016

Spinal Cord InjuryRegenerative Medicine

Simple Explanation

Cell transplantation is being explored as a way to treat spinal cord injuries. The goal is for the transplanted cells to survive and integrate into the damaged spinal cord, providing a structure for new nerve growth. However, some cells don't survive long-term but still improve recovery. Bone marrow stromal cells (BMSCs) and choroid plexus epithelial cells (CPECs) are examples of cells that don't survive long after transplantation but still promote nerve regeneration and locomotor improvement. It's thought they release factors that help with tissue repair. Neural stem/progenitor cells (NSPCs) can survive long-term, proliferate, and differentiate, but controlling their behavior to ensure they integrate properly is challenging. Therefore, the safety of NSPCs in clinical applications is a concern.

Study Duration
Not specified
Participants
Rats and human patients in clinical trials
Evidence Level
Review of preclinical and clinical studies

Key Findings

  • 1
    BMSCs, BMNCs, and CPECs enhance axon regeneration and locomotor function without long-term survival in the host spinal cord, suggesting the release of trophic factors.
  • 2
    Schwann cells survive long-term and act as a scaffold for regenerating axons, overcoming the glial scar barrier, making them clinically relevant.
  • 3
    NSPCs, while capable of long-term survival, proliferation, and differentiation, pose safety concerns due to difficulties in controlling their behavior and may not consistently improve locomotor function.

Research Summary

Transplantation of somatic cells like BMSCs, BMNCs, and CPECs enhances axon regeneration and locomotor improvements, despite their short-term survival and lack of integration into the host spinal cord. Schwann cells, in contrast, survive long-term and are integrated into the host spinal cord, acting as a scaffold for regenerating axons and overcoming the glial scar. NSPCs survive long-term, proliferate, and differentiate but raise safety concerns due to the difficulty in controlling their behavior, and their effect on locomotor improvement is inconsistent.

Practical Implications

Clinical Application of BMSCs and BMNCs

BMSCs and BMNCs can be safely applied in clinical settings due to their short-term survival and absence of adverse effects.

Schwann Cell Therapy

Schwann cells are considered safe and effective for clinical application as they provide a scaffold for axonal regeneration.

NSPC Research

Further research is needed to develop methods to control the behavior of NSPCs before they can be safely used in clinical applications.

Study Limitations

  • 1
    Short-term survival of some transplanted cells
  • 2
    Difficulty controlling NSPC behavior
  • 3
    Potential blocking of axons by glial scar

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