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  4. Decellularized optic nerve functional scaffold transplant facilitates directional axon regeneration and remyelination in the injured white matter of the rat spinal cord

Decellularized optic nerve functional scaffold transplant facilitates directional axon regeneration and remyelination in the injured white matter of the rat spinal cord

NEURAL REGENERATION RESEARCH, 2021 · DOI: 10.4103/1673-5374.310696 · Published: November 1, 2021

Spinal Cord InjuryRegenerative MedicineBiomedical

Simple Explanation

This study explores a novel approach to spinal cord injury (SCI) repair using a tissue-engineered scaffold. The scaffold, made from decellularized porcine optic nerve (DON), is designed to mimic the natural environment of nerve tissue. The DON scaffold is seeded with Schwann cells that overproduce neurotrophin-3 (NT-3), a growth factor known to support nerve cell survival and regeneration. This combination aims to promote directional axon growth and remyelination in the injured spinal cord. Results showed that the DON scaffold, when transplanted into rats with SCI, facilitated the directional growth of regenerating axons, improved myelin sheath recovery, and reduced inflammation. These findings suggest that DON scaffolds may be a promising tool for SCI repair.

Study Duration
4 weeks
Participants
Adult female Sprague-Dawley rats (200–250 g)
Evidence Level
Not specified

Key Findings

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    Porcine decellularized optic nerve (DON) scaffolds exhibit uniformly distributed straight channels and microscopic pores, conducive to neural stem cell adhesion, survival, and migration.
  • 2
    DON scaffolds loaded with neurotrophin-3-overexpressing Schwann cells (SCNTs) promote directional axon regeneration and myelin regeneration in a rat model of T10 spinal cord defect.
  • 3
    Transplantation of DON scaffolds containing SCNTs reduces inflammation and the expression of chondroitin sulfate proteoglycans (CSPGs) in the injured spinal cord area.

Research Summary

This study investigates the use of a decellularized optic nerve (DON) scaffold seeded with neurotrophin-3 (NT-3)-overexpressing Schwann cells (SCs) to promote directional axon regeneration and remyelination in a rat model of spinal cord injury (SCI). In vitro, the DON scaffold exhibited a unique micro topological structure with straight, longitudinal channels and microscopic pores, which facilitated neural stem cell (NSC) adhesion, survival, and migration. It also promoted the directional growth of dorsal root ganglion (DRG) neurites and showed potential for myelin regeneration. In vivo, transplantation of the DON scaffold containing NT-3-overexpressing SCs in a rat model of T10 spinal cord defect resulted in directional growth of regenerating axons, myelin sheath recovery, and reduced inflammation and CSPGs expression.

Practical Implications

SCI Treatment

DON scaffolds loaded with SCNTs could be further explored as a novel tissue-engineering strategy for the repair of white matter SCI.

Directional Axon Regeneration

The study highlights the importance of physical channels and microstructure in scaffolds to facilitate neural cell growth and function.

Microenvironment Engineering

The research emphasizes the importance of the source of the scaffold material and the microenvironment created by the ECM in maintaining the viability of seeded cells for axonal regeneration and myelination.

Study Limitations

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