Evidence map›Paper›PMID 30988508›Full record

ArticleNature protocols2019

High-speed imaging of glutamate release with genetically encoded sensors.

Céline D Dürst, J Simon Wiegert, Nordine Helassa, Silke Kerruth, Catherine Coates, Christian Schulze, Michael A Geeves, Katalin Török, Thomas G Oertner

Abstract read
In one paragraph

Article in Nature protocols, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
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  6. Optical analysis of glutamate spread in the neuropil.Cerebral cortex (New York, N.Y. : 1991) · 2022
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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

9 authors.

Céline D DürstInstitute for Synaptic Physiology, Center for Molecular Neurobiology Hamburg, Hamburg, Germany.
J Simon WiegertInstitute for Synaptic Physiology, Center for Molecular Neurobiology Hamburg, Hamburg, Germany.ORCID http://orcid.org/0000-0003-0893-9349
Nordine HelassaMolecular and Clinical Sciences Research Institute, St George's, University of London, London, UK.ORCID http://orcid.org/0000-0003-3743-1886
Silke KerruthMolecular and Clinical Sciences Research Institute, St George's, University of London, London, UK.
Catherine CoatesMolecular and Clinical Sciences Research Institute, St George's, University of London, London, UK.
Christian SchulzeInstitute for Synaptic Physiology, Center for Molecular Neurobiology Hamburg, Hamburg, Germany.
Michael A GeevesSchool of Biosciences, University of Kent, Canterbury, UK.ORCID http://orcid.org/0000-0002-9364-8898
Katalin TörökMolecular and Clinical Sciences Research Institute, St George's, University of London, London, UK.
Thomas G OertnerInstitute for Synaptic Physiology, Center for Molecular Neurobiology Hamburg, Hamburg, Germany. thomas.oertner@zmnh.uni-hamburg.de.ORCID http://orcid.org/0000-0002-2312-7528

Funding

European Research Council 714762
6 · The paper itself

Abstract

The strength of an excitatory synapse depends on its ability to release glutamate and on the density of postsynaptic receptors. Genetically encoded glutamate indicators (GEGIs) allow eavesdropping on synaptic transmission at the level of cleft glutamate to investigate properties of the release machinery in detail. Based on the sensor iGluSnFR, we recently developed accelerated versions of GEGIs that allow investigation of synaptic release during 100-Hz trains. Here, we describe the detailed procedures for design and characterization of fast iGluSnFR variants in vitro, transfection of pyramidal cells in organotypic hippocampal cultures, and imaging of evoked glutamate transients with two-photon laser-scanning microscopy. As the released glutamate spreads from a point source-the fusing vesicle-it is possible to localize the vesicle fusion site with a precision exceeding the optical resolution of the microscope. By using a spiral scan path, the temporal resolution can be increased to 1 kHz to capture the peak amplitude of fast iGluSnFR transients. The typical time frame for these experiments is 30 min per synapse.

Indexed as

Biosensing TechniquesCA3 Region, HippocampalCells, CulturedGlutamic AcidHumansMicroscopy, ConfocalMolecular ProbesOptical ImagingSynaptic TransmissionTransfectionGlutamic AcidMolecular Probes

Identifiers

PMID30988508
PMCPMC6751072

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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.