Cited by 411Neuroinflammation and Neurodegeneration MechanismsAlzheimer's disease research and treatmentsInflammasome and immune disorders

Characterization of the microglial phenotype under specific pro-inflammatory and anti-inflammatory conditions: Effects of oligomeric and fibrillar amyloid-β

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Michelucci, Alessandro, Heurtaux, Tony, Grandbarbe, Luc, Morga, Eleonora, Heuschling, Paul·2009·Journal of Neuroimmunology

Abstract

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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Crossref · 10.1016/j.jneuroim.2009.02.003

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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
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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