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  4. Effects of cytokines and chemokines on migration of mesenchymal stem cells following spinal cord injury

Effects of cytokines and chemokines on migration of mesenchymal stem cells following spinal cord injury

Neural Regen Res, 2012 · DOI: 10.3969/j.issn.1673-5374.2012.14.010 · Published: May 1, 2012

Spinal Cord InjuryRegenerative MedicineGenetics

Simple Explanation

This study reviews how certain proteins called cytokines and chemokines affect the movement of mesenchymal stem cells (MSCs) to areas of damage after a spinal cord injury (SCI). MSCs are important because they can help in the healing process. The paper looks at specific cytokines and chemokines like TNF-α, VEGF, HGF, PDGF, bFGF, IGF-1, SDF-1, and MCP-1/3, and examines how they influence MSC migration towards damaged sites. Understanding these interactions could help improve treatments for SCI. The study highlights that pathways such as phosphatidylinositol 3-kinase (PI3K) and nuclear factor-κB (NF-κB) are very important in how cytokines and chemokines help MSCs move to the injured areas, suggesting these pathways could be targets for improving MSC-based therapies.

Study Duration
Not specified
Participants
Not specified
Evidence Level
Not specified

Key Findings

  • 1
    TNF-α contributes to the induction of targeted migration of MSCs towards damaged sites in the spinal cord, and activates the extracellular signal-regulated kinase and p38 pathways in MSCs.
  • 2
    VEGF-A enhances human MSC migration and the promotional effects of VEGF-A on the recovery of neurological function of the spinal cord may therefore be associated with stimulation of the migration of MSCs to the damaged region.
  • 3
    HGF regulates MSC migration by c-met and exerts chemotactic effects, contributing to the migration of MSCs to the damaged region, and regulation of the HGF/PI3K/Rac1/ signaling pathway may represent a target for enhancing MSC migration.

Research Summary

This study investigated the effects of cytokines and chemokines and their associated signaling pathways on mesenchymal stem cell migration after spinal cord injury, to determine their roles in the curative effects of mesenchymal stem cells. The results confirmed that phosphatidylinositol 3-kinase/serine/threonine protein kinases and nuclear factor-κB play crucial roles in the migration of mesenchymal stem cells induced by cytokines and chemokines. The PI3K pathway, extracellular signal-regulated kinase pathway and NF-κB in particular, appear to play important roles in cytokine and chemokine-regulated MSC migration following SCI.

Practical Implications

Enhancing MSC Migration

Understanding the roles of cytokines and chemokines can lead to strategies for improving MSC migration to damaged spinal cord areas.

Targeting Signaling Pathways

PI3K and NF-κB pathways are potential targets for therapeutic interventions to promote MSC migration.

Improving SCI Treatment

Enhancing MSC migration through cytokine and chemokine modulation may improve recovery after spinal cord injury.

Study Limitations

  • 1
    Few recent studies have reported direct evidence for the promotion of targeted MSC migration by chemokines following SCI.
  • 2
    CXCR4 expression was rare on the surface of MSCs thus limiting SDF-1/CXCR4 chemotaxis.
  • 3
    Further studies are needed to clarify if upregulated MCP-3 exerts chemotaxis by one or two receptors.

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