High-resolution imaging and manipulation of endogenous AMPA receptor surface mobility during synaptic plasticity and learning
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Abstract
Regulation of synaptic neurotransmitter receptor content is a fundamental mechanism for tuning synaptic efficacy during experience-dependent plasticity and behavioral adaptation. However, experimental approaches to track and modify receptor movements in integrated experimental systems are limited. Exploiting AMPA-type glutamate receptors (AMPARs) as a model, we generated a knock-in mouse expressing the biotin acceptor peptide (AP) tag on the GluA2 extracellular N-terminal. Cell-specific introduction of biotin ligase allows the use of monovalent or tetravalent avidin variants to respectively monitor or manipulate the surface mobility of endogenous AMPAR containing biotinylated AP–GluA2 in neuronal subsets. AMPAR immobilization precluded the expression of long-term potentiation and formation of contextual fear memory, allowing target-specific control of the expression of synaptic plasticity and animal behavior. The AP tag knock-in model offers unprecedented access to resolve and control the spatiotemporal dynamics of endogenous receptors, and opens new avenues to study the molecular mechanisms of synaptic plasticity and learning.
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Interfering with the surface diffusion of AMPARs by receptor cross-linking markedly impairs LTP.
“Consistent with this result is the finding that interfering with the surface diffusion of AMPARs by receptor cross-linking markedly impairs LTP (345–347).”
From Synaptic memory and CaMKII (2023) · cites this paper as [346]
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Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126 · see citing works
- Authors
- Getz, A. M., Ducros, M., Breillat, C., Lampin-Saint-Amaux, A., Daburon, S., François, U., Nowacka, A., Fernández-Monreal, M., Hosy, E., Lanore, F., Zieger, H. L., Sainlos, M., Humeau, Y., & Choquet, D.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Université de Bordeaux, CNRS, INSERM, Bordeaux Imaging Center (BIC), UAR 3420, US 4, F-33000 Bordeaux, France.
- Corresponding author
- Choquet, Daniel
- ORCID
- Venue
- Science Advances
- Published
- 2022-07-29
- Volume
- 8
- Issue
- 30
- Pages
- eabm5298-eabm5298
- ISSN
- 2375-2548 (ISSN-L)
- PMC
- PMC9328687
- OpenAlex
- W4288050293
- Cited by
- 55
- References
- 11
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- FWCI
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- journal article
- Language
- en
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- doi.org
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- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
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- Funders
- Agence Nationale de la Recherche (ANR-16, ANR-10-LABX-0043, ANR-10-INBS-0004, ANR-16-CE16-0026)
- Université de Bordeaux
- Canadian Institutes of Health Research
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Biotin and Related Studies
- Keywords
- AMPA receptors, GluA2, biotin acceptor peptide, synaptic plasticity, long-term potentiation, contextual fear memory, avidin, receptor immobilization, knock-in mice, glutamate receptors, learning
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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