Evidence map›Paper›PMID 25650918›Full record

ArticleBiophysical journal2015

Three-dimensional structure of the intercalated disc reveals plicate domain and gap junction remodeling in heart failure.

Christian Pinali, Hayley J Bennett, J Bernard Davenport, Jessica L Caldwell, Tobias Starborg, Andrew W Trafford, Ashraf Kitmitto

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

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  10. Localization of NaThe Journal of physiology · 2021
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  16. Cardiomyocyte damage control in heart failure and the role of the sarcolemma.Journal of muscle research and cell motility · 2019
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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

7 authors at 1 institution in 2 countries.

Christian PinaliInstitute of Cardiovascular Sciences, Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
Hayley J BennettInstitute of Cardiovascular Sciences, Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
J Bernard DavenportInstitute of Cardiovascular Sciences, Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
Jessica L CaldwellInstitute of Cardiovascular Sciences, Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
Tobias StarborgFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Andrew W TraffordInstitute of Cardiovascular Sciences, Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
Ashraf KitmittoInstitute of Cardiovascular Sciences, Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom. Electronic address: ashraf.kitmitto@manchester.ac.uk.
University of Manchester · GB

Funding

British Heart Foundation FS/12/57/29717British Heart Foundation RG/11/2/28701Wellcome Trust 088785Wellcome Trust 088785/Z/09/Z
6 · The paper itself

Abstract

The intercalated disc (ICD) orchestrates electrochemical and mechanical communication between neighboring cardiac myocytes, properties that are perturbed in heart failure (HF). Although structural data from transmission electron microscopy two-dimensional images have provided valuable insights into the domains forming the ICD, there are currently no three-dimensional (3D) reconstructions for an entire ICD in healthy or diseased hearts. Here, we aimed to understand the link between changes in protein expression in an ovine tachypacing-induced HF model and ultrastructural remodeling of the ICD by determining the 3D intercalated disc architecture using serial block face scanning electron microscopy. In the failing myocardium there is no change to the number of ICDs within the left ventricle, but there is an almost doubling of the number of discs with a surface area of <1.0 × 10(8)μm(2) in comparison to control. The 3D reconstructions further revealed that there is remodeling of the plicate domains and gap junctions with vacuole formation around and between the contributing membranes that form the ICDs in HF. Biochemical analysis revealed upregulation of proteins involved in stabilizing the adhesive and mechanical properties consistent with the morphological changes. Our studies here have shown that in tachypacing-induced HF mechanical stresses are associated with both structural and molecular alterations. To our knowledge, these data together provide novel, to our knowledge, insights as to how remodeling at the molecular and structural levels leads to impaired intercellular communication.

Indexed as

Imaging, Three-DimensionalAnimalsGap JunctionsHeart FailureHeart VentriclesIntercellular JunctionsMitochondria, HeartProteinsSheepUp-RegulationVacuolesProteins

Identifiers

PMID25650918
PMCPMC4317535
OpenAlexW2098534133

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.