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  4. Hierarchically aligned fibrin nanofiber hydrogel accelerated axonal regrowth and locomotor function recovery in rat spinal cord injury

Hierarchically aligned fibrin nanofiber hydrogel accelerated axonal regrowth and locomotor function recovery in rat spinal cord injury

International Journal of Nanomedicine, 2018 · DOI: 10.2147/IJN.S159356 · Published: May 7, 2018

Spinal Cord InjuryBiomedical

Simple Explanation

This study focuses on developing biomaterials to mimic the functions of the extracellular matrix, aiming to deliver regulatory signals for tissue regeneration, particularly in the context of spinal cord injury. A three-dimensional hierarchically aligned fibrin hydrogel (AFG) was created to mimic the natural environment of spinal cord tissue, featuring oriented topography and soft stiffness to promote cell invasion and axonal regrowth. The AFG scaffold facilitated directional host cell invasion, vascular system reconstruction, and axonal regrowth, leading to improved locomotor function recovery in rats with spinal cord injuries.

Study Duration
8 weeks
Participants
Adult female SD rats (200–230 g)
Evidence Level
Not specified

Key Findings

  • 1
    Host cells rapidly invaded the aligned fibrin hydrogels, forming aligned tissue cables within the first week, followed by axonal regrowth in the rat spinal cord injury model.
  • 2
    New axon regrowth was observed in the oriented tissue cables, penetrating throughout the lesion site by 8 weeks, indicated by abundant NF- and GAP-43-positive staining.
  • 3
    Locomotor performance in the AFG group recovered much faster compared to the control and random fibrin hydrogel (RFG) groups, starting from 2 weeks after surgery.

Research Summary

The study fabricated a three-dimensional hierarchically aligned fibrin hydrogel (AFG) to mimic the spinal cord tissue environment and promote tissue regeneration after spinal cord injury. Implantation of the AFG in a rat spinal cord injury model resulted in rapid host cell invasion, aligned tissue cable formation, vascular system reconstruction, and accelerated axonal regrowth. The AFG scaffold improved locomotor function recovery in rats, demonstrating its potential for promoting axon regeneration and functional restoration after spinal cord injury.

Practical Implications

Therapeutic strategy

AFG implantation could serve as a promising therapeutic strategy for spinal cord injury by providing a regenerative microenvironment.

Biomaterial design

The study highlights the importance of biomaterial mechanical properties and topography in directing cell behavior and tissue regeneration.

Clinical translation

The AFG scaffold design could be further developed and translated into clinical applications for promoting spinal cord regeneration in humans.

Study Limitations

  • 1
    Limited to rat model, may not fully translate to human physiology.
  • 2
    The long-term effects of AFG implantation beyond 8 weeks were not assessed.
  • 3
    The study did not investigate the specific mechanisms of AFG-induced axonal regeneration.

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