Cited by 160Alzheimer's disease research and treatmentsNeuroinflammation and Neurodegeneration MechanismsNeurological Disease Mechanisms and Treatments

Tau Oligomers and Fibrils Induce Activation of Microglial Cells

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Morales, Inelia, Jiménez, José M., Mancilla, Marcela, Maccioni, Ricardo B.·2013·Journal of Alzheimer’s Disease

Abstract

Neuroinflammation is a process related to the onset of several neurodegenerative disorders, including Alzheimer's disease (AD). Increasing sets of evidence support the major role of deregulation of the interaction patterns between glial cells and neurons in the pathway toward neuronal degeneration, a process we are calling neuroimmunomodulation in AD. On the basis of the hypothesis that pathological tau aggregates induce microglial activation with the subsequent events of the neuroinflammatory cascade, we have studied the effects of tau oligomeric species and filamentous structures over microglial cells in vitro. Tau oligomers and fibrils were induced by arachidonic acid and then their actions assayed upon addition to microglial cells. We showed activation of the microglia, with significant morphological alterations as analyzed by immunofluorescence. The augmentation of nitrites and the proinflammatory cytokine IL-6 was evaluated in ELISA assays. Furthermore, conditioned media of stimulated microglia cells were exposed to hippocampal neurons generating altered patterns in these cells, including shortening of neuritic processes and cytoskeleton reorganization.

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Crossref · 10.3233/jad-131843

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  • Tau oligomers and fibrils added to primary microglia directly caused microglial activation and secretion of pro-inflammatory cytokines.

    “Alternatively, tau oligomers and fibrils added into the culture of primary microglia directly caused microglial activation and secretion of pro-inflammatory cytokines.383”

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References 34 · Cited by 160

Authors
Morales, I., Jiménez, J. M., Mancilla, M., & Maccioni, R. B.
Affiliations
University of Chile (CL)
Venue
Journal of Alzheimer’s Disease
Published
2013-10-10
Volume
37
Issue
4
Pages
849-856
ISSN
  • 1387-2877 (ISSN-L)
  • 1875-8908
OpenAlex
W1542791772
Cited by
160
References
34
Citations by year
2026: 5 · 2025: 10 · 2024: 16 · 2023: 16 · 2022: 17 · 2021: 16 · 2020: 19 · 2019: 16 · 2018: 11 · 2017: 5 · 2016: 6 · 2015: 10 · 2014: 10 · 2013: 2
FWCI
6.48
Type
journal article
Language
en
Open access
Locations
  • Journal of Alzheimer s Disease (publishedVersion)
  • PubMed (publishedVersion)
  • Americanae (AECID Library) (submittedVersion, other-oa)
  • LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, other-oa)
  • Universidad de Chile (submittedVersion, cc-by-nc-nd)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
Keywords
tau oligomers, tau fibrils
MeSH terms
Amyloid, Animals, Animals, Newborn, Cells, Cultured, Humans, Organ Culture Techniques, tau Proteins, Rats, Sprague-Dawley, Microglia, Rats

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