Evidence map›Paper›PMID 32195080›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2020

Fibroblast Growth Factor 2-Mediated Regulation of Neuronal Exosome Release Depends on VAMP3/Cellubrevin in Hippocampal Neurons.

Rohit Kumar, Qilin Tang, Stephan A Müller, Pan Gao, Diana Mahlstedt, Sofia Zampagni, Yi Tan, Andreas Klingl, Kai Bötzel, Stefan F Lichtenthaler and 2 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 67 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Rohit KumarDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Qilin TangDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Stephan A MüllerDepartment of Neuroproteomics German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Pan GaoDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Diana MahlstedtDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Sofia ZampagniDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Yi TanDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Andreas KlinglPlant Development and Electron Microscopy Department of Biology I Biocenter Ludwig Maximilian University Großhaderner Str. 2 82152 Planegg-Martinsried Germany.
Kai BötzelDepartment of Neurology Ludwig Maximilian University Marchioninistr. 15 81377 Munich Germany.
Stefan F LichtenthalerDepartment of Neuroproteomics German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Günter U HöglingerDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.
Thomas KoeglspergerDepartment of Translational Neurodegeneration German Centre for Neurodegenerative Diseases Feodor-Lynen-Str. 17 81377 Munich Germany.ORCID https://orcid.org/0000-0001-6101-0323
German Center for Neurodegenerative Diseases · DELudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) are endogenous membrane-derived vesicles that shuttle bioactive molecules between glia and neurons, thereby promoting neuronal survival and plasticity in the central nervous system (CNS) and contributing to neurodegenerative conditions. Although EVs hold great potential as CNS theranostic nanocarriers, the specific molecular factors that regulate neuronal EV uptake and release are currently unknown. A combination of patch-clamp electrophysiology and pH-sensitive dye imaging is used to examine stimulus-evoked EV release in individual neurons in real time. Whereas spontaneous electrical activity and the application of a high-frequency stimulus induce a slow and prolonged fusion of multivesicular bodies (MVBs) with the plasma membrane (PM) in a subset of cells, the neurotrophic factor basic fibroblast growth factor (bFGF) greatly increases the rate of stimulus-evoked MVB-PM fusion events and, consequently, the abundance of EVs in the culture medium. Proteomic analysis of neuronal EVs demonstrates bFGF increases the abundance of the v-SNARE vesicle-associated membrane protein 3 (VAMP3, cellubrevin) on EVs. Conversely, knocking-down VAMP3 in cultured neurons attenuates the effect of bFGF on EV release. The results determine the temporal characteristics of MVB-PM fusion in hippocampal neurons and reveal a new function for bFGF signaling in controlling neuronal EV release.

Indexed as

CD63exosome releasefibroblast growth factormultivesicular bodiespHluorinVAMP3

Identifiers

PMID32195080
PMCPMC7080514
OpenAlexW3004233892

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.