Evidence map›Paper›PMID 36351828›Full record

ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2022

Super-Resolution Microscopy Opens New Doors to Life at the Nanoscale.

Martin Fuhrmann, Nala Gockel, Misa Arizono, Yulia Dembitskaya, U Valentin Nägerl, Francesca Pennacchietti, Martina Damenti, Ilaria Testa, Katrin I Willig

Abstract readReview
In one paragraph

Review in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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  11. Novel Techniques for Mapping DNA Damage and Repair in the Brain.International journal of molecular sciences · 2024
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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.

Martin FuhrmannGerman Center for Neurodegenerative Diseases, Neuroimmunology and Imaging Group, Bonn, Germany, 53127 kwillig@mpinat.mpg.de testa@kth.se martin.fuhrmann@dzne.de valentin.nagerl@u-bordeaux.fr.ORCID 0000-0001-7672-2913
Nala GockelGerman Center for Neurodegenerative Diseases, Neuroimmunology and Imaging Group, Bonn, Germany, 53127.
Misa ArizonoSynaptic Plasticity and Super-Resolution Microscopy Group, Institut Interdisciplinaire de Neurosciences, Université de Bordeaux/Centre National de la Recherche Scientifique Unité Mixte de Recherche 5297, Bordeaux, France, 33076.
Yulia DembitskayaSynaptic Plasticity and Super-Resolution Microscopy Group, Institut Interdisciplinaire de Neurosciences, Université de Bordeaux/Centre National de la Recherche Scientifique Unité Mixte de Recherche 5297, Bordeaux, France, 33076.ORCID 0000-0002-6680-4242
U Valentin NägerlSynaptic Plasticity and Super-Resolution Microscopy Group, Institut Interdisciplinaire de Neurosciences, Université de Bordeaux/Centre National de la Recherche Scientifique Unité Mixte de Recherche 5297, Bordeaux, France, 33076 kwillig@mpinat.mpg.de testa@kth.se martin.fuhrmann@dzne.de valentin.nagerl@u-bordeaux.fr.
Francesca PennacchiettiDepartment of Applied Physics and Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, 100 44, Sweden.
Martina DamentiDepartment of Applied Physics and Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, 100 44, Sweden.ORCID 0000-0002-4209-5381
Ilaria TestaDepartment of Applied Physics and Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, 100 44, Sweden kwillig@mpinat.mpg.de testa@kth.se martin.fuhrmann@dzne.de valentin.nagerl@u-bordeaux.fr.
Katrin I WilligGroup of Optical Nanoscopy in Neuroscience, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany, 37075 kwillig@mpinat.mpg.de testa@kth.se martin.fuhrmann@dzne.de valentin.nagerl@u-bordeaux.fr.ORCID 0000-0002-1860-334X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Super-resolution fluorescence microscopy holds tremendous potential for discovery in neuroscience. Much of the molecular machinery and anatomic specializations that give rise to the unique and bewildering electrochemical activity of neurons are nanoscale by design, ranging somewhere between 1 nm and 1 μm. It is at this scale where most of the unknown and exciting action is and where cell biologists flock to in their dreams, but it was off limits for light microscopy until recently. While the optical principles of super-resolution microscopy are firmly established by now, the technology continues to advance rapidly in many crucial areas, enhancing its performance and reliability, and making it more accessible and user-friendly, which is sorely needed. Indeed, super-resolution microscopy techniques are nowadays widely used for visualizing immunolabeled protein distributions in fixed or living cells. However, a great potential of super-resolution microscopy for neuroscience lies in shining light on the nanoscale structures and biochemical activities in live-tissue settings, which should be developed and harnessed much more fully. In this review, we will present several vivid examples based on STED and RESOLFT super-resolution microscopy, illustrating the possibilities and challenges of nano-imaging

Indexed as

NeuronsMicroscopy, FluorescenceReproducibility of Resultsactindendritic spinesimagingin vivomicrogliaRESOLFTSTEDsuper-resolutionSUSHIsynapsetwo-photon

Identifiers

PMID36351828
PMCPMC9665916

What OpenQuestion holds

Textmetadata
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.