Evidence map›Paper›PMID 29508067›Full record

ArticleHistochemistry and cell biology2018

Three-dimensional reconstruction of the intercalated disc including the intercellular junctions by applying volume scanning electron microscopy.

Bieke Vanslembrouck, Anna Kremer, Benjamin Pavie, Frans van Roy, Saskia Lippens, Jolanda van Hengel

Abstract read
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In one paragraph

Article in Histochemistry and cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The desmosome comes into focus.The Journal of cell biology · 2024
    Review
  5. Indirect Correlative Light and Electron Microscopy (iCLEM): A Novel Pipeline for Multiscale Quantification of Structure From Molecules to Organs.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Localization of NaThe Journal of physiology · 2021
    Article
  11. Article
  12. Article
  13. In focus in HCB.Histochemistry and cell biology · 2020
    Article
  14. Article
  15. In focus in HCB.Histochemistry and cell biology · 2018
    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

6 authors at 2 institutions in 1 country.

Bieke VanslembrouckDepartment of Basic Medical Science, Faculty of Medicine and Health Sciences, Ghent University, Corneel Heymanslaan 10, Building B, 9000, Ghent, Belgium.
Anna KremerVIB BioImaging Core, Ghent, Belgium.
Benjamin PavieVIB BioImaging Core, Ghent, Belgium.
Frans van RoyVIB Center for Inflammation Research, Ghent, Belgium.
Saskia LippensVIB BioImaging Core, Ghent, Belgium.
Jolanda van HengelDepartment of Basic Medical Science, Faculty of Medicine and Health Sciences, Ghent University, Corneel Heymanslaan 10, Building B, 9000, Ghent, Belgium. Jolanda.vanhengel@ugent.be.ORCID http://orcid.org/0000-0003-0645-0435
Ghent University · BEVIB-UGent Center for Inflammation Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intercalated disc (ID) contains different kinds of intercellular junctions: gap junctions (GJs), desmosomes and areae compositae, essential for adhesion and communication between adjacent cardiomyocytes. The junctions can be identified based on their morphology when imaged using transmission electron microscopy (TEM), however, only with very limited information in the z-dimension. The application of volume EM techniques can give insight into the three-dimensional (3-D) organization of complex biological structures. In this study, we generated 3-D datasets using serial block-face scanning electron microscopy (SBF-SEM) and focused ion beam SEM (FIB-SEM), the latter resulting in datasets with 5 nm isotropic voxels. We visualized cardiomyocytes in murine ventricular heart tissue and, for the first time, we could three-dimensionally reconstruct the ID including desmosomes and GJs with 5 nm precision in a large volume. Results show in three dimensions a highly folded structure of the ID, with the presence of GJs and desmosomes in both plicae and interplicae regions. We observed close contact of GJs with mitochondria and a variable spatial distribution of the junctions. Based on measurements of the shape of the intercellular junctions in 3-D, it is seen that GJs and desmosomes vary in size, depending on the region within the ID. This demonstrates that volume EM is essential to visualize morphological changes and its potential to quantitatively determine structural changes between normal and pathological conditions, e.g., cardiomyopathies.

Indexed as

Imaging, Three-DimensionalAnimalsIntercellular JunctionsMiceMicroscopy, Electron, ScanningMyocytes, CardiacPhenotypeCardiac intercalated discCardiomyocytesDesmosomeGap junctionVolume electron microscopy

Identifiers

PMID29508067
OpenAlexW2791444715

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.