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  4. Extracellular Vesicles Can Deliver Anti-inflammatory and Anti-scarring Activities of Mesenchymal Stromal Cells After Spinal Cord Injury

Extracellular Vesicles Can Deliver Anti-inflammatory and Anti-scarring Activities of Mesenchymal Stromal Cells After Spinal Cord Injury

Frontiers in Neurology, 2019 · DOI: 10.3389/fneur.2019.01225 · Published: November 29, 2019

Spinal Cord InjuryRegenerative MedicineNeurology

Simple Explanation

Spinal cord injury leads to inflammation, which worsens damage and hinders recovery. This study explores whether extracellular vesicles (EVs) from mesenchymal stromal cells (MSCs) can replicate the anti-inflammatory and anti-scarring effects of the MSCs themselves in rats with spinal cord injury. The research found that MSC-EVs were as effective as the original MSCs in reducing inflammation for up to two weeks after the injury. The EVs also reduced pro-inflammatory cytokine expression early on. Importantly, MSC-EVs were even more effective than MSCs in reducing scarring. This suggests that EVs could be a safe and effective early treatment for traumatic spinal cord injuries.

Study Duration
2 weeks
Participants
Female F344-rats of 10–12 weeks of age
Evidence Level
Not specified

Key Findings

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    MSC-EVs effectively reduced neuroinflammation in a rat model of spinal cord injury, comparable to the effects of the parental MSCs.
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    MSC-EVs robustly decreased the expression of pro-inflammatory cytokines in the spinal cord parenchyma in the early phase of secondary damage.
  • 3
    MSC-EVs demonstrated a superior anti-scarring impact compared to parental MSCs.

Research Summary

This study investigated the potential of extracellular vesicles (EVs) derived from mesenchymal stromal cells (MSCs) to replicate the anti-inflammatory and anti-scarring effects of their parental cells in a rat model of traumatic spinal cord injury (tSCI). The results showed that MSC-EVs were as effective as MSCs in reducing inflammation and even more effective in reducing scarring. Specifically, MSC-EVs decreased the expression of pro-inflammatory cytokines in the spinal cord parenchyma. The findings suggest that MSC-EVs hold promise as a safe and druggable therapeutic option for early treatment following traumatic spinal cord injury due to their anti-inflammatory and anti-scarring properties.

Practical Implications

Therapeutic Potential

MSC-EVs show promise as a therapeutic intervention for reducing inflammation and scarring after spinal cord injury.

Drug Development

EVs offer advantages in terms of safety, manufacturing, storage, and application, making them a viable option for drug development.

Combination Therapies

MSC-EVs could be used in conjunction with other regenerative therapies to create a more favorable environment for functional recovery after spinal cord injury.

Study Limitations

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