Fractalkine‐induced activation of the phosphatidylinositol‐3 kinase pathway attentuates microglial activation in vivo and in vitro
Abstract
Several neurodegenerative disorders are associated with evidence of inflammation, one feature of which is increased activation of microglia, the most likely cellular source of inflammatory cytokines like interleukin‐1β. It is now recognized that interaction of microglia with other cells contributes to maintenance of microglia in a quiescent state and the complementary distribution of the chemokine, fractalkine (CX 3 CL1) on neurons and its receptor (CX 3 CR1) on microglia, suggests that this interaction may play a role in modulating microglial activation. Here we demonstrate that both soluble and membrane‐bound fractalkine attenuate lipopolysaccharide‐induced microglial activation in vitro. We also show that fractalkine expression is reduced in the brain of aged rats and this is accompanied by an age‐related increase in microglial activation. Treatment of aged rats with fractalkine attenuates the age‐related increase in microglial activation and the evidence indicates that fractalkine‐induced activation of the phosphatidylinositol‐3 kinase pathway is required to maintain microglia in a quiescent state both in vivo and in vitro.
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Immunosuppressor proteins including CX3CL1 and CD47 (to control microglial and macrophage function) and CFH (to control T-cell activation and block complement triggers) are already activated by neurodegeneration and block overproduction of pro-inflammatory signals.
“The immunosuppressor proteins, including CX3CL1 and CD47 (to control microglial and macrophage function) and CFH (to control T-cell activation and block complement triggers), are already activated by neurodegeneration and block the overproduction of pro-inflammatory signals (such as inducible nitric oxide synthase, interleukin (IL)-1β, tumor necrosis factor-α (TNF-α), and IL-6) [61,62].”
From Risk mitigation of immunogenicity: a key to personalized retinal gene therapy (2021) · cites this paper as [61]
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- Authors
- Lyons, A., Lynch, A. M., Downer, E. J., Hanley, R., O’Sullivan, J. B., Smith, A., & Lynch, M. A.
- Affiliations
- Trinity College Dublin (IE)
- Corresponding author
- Lynch, Marina A.
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 2009-08-10
- Volume
- 110
- Issue
- 5
- Pages
- 1547-1556
- ISSN
- 0022-3042 (ISSN-L)
- 1471-4159
- OpenAlex
- W2036586619
- Cited by
- 202
- References
- 46
- Citations by year
- 2026: 8 · 2025: 8 · 2024: 16 · 2023: 9 · 2022: 15 · 2021: 12 · 2020: 12 · 2019: 16 · 2018: 11 · 2017: 13 · 2016: 12 · 2015: 5 · 2014: 10 · 2013: 16 · 2012: 11
- FWCI
- 8.31
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Science Foundation Ireland
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- fractalkine, CX3CR1, microglial activation, phosphatidylinositol 3-kinase pathway, neuroinflammation, lipopolysaccharide, aging, neurodegenerative diseases, IL-1β, microglia-neuron interaction
- MeSH terms
- Age Factors, Aging, Animals, Animals, Newborn, Cells, Cultured, Enzyme Activation, Lipopolysaccharides, Male, Membrane Proteins, Solubility, Signal Transduction, Rats, Wistar, Microglia, Phosphatidylinositol 3-Kinases, Rats, Chemokine CX3CL1
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