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  4. Tissue-Engineered Regeneration of Completely Transected Spinal Cord Using Induced Neural Stem Cells and Gelatin-Electrospun Poly (Lactide-Co-Glycolide)/Polyethylene Glycol Scaffolds

Tissue-Engineered Regeneration of Completely Transected Spinal Cord Using Induced Neural Stem Cells and Gelatin-Electrospun Poly (Lactide-Co-Glycolide)/Polyethylene Glycol Scaffolds

PLoS ONE, 2015 · DOI: 10.1371/journal.pone.0117709 · Published: March 24, 2015

Spinal Cord InjuryRegenerative MedicineBiomedical

Simple Explanation

This study explores a new approach to treating spinal cord injuries using tissue engineering. The method involves using induced neural stem cells (iNSCs) and a special scaffold to help regenerate damaged spinal cord tissue. Mouse embryonic fibroblasts were reprogrammed into neural stem cells (iNSCs). These cells, along with a three-dimensional (3D) scaffold made of PLGA-PEG nanofibers, were used to promote cell growth and adhesion. The iNSC-seeded scaffolds were transplanted into rats with completely transected spinal cords. The results showed that the iNSCs survived, differentiated into neurons and glial cells, and contributed to functional recovery of the spinal cord.

Study Duration
2 months
Participants
30 adult female SD rats
Evidence Level
Not specified

Key Findings

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    Induced neural stem cells (iNSCs) can be generated from mouse embryonic fibroblasts (MEFs) through direct reprogramming.
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    PLGA-PEG nanofiber scaffolds support iNSC adhesion, growth, survival, and differentiation in vitro and in vivo.
  • 3
    Transplantation of iNSC-seeded PLGA-PEG scaffolds into transected rat spinal cords promotes functional recovery and reduces cavity formation.

Research Summary

This study aimed to investigate the potential of induced neural stem cells (iNSCs) and PLGA-PEG scaffolds for tissue-engineered regeneration of completely transected spinal cords. The results demonstrated that iNSCs can be successfully generated from MEFs, and that PLGA-PEG scaffolds provide a suitable environment for iNSC adhesion, growth, and differentiation. In vivo transplantation of iNSC-seeded scaffolds led to functional recovery, reduced cavity formation, and survival and differentiation of iNSCs into neurons and glial cells.

Practical Implications

Potential Therapeutic Application

The use of iNSCs and PLGA-PEG scaffolds represents a promising therapeutic approach for spinal cord injury.

Improved Scaffold Design

The PLGA-PEG scaffold shows superior properties compared to PLGA alone, highlighting the importance of scaffold material selection.

Cell Source Availability

iNSCs offer a readily available and ethically sound cell source for spinal cord repair compared to ESCs or iPSCs.

Study Limitations

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