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  4. Rat vibrissa dermal papilla cells promote healing of spinal cord injury following transplantation

Rat vibrissa dermal papilla cells promote healing of spinal cord injury following transplantation

EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2018 · DOI: 10.3892/etm.2018.5916 · Published: January 18, 2018

Spinal Cord InjuryRegenerative Medicine

Simple Explanation

This study investigates the potential of dermal papilla cells (DPCs) as an alternative to bone marrow mesenchymal stem cells (BMSCs) for treating spinal cord injuries (SCIs). DPCs and BMSCs were taken from rats and transplanted into spinal cord lesion sites. The researchers compared the survival and therapeutic effects of DPC grafts versus BMSC grafts in rats with completely transected spinal cords. They used in vivo imaging and histochemical examinations to assess lesion filling, cell survival, axon formation, and blood vessel development. The study found that DPC grafts showed enhanced lesion filling and survival compared to BMSC grafts. Additionally, more axons and blood vessel-like structures formed within the lesion sites in the DPC transplant group.

Study Duration
Not specified
Participants
27 adult female SD rats and 3 adult male green fluorescence protein (GFP)‑transgenic SD rats
Evidence Level
Not specified

Key Findings

  • 1
    DPC grafts exhibited enhanced lesion filling and survival compared with BMSC grafts on days 14 and 21 post‑transplantation.
  • 2
    More axons formed within the lesion sites in the DPC transplant group, indicating that DPCs may promote axonal growth in the host.
  • 3
    CD31‑positive vessel‑like structures were more abundant in lesion sites near the grafted cells in the DPC group, suggesting that DPCs promote revascularization.

Research Summary

This study compared the therapeutic efficacy of dermal papilla cells (DPCs) and bone marrow mesenchymal stem cells (BMSCs) in repairing spinal cord injuries (SCIs) in a rat model. The results demonstrated that DPC grafts showed enhanced lesion filling and survival compared to BMSC grafts, along with increased axon formation and vascular regeneration within the lesion sites. The findings suggest that DPCs may be a valuable alternative source of stem cells for autologous cell therapy in treating SCIs, owing to their ability to promote tissue repair and regeneration.

Practical Implications

Alternative Stem Cell Source

DPCs may serve as a less invasive and more readily available autologous stem cell source for SCI treatment compared to BMSCs.

Enhanced Tissue Repair

DPC transplantation promotes greater tissue repair in SCI, including neurite outgrowth and revascularization.

Clinical Translation Potential

The study supports further investigation into the clinical application of DPCs for autologous cell therapy in SCI patients.

Study Limitations

  • 1
    The short observation period may not have been sufficient to observe complete axonal development and functional recovery.
  • 2
    The study focused on a complete transection SCI model, which may not fully represent the heterogeneity of human SCI.
  • 3
    The mechanisms by which DPCs regulate macrophage polarization require further investigation.

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