Evidence map›Paper›PMID 41074974›Full record

ArticleCellular and molecular life sciences : CMLS2025

Temporal and protein-specific S-palmitoylation supports synaptic and neural network plasticity.

Agata Pytyś, Rabia Ijaz, Anna Buszka, Jacek Miłek, Izabela Figiel, Patrycja Wardaszka-Pianka, Matylda Roszkowska, Natalia Mierzwa, Adam Wojtas, Eli Kerstein and 6 more

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Post-Translational Modifications in Traumatic Brain Injury: Decoding the Proteomic Landscape and Molecular Mechanisms of Secondary Injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  2. Review
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

16 authors.

Agata PytyśLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Rabia IjazLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Anna BuszkaLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Jacek MiłekDepartment of Animal Physiology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
Izabela FigielLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Patrycja Wardaszka-PiankaDepartment of Animal Physiology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
Matylda RoszkowskaLaboratory of Neurobiology, BRAINCITY, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Natalia MierzwaLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Adam WojtasLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Eli KersteinDepartment of Physics, Georgetown University, Washington, D.C, USA.
Remigiusz SerwaProteomics Core Facility, The International Institute of Molecular Mechanisms and Machines of the Polish Academy of Sciences, Warsaw, Poland.
Katarzyna KalitaLaboratory of Neurobiology, BRAINCITY, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Rhonda DzakpasuDepartment of Physics, Georgetown University, Washington, D.C, USA.
Magdalena DziembowskaDepartment of Animal Physiology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
Jakub WłodarczykLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Tomasz WójtowiczLaboratory of Cell Biophysics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland. t.wojtowicz@nencki.edu.pl.ORCID http://orcid.org/0000-0003-1128-4363

Funding

Narodowe Centrum Nauki 2019/34/E/NZ4/00387
6 · The paper itself

Abstract

backgroundSynaptic plasticity, a fundamental process underlying learning and memory, depends on activity-driven changes in neural connectivity. S-palmitoylation, a reversible post-translational lipid modification, modulates synaptic protein function by influencing protein conformation, localization, trafficking, and molecular interactions. Despite its known significance in neuronal function, the temporal and protein-specific dynamics of S-palmitoylation during synaptic plasticity remain poorly understood. METHODOLOGY & PRINCIPAL

findingsUsing electrophysiological methods, molecular biology, proteomics, and imaging across various models (neuronal cultures, hippocampal slices, and synaptoneurosomes), we investigated S-palmitoylation during synaptic activity. Induction of long-term potentiation (LTP) resulted in protein-specific palmitoylation changes without altering global levels. In hippocampal slices, synaptophysin and PSD95 displayed distinct temporal patterns of palmitoylation, influenced by LTP. Deacylation experiments using N-(tert-butyl)hydroxylamine (NtBuHA) demonstrated that protein S-palmitoylation is crucial for organizing neuronal spiking and enabling LTP, particularly in the stratum radiatum. Mass spectrometry of synaptoneurosomes revealed a palmitoylome including over 700 proteins, with stimulation-induced predominant depalmitoylation. Differentially palmitoylated proteins were associated with synaptic vesicle cycling, cytoskeletal dynamics, and neurotransmitter release. What is interesting is that synaptoneurosomes contained active palmitoylation machinery, supporting rapid, target-specific responses to NMDA receptor activation.

conclusionsTemporal and protein-specific S-palmitoylation emerges as a vital mechanism for synaptic plasticity, contributing to neuronal network function and memory formation. These findings elucidate how palmitoylation acts as a dynamic regulator of synaptic activity and offer insights into its regulation. The study highlights the potential of targeting palmitoylation pathways for enhancing neuronal function.

Indexed as

LipoylationNerve NetNeuronal PlasticitySynapsesAnimalsCells, CulturedDisks Large Homolog 4 ProteinHippocampusLong-Term PotentiationMaleMembrane ProteinsMiceNeuronsProtein Processing, Post-TranslationalRatsSynaptophysinDisks Large Homolog 4 ProteinDlg4 protein, ratMembrane ProteinsSynaptophysinAcyl-biotin exchange assayMass spectrometryNMDAR-dependent LTP (long-term potentiation)Post-translational modifications (PTMs)Protein acylationSynaptoneurosomes

Identifiers

PMID41074974
PMCPMC12515174

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.