Evidence map›Paper›PMID 34149361›Full record

ArticleFrontiers in cellular neuroscience2021

Heterogeneity and Development of Fine Astrocyte Morphology Captured by Diffraction-Limited Microscopy.

Daniel Minge, Cátia Domingos, Petr Unichenko, Charlotte Behringer, Alberto Pauletti, Stefanie Anders, Michel K Herde, Andrea Delekate, Polina Gulakova, Susanne Schoch and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

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  8. Super-resolution Analysis of Astrocyte Morphology Using Expansion Microscopy.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  9. Astrocytic transcriptional and epigenetic mechanisms of drug addiction.Journal of neural transmission (Vienna, Austria : 1996) · 2024
    Review
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  12. Astrocyte β-Adrenergic Receptor Activity Regulates NMDA Receptor Signaling of Medial Prefrontal Cortex Pyramidal Neurons.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

12 authors at 4 institutions in 2 countries.

Daniel MingeInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Cátia DomingosInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Petr UnichenkoInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Charlotte BehringerInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Alberto PaulettiInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Stefanie AndersInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Michel K HerdeInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
Andrea DelekateGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Polina GulakovaDepartment of Neuropathology, University Hospital Bonn, Bonn, Germany.
Susanne SchochDepartment of Neuropathology, University Hospital Bonn, Bonn, Germany.
Gabor C PetzoldGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Christian HennebergerInstitute of Cellular Neurosciences, Medical Faculty, University of Bonn, Bonn, Germany.
University of Bonn · DEGerman Center for Neurodegenerative Diseases · DEUniversity Hospital Bonn · DEUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fine processes of single astrocytes can contact many thousands of synapses whose function they can modulate through bi-directional signaling. The spatial arrangement of astrocytic processes and neuronal structures is relevant for such interactions and for the support of neuronal signaling by astrocytes. At the same time, the geometry of perisynaptic astrocyte processes is variable and dynamically regulated. Studying these fine astrocyte processes represents a technical challenge, because many of them cannot be fully resolved by diffraction-limited microscopy. Therefore, we have established two indirect parameters of astrocyte morphology, which, while not fully resolving local geometry by design, provide statistical measures of astrocyte morphology: the fraction of tissue volume that astrocytes occupy and the density of resolvable astrocytic processes. Both are straightforward to obtain using widely available microscopy techniques. We here present the approach and demonstrate its robustness across various experimental conditions using mainly two-photon excitation fluorescence microscopy in acute slices and

Indexed as

analysisastrocytesdevelopmentheterogeneitymicroscopymorphologyperisynaptic processes of astrocytes

Identifiers

PMID34149361
PMCPMC8211899
OpenAlexW3168634597

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.