Evidence map›Paper›PMID 25296249›Full record

ArticleNature2014

Clathrin regenerates synaptic vesicles from endosomes.

Shigeki Watanabe, Thorsten Trimbuch, Marcial Camacho-Pérez, Benjamin R Rost, Bettina Brokowski, Berit Söhl-Kielczynski, Annegret Felies, M Wayne Davis, Christian Rosenmund, Erik M Jorgensen

Abstract read
In one paragraph

Article in Nature, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed
14.0field-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

183 citing papers in PubMed, 348 citations in OpenAlex.

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  18. Biogenesis and reformation of synaptic vesicles.The Journal of physiology · 2025
    Review
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123 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Shigeki WatanabeDepartment of Biology and Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112-0840, USA.
Thorsten TrimbuchNeuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Marcial Camacho-PérezNeuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Benjamin R Rost1] Neuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany [2] German Center for Neurodegenerative Diseases (DZNE), 10117 Berlin, Germany.
Bettina BrokowskiNeuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Berit Söhl-KielczynskiNeuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Annegret FeliesNeuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
M Wayne DavisDepartment of Biology and Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112-0840, USA.
Christian RosenmundNeuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Erik M JorgensenDepartment of Biology and Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112-0840, USA.
Charité - Universitätsmedizin Berlin · DEHoward Hughes Medical Institute · USUniversity of Utah · US

Funding

SYNAPTIC FUNCTION IN THE NEMATODE C. ELEGANSR01NS034307 · NINDS · UNIVERSITY OF UTAH · PI JORGENSEN, ERIK M · 1995 to 2024
$5.8M
SYNAPTIC FUNCTION IN THE NEMATODE C. ELEGANSR37NS034307 · NINDS · UNIVERSITY OF UTAH · PI JORGENSEN, ERIK M · 1999 to 2009
$3.3M
European Research Council 249939Howard Hughes Medical InstituteNINDS NIH HHS NS034307NINDS NIH HHS R01 NS034307NINDS NIH HHS R37 NS034307
6 · The paper itself

Abstract

Ultrafast endocytosis can retrieve a single, large endocytic vesicle as fast as 50-100 ms after synaptic vesicle fusion. However, the fate of the large endocytic vesicles is not known. Here we demonstrate that these vesicles transition to a synaptic endosome about one second after stimulation. The endosome is resolved into coated vesicles after 3 s, which in turn become small-diameter synaptic vesicles 5-6 s after stimulation. We disrupted clathrin function using RNA interference (RNAi) and found that clathrin is not required for ultrafast endocytosis but is required to generate synaptic vesicles from the endosome. Ultrafast endocytosis fails when actin polymerization is disrupted, or when neurons are stimulated at room temperature instead of physiological temperature. In the absence of ultrafast endocytosis, synaptic vesicles are retrieved directly from the plasma membrane by clathrin-mediated endocytosis. These results may explain discrepancies among published experiments concerning the role of clathrin in synaptic vesicle endocytosis.

Indexed as

AnimalsCell MembraneClathrinEndocytosisEndosomesHumansMiceSynaptic VesiclesTemperatureClathrin

Identifiers

PMID25296249
PMCPMC4291189
OpenAlexW2029980283

What OpenQuestion holds

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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.