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  4. Advances in the research of the role of macrophage/microglia polarization-mediated inflammatory response in spinal cord injury

Advances in the research of the role of macrophage/microglia polarization-mediated inflammatory response in spinal cord injury

Frontiers in Immunology, 2022 · DOI: 10.3389/fimmu.2022.1014013 · Published: December 1, 2022

Spinal Cord InjuryImmunologyNeurology

Simple Explanation

Following a spinal cord injury (SCI), the body's inflammatory response plays a significant role in determining the extent of damage and potential for recovery. Macrophages and microglia, types of immune cells, are key players in this response. These cells can adopt different states, known as M1 and M2, each with distinct effects. M1 macrophages/microglia promote inflammation and tissue damage, while M2 macrophages/microglia reduce inflammation and support tissue repair. The shift from M1 to M2 is believed to be beneficial for recovery after SCI. Understanding how to influence this shift could lead to new treatments. This review discusses the roles of macrophages/microglia in SCI and explores potential molecular mechanisms that control their polarization. It also highlights neuroprotective therapies that modulate macrophage/microglia polarization, aiming to provide insights for developing new SCI treatments.

Study Duration
Not specified
Participants
Not specified
Evidence Level
Systematic Review

Key Findings

  • 1
    M1 macrophages/microglia exacerbate inflammation and tissue damage after SCI by releasing pro-inflammatory cytokines, while M2 macrophages/microglia promote tissue repair and reduce inflammation by releasing anti-inflammatory cytokines.
  • 2
    The transition from M1 to M2 macrophages/microglia is associated with reduced secondary damage and improved locomotor recovery after SCI.
  • 3
    Several neuroprotective therapies, including delivery of molecules to alter macrophage/microglia phenotype, mesenchymal stem cell and exosome therapy, and microRNA modulation, can influence macrophage/microglia polarization and promote SCI repair.

Research Summary

Spinal cord injury (SCI) leads to neurological dysfunction, and neuroinflammation plays a crucial role in the extent of damage. Macrophages/microglia, key immune cells, polarize into pro-inflammatory M1 and anti-inflammatory M2 phenotypes, influencing SCI outcomes. M1 macrophages/microglia exacerbate SCI through pro-inflammatory cytokine release, while M2 macrophages/microglia promote tissue repair and reduce inflammation. Shifting the balance from M1 to M2 is a potential therapeutic strategy. Neuroprotective therapies targeting macrophage/microglia polarization, such as molecule delivery, MSCs, exosomes, and miRNAs, show promise in promoting neural tissue regeneration and functional recovery after SCI, but careful regulation of phenotype balance is essential.

Practical Implications

Therapeutic Target Identification

Identifying specific molecular mechanisms that regulate macrophage/microglia polarization can help in developing targeted therapies for SCI.

Development of Neuroprotective Strategies

Modulating macrophage/microglia polarization using molecule delivery, MSCs, exosomes, or miRNAs can improve neural tissue regeneration and functional recovery after SCI.

Personalized Treatment Approaches

Understanding the specific phenotypes of macrophages/microglia present in individual SCI patients can help in tailoring treatment strategies to promote optimal recovery.

Study Limitations

  • 1
    The M1/M2 paradigm may be oversimplified, as macrophages/microglia can exist in a continuum of activation states.
  • 2
    Rodent models may not fully reflect the complexity of macrophage/microglia responses in humans.
  • 3
    Excessive or prolonged M2 polarization may contribute to scar formation and hinder axonal regeneration.

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