Induction of hippocampal long-term potentiation increases the morphological dynamics of microglial processes and prolongs their contacts with dendritic spines
Open accessAbstract
Recently microglia, the resident immune cells of the brain, have been recognized as multi-tasking talents that are not only essential in the diseased brain, but also actively contribute to synaptic circuit remodeling during normal brain development. It is well established that microglia dynamically scan their environment and thereby establish transient physical contacts with neuronal synapses, which may allow them to sense and influence synaptic function. However, it is unknown whether and how the morphological dynamics of microglia and their physical interactions with synapses are affected by the induction of synaptic plasticity in the adult brain. To this end, we characterized the morphological dynamics of microglia and their interactions with synapses before and after the induction of synaptic plasticity (LTP) in the hippocampus by time-lapse two-photon imaging and electrophysiological recordings in acute brain slices. We demonstrate that during hippocampal LTP microglia alter their morphological dynamics by increasing the number of their processes and by prolonging their physical contacts with dendritic spines. These effects were absent in the presence of an NMDA receptor antagonist. Taken together, this altered behavior could reflect an active microglial involvement in circuit remodeling during activity-dependent synaptic plasticity in the healthy adult brain.
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Microglia respond to increases in neural activity in the hippocampus by increasing their process numbers and prolonging their contact with synapses.
“Microglia respond to increases in neural activity in the hippocampus by increasing their process numbers and prolonging their contact with synapses (Pfeiffer et al., 2016)”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Pfeiffer et al., 2016
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References 27 · Cited by 79
- Authors
- Pfeiffer, T., Avignone, E., & Nägerl, U. V.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Nägerl, U. Valentin
- Venue
- Scientific Reports
- Published
- 2016-09-08
- Volume
- 6
- Issue
- 1
- Pages
- 32422-32422
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC5015055
- OpenAlex
- W2514203928
- Cited by
- 79
- References
- 27
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 9 · 2023: 7 · 2022: 7 · 2021: 9 · 2020: 10 · 2019: 17 · 2018: 7 · 2017: 6
- FWCI
- 5.48
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Agence Nationale de la Recherche (ANR-09-CEXC-0012, ANR-10-BLAN-1419, ANR-12-NEUR-0007, ANR-09-CEXC-012-01, ANR-12)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- microglia, hippocampal long-term potentiation, dendritic spines, synaptic plasticity, NMDA receptor, adult brain development
- MeSH terms
- Animals, Cell Communication, Electric Stimulation, Female, Hippocampus, Male, Microtomy, Synaptic Transmission, Synapses, Valine, Gene Expression, Receptors, N-Methyl-D-Aspartate, Microglia, Long-Term Potentiation, Mice, Knockout, Excitatory Postsynaptic Potentials, Tissue Culture Techniques, Dendritic Spines, Mice, Time-Lapse Imaging
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