Spinal Cord Research Help
AboutCategoriesLatest ResearchContact
Subscribe
Spinal Cord Research Help

Making Spinal Cord Injury (SCI) Research Accessible to Everyone. Simplified summaries of the latest research, designed for patients, caregivers and anybody who's interested.

Quick Links

  • Home
  • About
  • Categories
  • Latest Research
  • Disclaimer

Contact

  • Contact Us
© 2025 Spinal Cord Research Help

All rights reserved.

  1. Home
  2. Research
  3. Aging
  4. Immunosenescence of microglia and macrophages: impact on the ageing central nervous system

Immunosenescence of microglia and macrophages: impact on the ageing central nervous system

Brain, 2016 · DOI: 10.1093/brain/awv395 · Published: January 29, 2016

AgingImmunologyNeurology

Simple Explanation

As we age, the central nervous system (CNS) experiences a decline in both gray and white matter, leading to cognitive impairment. This decline is often worsened by neurological disorders such as Alzheimer's disease and multiple sclerosis. Macrophages and microglia, which are immune cells in the CNS, play a role in these conditions. This article explores how macrophages and microglia age differently and how these differences impact the aging CNS. It suggests that targeting these differences with specific therapies might help rejuvenate these cells and improve neurological repair. The authors propose therapeutic strategies that selectively target these diverse mechanisms may rejuvenate macrophages and microglia for repair in the ageing central nervous system.

Study Duration
Not specified
Participants
Not specified
Evidence Level
Not specified

Key Findings

  • 1
    Macrophages and microglia, two types of immune cells in the brain, age in distinct ways, with macrophages showing diminished pro-inflammatory responses and microglia exhibiting an exaggerated pro-inflammatory response with age.
  • 2
    Ageing microglia and macrophages exhibit deficits in phagocytic and chemotactic functions.
  • 3
    The mechanisms behind these age-related changes vary, ranging from changes in the environment surrounding the cells to intrinsic changes within the cells themselves, such as genomic instability.

Research Summary

Aging in the central nervous system (CNS) leads to a loss of gray and white matter, contributing to cognitive decline, which is further exacerbated by neurological disorders. This is accompanied by an inflammatory response involving macrophages and microglia. The review highlights that macrophages and microglia age differently, with macrophages showing diminished responses and microglia increasing pro-inflammatory cytokine expression while reducing chemotactic and phagocytic activities. The authors propose therapeutic strategies to rejuvenate macrophages and microglia, potentially preserving neurological integrity and promoting regeneration in the aging CNS.

Practical Implications

Targeted Therapies

Developing therapies that specifically target the distinct aging mechanisms of macrophages and microglia could lead to more effective treatments for age-related neurological disorders.

Rejuvenation Strategies

Rejuvenating aging macrophage/microglia may preserve neurological integrity and promote regeneration in the ageing central nervous system.

Enhancing Phagocytosis

Stimulating microglia to phagocytose inhibitory myelin debris without an excessive pro-inflammatory cytokine response could enhance axon regeneration and remyelination.

Study Limitations

  • 1
    Methodological limitations of previous studies have not permitted their separate identification [macrophages and microglia]
  • 2
    Though difficult to distinguish between peripherally-derived macrophages and CNS-resident microglia, in vivo studies show that the capacity for ageing macrophages and microglia to adopt a regulatory phenotype is compromised with ageing.
  • 3
    Reasons for these differences are unknown, but may be a function of the microenvironment.

Your Feedback

Was this summary helpful?

Back to Aging