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Isolation of Cortical Microglia with Preserved Immunophenotype and Functionality From Murine Neonates
Published on: January 30, 2014
The Influence of Virus Infection on Microglia and Accelerated Brain Aging
Luis Filgueira1, Alexey Larionov1, Nils Lannes1
1Anatomy, Faculty of Science and Medicine, University of Fribourg, 1700 Fribourg, Switzerland.
Abstract:
Microglia are the resident immune cells of the central nervous system contributing substantially to health and disease. There is increasing evidence that inflammatory microglia may induce or accelerate brain aging, by interfering with physiological repair and remodeling processes. Many viral infections affect the brain and interfere with microglia functions, including human immune deficiency virus, flaviviruses, SARS-CoV-2, influenza, and human herpes viruses. Especially chronic viral infections causing low-grade neuroinflammation may contribute to brain aging. This review elucidates the potential role of various neurotropic viruses in microglia-driven neurocognitive deficiencies and possibly accelerated brain aging.
Insights
Inflammatory microglia, driven by viral infections, may accelerate brain aging and cause neurocognitive deficits. This review explores the link between neurotropic viruses and microglia-mediated brain aging.
Area of Science:
- Neuroscience
- Immunology
- Virology
Background:
- Microglia are key immune cells in the central nervous system (CNS).
- Neuroinflammation driven by microglia is implicated in brain aging.
- Viral infections frequently impact CNS and microglia function.
Purpose of the Study:
- To review the role of neurotropic viruses in microglia-driven neurocognitive deficiencies.
- To elucidate the potential contribution of viral infections to accelerated brain aging.
Main Methods:
- Literature review of studies on microglia, neuroinflammation, viral infections, and brain aging.
- Synthesis of evidence linking specific neurotropic viruses to microglia dysfunction.
- Analysis of mechanisms by which viruses may induce neuroinflammation and cognitive decline.
Main Results:
- Various neurotropic viruses (e.g., HIV, flaviviruses, SARS-CoV-2, influenza, herpesviruses) interfere with microglia functions.
- Chronic viral infections can cause persistent low-grade neuroinflammation.
- This neuroinflammation may disrupt physiological brain repair processes, contributing to aging.
Conclusions:
- Neurotropic viruses can dysregulate microglia, potentially leading to neurocognitive deficiencies.
- Viral-induced microglia activation is a significant factor in accelerated brain aging.
- Further research is needed to fully understand and target these mechanisms.
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