Evidence map›Paper›PMID 39202712›Full record

ArticleLife (Basel, Switzerland)2024

A Proof of Principle 2D Spatial Proteome Mapping Analysis Reveals Distinct Regional Differences in the Cardiac Proteome.

Wendy E Heywood, Jon Searle, Richard Collis, Ivan Doykov, Michael Ashworth, Neil Sebire, Andrew Bamber, Mathias Gautel, Simon Eaton, Caroline J Coats and 2 more

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Wendy E HeywoodUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.
Jon SearleUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.
Richard CollisInstitute of Cardiovascular Science, University College London, Gower Street, London WC1E 6BT, UK.
Ivan DoykovUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.
Michael AshworthHistopathology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 1EH, UK.
Neil SebireHistopathology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 1EH, UK.
Andrew BamberHistopathology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 1EH, UK.
Mathias GautelRandall Division of Cell and Molecular Biophysics, Muscle Signalling Section, King's College, London WC2E 2LS, UK.ORCID 0000-0003-4027-9803
Simon EatonUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.ORCID 0000-0003-0892-9204
Caroline J CoatsInstitute of Cardiovascular Science, University College London, Gower Street, London WC1E 6BT, UK.ORCID 0000-0002-3208-470X
Perry M ElliottInstitute of Cardiovascular Science, University College London, Gower Street, London WC1E 6BT, UK.ORCID 0000-0003-3383-3984
Kevin MillsUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.ORCID 0000-0003-0763-8288

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteomics studies often explore phenotypic differences between whole organs and systems. Within the heart, more subtle variation exists. To date, differences in the underlying proteome are only described between whole cardiac chambers. This study, using the bovine heart as a model, investigates inter-regional differences and assesses the feasibility of measuring detailed, cross-tissue variance in the cardiac proteome. Using a bovine heart, we created a two-dimensional section through a plane going through two chambers. This plane was further sectioned into 4 × 4 mm cubes and analysed using label-free proteomics. We identified three distinct proteomes. When mapped to the extracted sections, the proteomes corresponded largely to the outer wall of the right ventricle and secondly to the outer wall of the left ventricle, right atrial appendage, tricuspid and mitral valves, modulator band, and parts of the left atrium. The third separate proteome corresponded to the inner walls of the left and right ventricles, septum, and left atrial appendage. Differential protein abundancies indicated differences in energy metabolism between regions. Data analyses of the mitochondrial proteins revealed a variable pattern of abundances of complexes I-V between the proteomes, indicating differences in the bioenergetics of the different cardiac sub-proteomes. Mapping of disease-associated proteins interestingly showed desmoglein-2, for which defects in this protein are known to cause Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy, which was present predominantly in the outer wall of the left ventricle. This study highlights that organs can have variable proteomes that do not necessarily correspond to anatomical features.

Indexed as

desmoglein-2heartmitochondriaproteomeproteomics

Identifiers

PMID39202712
PMCPMC11355120

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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.