Evidence map›Paper›PMID 36535932›Full record

ArticleNature communications2022

Rapid and reversible optogenetic silencing of synaptic transmission by clustering of synaptic vesicles.

Dennis Vettkötter, Martin Schneider, Brady D Goulden, Holger Dill, Jana Liewald, Sandra Zeiler, Julia Guldan, Yilmaz Arda Ateş, Shigeki Watanabe, Alexander Gottschalk

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

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  12. RIM and RIM-Binding Protein Localize Synaptic CaV2 Channels to Differentially Regulate Transmission in Neuronal Circuits.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
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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

10 authors at 2 institutions in 2 countries.

Dennis VettkötterBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.
Martin SchneiderBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.ORCID 0000-0001-9760-6292
Brady D GouldenDepartment of Cell Biology and Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, MD, 21205, USA.
Holger DillBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.
Jana LiewaldBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.ORCID 0000-0002-2050-0745
Sandra ZeilerBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.
Julia GuldanBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.
Yilmaz Arda AteşBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany.
Shigeki WatanabeDepartment of Cell Biology and Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, MD, 21205, USA.ORCID 0000-0001-7580-8141
Alexander GottschalkBuchmann Institute for Molecular Life Sciences, Goethe University, D-60438, Frankfurt, Germany. a.gottschalk@em.uni-frankfurt.de.ORCID 0000-0002-1197-6119
Goethe University Frankfurt · DEJohns Hopkins University · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Reviving electron microscopy for synaptic cell biologyDP2NS111133 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WATANABE, SHIGEKI · 2018 to 2018
$2.5M
Spatial and molecular determinants of fusion probability and timingR01NS105810 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WATANABE, SHIGEKI · 2018 to 2022
$1.8M
NIH HHS P40 OD010440NINDS NIH HHS DP2 NS111133NINDS NIH HHS R01 NS105810
6 · The paper itself

Abstract

Acutely silencing specific neurons informs about their functional roles in circuits and behavior. Existing optogenetic silencers include ion pumps, channels, metabotropic receptors, and tools that damage the neurotransmitter release machinery. While the former hyperpolarize the cell, alter ionic gradients or cellular biochemistry, the latter allow only slow recovery, requiring de novo synthesis. Thus, tools combining fast activation and reversibility are needed. Here, we use light-evoked homo-oligomerization of cryptochrome CRY2 to silence synaptic transmission, by clustering synaptic vesicles (SVs). We benchmark this tool, optoSynC, in Caenorhabditis elegans, zebrafish, and murine hippocampal neurons. optoSynC clusters SVs, observable by electron microscopy. Locomotion silencing occurs with tau

Indexed as

OptogeneticsSynaptic VesiclesAnimalsCaenorhabditis elegansCluster AnalysisMiceSynaptic TransmissionZebrafish

Identifiers

PMID36535932
PMCPMC9763335
OpenAlexW4313340035

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.