An emerging role for microglia in stress-effects on memory

Jeniffer Sanguino-Gomez*, Jacobus C. Buurstede, Oihane Abiega, Carlos P. Fitzsimons, Paul J. Lucassen, Bart J. L. Eggen, Sylvie L. Lesuis, Onno C. Meijer, Harm J. Krugers

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

12 Citations (Scopus)
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Abstract

Stressful experiences evoke, among others, a rapid increase in brain (nor)epinephrine (NE) levels and a slower increase in glucocorticoid hormones (GCs) in the brain. Microglia are key regulators of neuronal function and contain receptors for NE and GCs. These brain cells may therefore potentially be involved in modulating stress effects on neuronal function and learning and memory. In this review, we discuss that stress induces (1) an increase in microglial numbers as well as (2) a shift toward a pro-inflammatory profile. These microglia have (3) impaired crosstalk with neurons and (4) disrupted glutamate signaling. Moreover, microglial immune responses after stress (5) alter the kynurenine pathway through metabolites that impair glutamatergic transmission. All these effects could be involved in the impairments in memory and in synaptic plasticity caused by (prolonged) stress, implicating microglia as a potential novel target in stress-related memory impairments.

Original languageEnglish
Pages (from-to)2491-2518
Number of pages28
JournalEuropean Journal of Neuroscience
Volume55
Issue number9-10
Early online date16-Mar-2021
DOIs
Publication statusPublished - May-2022

Keywords

  • corticosterone
  • glucocorticoids
  • learning
  • norepinephrine
  • synapses
  • LONG-TERM POTENTIATION
  • NECROSIS-FACTOR-ALPHA
  • ADULT HIPPOCAMPAL NEUROGENESIS
  • AMPA RECEPTOR FUNCTION
  • SYNAPTIC PLASTICITY
  • INFLAMMATORY RESPONSE
  • ALZHEIMERS-DISEASE
  • RAT HIPPOCAMPUS
  • TNF-ALPHA
  • GLUCOCORTICOID-RECEPTORS

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