Evidence map›Paper›PMID 37210439›Full record

ArticleNature communications2023

Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis.

Tyler H Ogunmowo, Haoyuan Jing, Sumana Raychaudhuri, Grant F Kusick, Yuuta Imoto, Shuo Li, Kie Itoh, Ye Ma, Haani Jafri, Matthew B Dalva and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
10.4field-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

33 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Deciphering the Nanoscale Architecture of Presynaptic Actin Using a Micropatterned Presynapse-on-Glass Model.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  8. Article
  9. Article
  10. Molecular Physiology of the Neuronal Synapse.Current issues in molecular biology · 2026
    Review
  11. Review
  12. Article
  13. Article
  14. CRISPR-edited iPSCs reveal BSN gene mutations induce neuronal hyperexcitability via astrocyte lipid accumulation.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  15. Biogenesis and reformation of synaptic vesicles.The Journal of physiology · 2025
    Review
  16. Article
  17. Ultrastructural membrane dynamics of mouse and human cortical synapses.bioRxiv : the preprint server for biology · 2025
    Article
  18. Article
  19. Review
  20. 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

14 authors at 4 institutions in 1 country.

Tyler H Ogunmowo *Department of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Haoyuan Jing *Department of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Sumana Raychaudhuri *Department of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Grant F Kusick *Department of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.ORCID 0000-0002-4312-3495
Yuuta ImotoDepartment of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Shuo LiDepartment of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Kie ItohDepartment of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Ye MaDepartment of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD, US.
Haani JafriDepartment of Neuroscience and Jefferson Synaptic Biology Center, Thomas Jefferson University, Philadelphia, PA, US.
Matthew B DalvaDepartment of Neuroscience and Jefferson Synaptic Biology Center, Thomas Jefferson University, Philadelphia, PA, US.ORCID 0000-0002-7737-8787
Edwin R ChapmanDepartment of Neuroscience, University of Wisconsin-Madison, Madison, WI, US.ORCID 0000-0001-9787-8140
Taekjip HaDepartment of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD, US.ORCID 0000-0003-2195-6258
Shigeki WatanabeDepartment of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US. shigeki.watanabe@jhmi.edu.ORCID 0000-0001-7580-8141
Jian LiuDepartment of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD, US. jliu187@jhmi.edu.ORCID 0000-0003-2935-0349
Johns Hopkins University · USHoward Hughes Medical Institute · USThomas Jefferson University · USTulane University · US

Funding

BIOCHEMISTRY, CELLULAR AND MOLECULAR BIOLOGY PROGRAMT32GM007445 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GREEN, RACHEL · 1985 to 2021
$24.1M
Synaptotagmin C2B Domain as a Ca2+ Sensing ModuleR01MH061876 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI Edwin R Chapman · 2002 to 2026
$7.7M
Cell-Contact Mediated Mechanisms Assembling Synapses (R01DA022727)R01DA022727 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI DALVA, MATTHEW B · 2007 to 2025
$5.2M
Structure and dynamics of exocytotic fusion poresR35NS097362 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI CHAPMAN, EDWIN R · 2017 to 2024
$4.6M
Reviving electron microscopy for synaptic cell biologyDP2NS111133 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WATANABE, SHIGEKI · 2018 to 2018
$2.5M
Examining the Function of Biological Sex Specific Genes: the NLGN4sR01NS106906 · NINDS · TULANE UNIVERSITY OF LOUISIANA · PI DALVA, MATTHEW B · 2018 to 2022
$2.1M
Spatial and molecular determinants of fusion probability and timingR01NS105810 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WATANABE, SHIGEKI · 2018 to 2022
$1.8M
Predictive multi-scale model of focal adhesion-based durotaxisR01GM148459 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Jian Liu · 2023 to 2026
$1.6M
Howard Hughes Medical InstituteNIDA NIH HHS R01 DA022727NIGMS NIH HHS R01 GM148459NIGMS NIH HHS T32 GM007445NIMH NIH HHS R01 MH061876NINDS NIH HHS DP2 NS111133NINDS NIH HHS R01 NS105810NINDS NIH HHS R01 NS106906NINDS NIH HHS R35 NS097362
6 · The paper itself

Abstract

Compensatory endocytosis keeps the membrane surface area of secretory cells constant following exocytosis. At chemical synapses, clathrin-independent ultrafast endocytosis maintains such homeostasis. This endocytic pathway is temporally and spatially coupled to exocytosis; it initiates within 50 ms at the region immediately next to the active zone where vesicles fuse. However, the coupling mechanism is unknown. Here, we demonstrate that filamentous actin is organized as a ring, surrounding the active zone at mouse hippocampal synapses. Assuming the membrane area conservation is due to this actin ring, our theoretical model suggests that flattening of fused vesicles exerts lateral compression in the plasma membrane, resulting in rapid formation of endocytic pits at the border between the active zone and the surrounding actin-enriched region. Consistent with model predictions, our data show that ultrafast endocytosis requires sufficient compression by exocytosis of multiple vesicles and does not initiate when actin organization is disrupted, either pharmacologically or by ablation of the actin-binding protein Epsin1. Our work suggests that membrane mechanics underlie the rapid coupling of exocytosis to endocytosis at synapses.

Indexed as

ActinsSynaptic VesiclesAnimalsCell MembraneEndocytosisExocytosisMiceSynapsesActins

Identifiers

PMID37210439
PMCPMC10199930
OpenAlexW4377138052

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.