Characterization of the microglial phenotype under specific pro-inflammatory and anti-inflammatory conditions: Effects of oligomeric and fibrillar amyloid-β
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M1 and M2 are the extremes of the differentiation spectrum of activated macrophages. Since microglia are members of the same cell lineage, we have characterized their transcription profile and their phagocytic activity under different conditions. LPS or IFN-gamma induce a M1-like phenotype, while IL-10 or IL-4 differentiate microglia towards a M2-deactivated or M2-alternatively-activated phenotype respectively. These differentiation processes also affect the Notch pathway. In order to study the polarization induced by Abeta, microglia was stimulated with different forms of the peptide. The oligomeric Abeta is a stronger M1-inductor than the fibrillar form. Moreover, a cytokine-induced anti-inflammatory environment reduces the microglial reactivity towards oligomeric Abeta.
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MHC-II expression in microglia can play an important role in innate and adaptive immune responses in PD.
“The MHC-II expression in microglia cells can play an important role in the immune responses (innate and adaptive) in PD (Michelucci et al., 2009; Harms et al., 2013; Gonzalez et al., 2015).”
From The role of microglia in retinal neurodegeneration: Alzheimer’s disease, parkinson, and glaucoma. (2017) · cites this paper as Michelucci et al., 2009
Overexpression of α-syn can induce MHC-II expression by microglia.
“In vivo and in vitro studies have demonstrated that overexpression of α-syn can induce the MHC-II expression by microglia.”
From The role of microglia in retinal neurodegeneration: Alzheimer’s disease, parkinson, and glaucoma. (2017) · cites this paper as Michelucci et al., 2009
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References 56 · Cited by 411
- Authors
- Michelucci, A., Heurtaux, T., Grandbarbe, L., Morga, E., & Heuschling, P.
- Affiliations
- University of Luxembourg (LU)
- Corresponding author
- Heuschling, Paul
- Venue
- Journal of Neuroimmunology
- Publisher
- Elsevier BV
- Published
- 2009-05
- Volume
- 210
- Issue
- 1-2
- Pages
- 3-12
- ISSN
- 0165-5728 (ISSN-L)
- OpenAlex
- W2010037905
- Cited by
- 411
- References
- 56
- Citations by year
- 2026: 9 · 2025: 21 · 2024: 30 · 2023: 23 · 2022: 34 · 2021: 21 · 2020: 26 · 2019: 24 · 2018: 17 · 2017: 20 · 2016: 21 · 2015: 29 · 2014: 34 · 2013: 30 · 2012: 35
- FWCI
- 15.17
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Neuroimmunology (publishedVersion)
- PubMed (publishedVersion)
- Open Repository and Bibliography (University of Luxembourg) (submittedVersion, other-oa)
- Funders
- Université du Luxembourg
- Fonds National de la Recherche Luxembourg
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Keywords
- microglial polarization, M1 macrophage phenotype, M2 phenotype, amyloid-beta oligomers, amyloid-beta fibrils, inflammatory cytokines, anti-inflammatory cytokines, Notch signaling, phagocytosis, gene expression profiling, Alzheimer's disease
- MeSH terms
- Alzheimer Disease, Animals, Cell Differentiation, Cell Line, Cells, Cultured, Chemotaxis, Encephalitis, Gene Expression Regulation, Gliosis, Mice, Inbred C57BL, Molecular Weight, Phenotype, Signal Transduction, Cytokines, Amyloid beta-Peptides, Microglia, Inflammation Mediators, Cell Lineage, Gene Expression Profiling, Mice, Receptors, Notch
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