Evidence map›Paper›PMID 40185633›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Intracellular Spermine Is a Key Player in GSG1L's Regulation of Calcium-Permeable AMPAR Channel Conductance and Recovery from Desensitization.

Thomas P McGee, Cecile Bats, Mark Farrant, Stuart G Cull-Candy

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Thomas P McGeeDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, United Kingdom.ORCID https://orcid.org/0000-0002-4051-6728
Cecile BatsDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, United Kingdom.ORCID https://orcid.org/0000-0002-2246-7248
Mark FarrantDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, United Kingdom s.cull-candy@ucl.ac.uk m.farrant@ucl.ac.uk.ORCID https://orcid.org/0000-0002-9918-0376
Stuart G Cull-CandyDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, United Kingdom s.cull-candy@ucl.ac.uk m.farrant@ucl.ac.uk.ORCID https://orcid.org/0000-0002-0831-8326

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcium-permeable AMPA-type glutamate receptors (CP-AMPARs) contribute to excitatory synaptic transmission and play pivotal roles in normal and detrimental forms of plasticity. Most AMPARs are associated with auxiliary subunits. Transmembrane AMPAR regulatory proteins (TARPs), the prototypical auxiliary subunits, enhance current through CP-AMPAR channels by increasing single-channel conductance and relieving the characteristic voltage-dependent block by endogenous intracellular polyamines, such as spermine. In contrast, the atypical auxiliary subunit GSG1L negatively regulates CP-AMPARs, suppressing current flow by promoting polyamine block and reducing channel conductance. Here, we investigated the role of polyamines in these opposing effects. We show that, in the absence of auxiliary subunits, intracellular spermine decreases CP-AMPAR single-channel conductance. This effect is prevented by the presence of TARPs but enhanced by the presence of GSG1L. Unexpectedly, intracellular spermine is necessary for both GSG1L's attenuation of CP-AMPAR channel conductance and its characteristic slowing of recovery from desensitization. These various effects are determined by specific residues within the channel's selectivity filter and within GSG1L's C-tail. Together, our findings reveal that intracellular polyamines play an essential role in GSG1L's unique ability to negatively regulate many of the key properties of CP-AMPARs.

Indexed as

CalciumIntracellular FluidReceptors, AMPASpermineAnimalsHEK293 CellsHumansMembrane PotentialsPatch-Clamp TechniquesCalciumReceptors, AMPASpermineAMPA receptor auxiliary subunitsdesensitizationGSG1Lpolyaminessingle-channelTARPs

Identifiers

PMID40185633
PMCPMC12060639

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.