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Mechanisms of postsynaptic localization of AMPA-type glutamate receptors and their regulation during long-term potentiation

Buonarati, Olivia R., Hammes, Erik A., Watson, Jake F., Greger, Ingo H., Hell, Johannes W.·2019·Science Signaling
DOI 10.1126/scisignal.aar6889PMC PMC7175813
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Abstract

Postsynaptic anchoring of AMPA receptors determines synaptic strength as related to learning.

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Crossref · 10.1126/scisignal.aar6889

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  • AMPA receptors are rapidly inserted into the postsynaptic membrane in response to synaptic activity, a process critical for long-term potentiation.

    “AMPA receptors are rapidly inserted into the postsynaptic membrane in response to synaptic activity, a process critical for long-term potentiation”

    From PI(3)P coordinates SNX17- and SNX27-dependent protein recycling for long-term synaptic plasticity (2025) · cites this paper as Buonarati et al., 2019

    The Introduction’s “Secretory trafficking of AMPARs” section says stimulated exocytosis and subsequent surface diffusion increase synaptic AMPAR content during LTP. But “Regulation of postsynaptic AMPAR content” distinguishes the phases: the first 2–3 minutes depend on lateral diffusion, not acute exocytosis, which contributes later. Thus the claim captures activity-dependent receptor recruitment but overstates rapid insertion directly into the postsynaptic membrane. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

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Metadata

Authors
Buonarati, O. R., Hammes, E. A., Watson, J. F., Greger, I. H., & Hell, J. W.
Affiliations
  • Department of Pharmacology, University of California at Davis, Davis, CA 95616-8636, USA.
  • Neurobiology Division, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
ORCID
Venue
Science Signaling
Publisher
American Association for the Advancement of Science (AAAS)
Published
2019-01
Volume
12
Issue
562
ISSN
  • 1945-0877
  • 1937-9145
DOI
10.1126/scisignal.aar6889
PMC
PMC7175813
Cited by
86
References
20
Language
en
Funders
  • NIH Office of the Director (NIH R01 MH097887, NIH R01 NS078792, NIH R01 AG055357)
  • BBSRC (BBSRC BB/N002113/1)
  • MRC (MRC MC_U105174197)

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