Evidence map›Paper›PMID 30842428›Full record

ArticleNature communications2019

Rapid active zone remodeling consolidates presynaptic potentiation.

Mathias A Böhme, Anthony W McCarthy, Andreas T Grasskamp, Christine B Beuschel, Pragya Goel, Meida Jusyte, Desiree Laber, Sheng Huang, Ulises Rey, Astrid G Petzoldt and 8 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
8.8field-weighted citation impact, top 1% of its field
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

90 citing papers in PubMed, 148 citations in OpenAlex.

  1. Article
  2. Temporal and Cell-Specific Regulation of Synaptic Homeostasis by the Chromatin Remodeler Chd1.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Nonionic signaling rapidly remodels postsynaptic DLG to induce retrograde homeostatic plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Active Zone Maturation Controls Presynaptic Output and Release Mode and Is Regulated by Neuronal Activity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Monoamine-induced diacylglycerol signaling rapidly accumulates Unc13 in nanoclusters for fast presynaptic potentiation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
  18. Article
  19. Review
  20. Article

30 more citing papers are in PubMed but not listed here.

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

18 authors at 7 institutions in 2 countries.

Mathias A BöhmeLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125, Berlin, Germany.
Anthony W McCarthyLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125, Berlin, Germany.
Andreas T GrasskampLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125, Berlin, Germany.ORCID http://orcid.org/0000-0002-5895-6529
Christine B BeuschelNeuroCure Cluster of Excellence, Charité Universitätsmedizin, 10117, Berlin, Germany.
Pragya GoelDepartment of Neurobiology, University of Southern California, Los Angeles, CA, 90089, USA.
Meida JusyteLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125, Berlin, Germany.
Desiree LaberInstitut für Neurophysiologie, Charité Universitätsmedizin, 10117, Berlin, Germany.
Sheng HuangInstitute for Biology/Genetics, Freie Universität Berlin, 14195, Berlin, Germany.
Ulises ReyInstitute for Biology/Genetics, Freie Universität Berlin, 14195, Berlin, Germany.
Astrid G PetzoldtInstitute for Biology/Genetics, Freie Universität Berlin, 14195, Berlin, Germany.
Martin LehmannLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125, Berlin, Germany.
Fabian GöttfertDepartment of Nanobiophotonics, Max Planck Institute for Biophysical Chemistry, 37077, Göttingen, Germany.
Pejmun HaghighiBuck Institute for Research on Aging, Novato, CA, USA.
Stefan W HellDepartment of Nanobiophotonics, Max Planck Institute for Biophysical Chemistry, 37077, Göttingen, Germany.
David OwaldInstitut für Neurophysiologie, Charité Universitätsmedizin, 10117, Berlin, Germany.
Dion DickmanDepartment of Neurobiology, University of Southern California, Los Angeles, CA, 90089, USA.
Stephan J SigristNeuroCure Cluster of Excellence, Charité Universitätsmedizin, 10117, Berlin, Germany. stephan.sigrist@fu-berlin.de.
Alexander M WalterLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125, Berlin, Germany. awalter@fmp-berlin.de.
Leibniz-Forschungsinstitut für Molekulare Pharmakologie · DEFreie Universität Berlin · DECharité - Universitätsmedizin Berlin · DEMax Planck Institute for Biophysical Chemistry · DEUniversity of Southern California · USBuck Institute for Research on Aging · USMax Planck Institute of Colloids and Interfaces · DE

Funding

Molecular Mechanisms Governing the Homeostatic Control of Synaptic StrengthR01NS091546 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DICKMAN, DION KAI · 2015 to 2024
$4.3M
NINDS NIH HHS R01 NS091546
6 · The paper itself

Abstract

Neuronal communication across synapses relies on neurotransmitter release from presynaptic active zones (AZs) followed by postsynaptic transmitter detection. Synaptic plasticity homeostatically maintains functionality during perturbations and enables memory formation. Postsynaptic plasticity targets neurotransmitter receptors, but presynaptic mechanisms regulating the neurotransmitter release apparatus remain largely enigmatic. By studying Drosophila neuromuscular junctions (NMJs) we show that AZs consist of nano-modular release sites and identify a molecular sequence that adds modules within minutes of inducing homeostatic plasticity. This requires cognate transport machinery and specific AZ-scaffolding proteins. Structural remodeling is not required for immediate potentiation of neurotransmitter release, but necessary to sustain potentiation over longer timescales. Finally, mutations in Unc13 disrupting homeostatic plasticity at the NMJ also impair short-term memory when central neurons are targeted, suggesting that both plasticity mechanisms utilize Unc13. Together, while immediate synaptic potentiation capitalizes on available material, it triggers the coincident incorporation of modular release sites to consolidate synaptic potentiation.

Indexed as

AnimalsAnimals, Genetically ModifiedBehavior, AnimalDrosophila melanogasterDrosophila ProteinsFemaleLong-Term PotentiationMaleMembrane ProteinsMemory, Short-TermModels, AnimalMushroom BodiesNerve Tissue ProteinsNeuromuscular JunctionNeurotransmitter AgentsPatch-Clamp TechniquesDrosophila ProteinsMembrane ProteinsNerve Tissue ProteinsNeurotransmitter Agentsunc-13 protein, Drosophila

Identifiers

PMID30842428
PMCPMC6403334
OpenAlexW2903612916

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.