Evidence map›Paper›PMID 28211501›Full record

ArticleScientific reports2017

High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis.

Maxence Frétaud, Laurie Rivière, Élodie De Job, Stéphanie Gay, Jean-Jacques Lareyre, Jean-Stéphane Joly, Pierre Affaticati, Violette Thermes

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. T-CLEARE: a pilot community-driven tissue clearing protocol repository.Frontiers in bioengineering and biotechnology · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Three-Dimensional Imaging in Stem Cell-Based Researches.Frontiers in veterinary science · 2021
    Review
  9. Tissue Optical Clearing for Biomedical Imaging: From In Vitro to In Vivo.Advances in experimental medicine and biology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
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

8 authors.

Maxence FrétaudINRA, UR1037 Fish Physiology and Genomics, F-35000 Rennes, France.
Laurie RivièreTefor Core Facility, Paris-Saclay Institute of Neuroscience, CNRS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Élodie De JobTefor Core Facility, Paris-Saclay Institute of Neuroscience, CNRS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Stéphanie GayINRA, UR1037 Fish Physiology and Genomics, F-35000 Rennes, France.
Jean-Jacques LareyreINRA, UR1037 Fish Physiology and Genomics, F-35000 Rennes, France.
Jean-Stéphane JolyTefor Core Facility, Paris-Saclay Institute of Neuroscience, CNRS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Pierre AffaticatiTefor Core Facility, Paris-Saclay Institute of Neuroscience, CNRS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Violette ThermesINRA, UR1037 Fish Physiology and Genomics, F-35000 Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zebrafish testis has become a powerful model for reproductive biology of teleostean fishes and other vertebrates and encompasses multiple applications in applied and basic research. Many studies have focused on 2D images, which is time consuming and implies extrapolation of results. Three-dimensional imaging of whole organs recently became an important challenge to better understand their architecture and allow cell enumeration. Several protocols have thus been developed to enhance sample transparency, a limiting step for imaging large biological samples. However, none of these methods has been applied to the zebrafish testis. We tested five clearing protocols to determine if some of them could be applied with only small modifications to the testis. We compared clearing efficiency at both macroscopic and microscopic levels. CUBIC and PACT were suitable for an efficient transparency, an optimal optical penetration, the GFP fluorescence preservation and avoiding meaningful tissue deformation. Finally, we succeeded in whole testis 3D capture at a cellular resolution with both CUBIC and PACT, which will be valuable in a standard workflow to investigate the 3D architecture of the testis and its cellular content. This paves the way for further development of high content phenotyping studies in several fields including development, genetic or toxicology.

Indexed as

Imaging, Three-DimensionalAnimalsAnimals, Genetically ModifiedMaleMicroscopy, Fluorescence, MultiphotonOptical ImagingTestisZebrafish

Identifiers

PMID28211501
PMCPMC5314416

What OpenQuestion holds

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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.