Evidence map›Paper›PMID 32492970›Full record

ArticleCells2020

Comparison of Multiscale Imaging Methods for Brain Research.

Jessica Tröger, Christian Hoischen, Birgit Perner, Shamci Monajembashi, Aurélien Barbotin, Anna Löschberger, Christian Eggeling, Michael M Kessels, Britta Qualmann, Peter Hemmerich

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.9field-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

8 citing papers in PubMed, 15 citations in OpenAlex.

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  8. Comparing Super-Resolution Microscopy Techniques to Analyze Chromosomes.International journal of molecular sciences · 2021
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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 5 institutions in 2 countries.

Jessica TrögerInstitute of Biochemistry I, Jena University Hospital-Friedrich Schiller University Jena, Nonnenplan 2-4, 07743 Jena, Germany.
Christian HoischenCore Facility Imaging, Leibniz Institute on Aging-Fritz Lipmann Institute (FLI), Beutenbergstraße 11, 07745 Jena, Germany.
Birgit PernerCore Facility Imaging, Leibniz Institute on Aging-Fritz Lipmann Institute (FLI), Beutenbergstraße 11, 07745 Jena, Germany.
Shamci MonajembashiCore Facility Imaging, Leibniz Institute on Aging-Fritz Lipmann Institute (FLI), Beutenbergstraße 11, 07745 Jena, Germany.
Aurélien BarbotinDepartment of Engineering Science, University of Oxford, Parks Road, Oxford OX13PJ, UK.
Anna LöschbergerAdvanced Development Light Microscopy, Carl Zeiss Microscopy GmbH, Carl-Zeiss-Promenade 10, 07745 Jena, Germany.
Christian EggelingMRC Human Immunology Unit & Wolfson Imaging Center Oxford, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX39DS, UK.
Michael M KesselsInstitute of Biochemistry I, Jena University Hospital-Friedrich Schiller University Jena, Nonnenplan 2-4, 07743 Jena, Germany.
Britta QualmannInstitute of Biochemistry I, Jena University Hospital-Friedrich Schiller University Jena, Nonnenplan 2-4, 07743 Jena, Germany.
Peter HemmerichCore Facility Imaging, Leibniz Institute on Aging-Fritz Lipmann Institute (FLI), Beutenbergstraße 11, 07745 Jena, Germany.
Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEJena University Hospital · DECarl Zeiss (Germany) · DELeibniz Institute of Photonic Technology · DEUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council G0902418Medical Research Council MC_UU_00008/9Medical Research Council MC_UU_12010Medical Research Council MC_UU_12010/9Medical Research Council MC_UU_12025Medical Research Council MR/K01577X/1Wellcome Trust 098274/Z/12/ZWellcome Trust 100262Z/12/ZWellcome Trust 104924/14/Z/14Wellcome Trust 107457/Z/15/Z
6 · The paper itself

Abstract

A major challenge in neuroscience is how to study structural alterations in the brain. Even small changes in synaptic composition could have severe outcomes for body functions. Many neuropathological diseases are attributable to disorganization of particular synaptic proteins. Yet, to detect and comprehensively describe and evaluate such often rather subtle deviations from the normal physiological status in a detailed and quantitative manner is very challenging. Here, we have compared side-by-side several commercially available light microscopes for their suitability in visualizing synaptic components in larger parts of the brain at low resolution, at extended resolution as well as at super-resolution. Microscopic technologies included stereo, widefield, deconvolution, confocal, and super-resolution set-ups. We also analyzed the impact of adaptive optics, a motorized objective correction collar and CUDA graphics card technology on imaging quality and acquisition speed. Our observations evaluate a basic set of techniques, which allow for multi-color brain imaging from centimeter to nanometer scales. The comparative multi-modal strategy we established can be used as a guide for researchers to select the most appropriate light microscopy method in addressing specific questions in brain research, and we also give insights into recent developments such as optical aberration corrections.

Indexed as

Imaging, Three-DimensionalResearchAnimalsBrainMaleMiceMicroscopy, ConfocalNeuronsRatsSingle-Cell AnalysisSynapsesadvanced light microscopybrainmulti-scale imagingsuper-resolutiontissue

Identifiers

PMID32492970
PMCPMC7349602
OpenAlexW3030973966

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.