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  4. Comparison of Cellular Architecture, Axonal Growth, and Blood Vessel Formation Through Cell-Loaded Polymer Scaffolds in the Transected Rat Spinal Cord

Comparison of Cellular Architecture, Axonal Growth, and Blood Vessel Formation Through Cell-Loaded Polymer Scaffolds in the Transected Rat Spinal Cord

TISSUE ENGINEERING: Part A, 2014 · DOI: 10.1089/ten.tea.2013.0551 · Published: August 8, 2014

Spinal Cord InjuryRegenerative MedicineBiomedical

Simple Explanation

This study investigates the use of polymer scaffolds loaded with different cell types to promote regeneration after spinal cord injury in rats. The scaffolds were implanted after a complete spinal cord transection, and the effects of Schwann cells and mesenchymal stem cells (MSCs) on tissue regeneration, axonal growth, and blood vessel formation were compared. The researchers examined how each scaffold type influenced the architecture of the regenerated tissue, focusing on astrocytosis (scarring), axon regeneration, and blood vessel growth. They used immunohistochemistry and stereology to analyze the cellular composition and structure within the scaffolds. The study found that Schwann cells augmented axon regeneration, while MSCs did not support axon growth. Additionally, Schwann cells led to the formation of high numbers of small, densely packed blood vessels, while MSCs resulted in fewer, larger vessels. These differences in blood vessel morphology correlated with axonal regeneration, suggesting the importance of blood flow rate and vessel density.

Study Duration
4 weeks
Participants
Female SD rats weighing 230–250 g
Evidence Level
Not specified

Key Findings

  • 1
    Axon regeneration was significantly augmented by Schwann cell implantation, while eGFP-MSCs did not support axon growth in the transected spinal cord.
  • 2
    Schwann cell scaffolds had high numbers of small, densely packed blood vessels, while eGFP-MSC scaffolds contained fewer, larger vessels.
  • 3
    There was a positive linear correlation between axon counts and vessel length density, surface density, and volume fraction; increased axon number also correlated with decreasing vessel diameter.

Research Summary

This study used multichannel polymer scaffolds in a complete spinal cord transection injury model in rats to compare the effects of Schwann cells and mesenchymal stem cells (MSCs) on tissue regeneration. The researchers found that Schwann cells augmented axonal regeneration and promoted the formation of small, densely packed blood vessels, while MSCs did not support axonal growth and led to the formation of fewer, larger vessels. The study demonstrated a positive correlation between axon counts and vessel density, as well as an inverse correlation between axon counts and vessel diameter, highlighting the importance of blood flow rate and vessel morphology in supporting axonal regeneration.

Practical Implications

Scaffold Design

The study suggests that scaffolds designed to promote the formation of high numbers of small blood vessels may be more effective in supporting axonal regeneration after spinal cord injury.

Cellular Therapies

Schwann cell implantation may be a more effective cellular therapy for promoting axonal regeneration compared to MSCs in the context of spinal cord injury.

Microenvironment Engineering

Engineering the microenvironment within the scaffold to influence vascularity and blood flow rate could be a key strategy for enhancing axonal regeneration.

Study Limitations

  • 1
    Postoperative animal mortality varied between groups.
  • 2
    No significant functional recovery of motor function was observed.
  • 3
    Low survival rate of transplanted cells.

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