Evidence map›Paper›PMID 38057295›Full record

ArticleCell death discovery2023

A novel DSP zebrafish model reveals training- and drug-induced modulation of arrhythmogenic cardiomyopathy phenotypes.

Rudy Celeghin, Giovanni Risato, Giorgia Beffagna, Marco Cason, Maria Bueno Marinas, Mila Della Barbera, Nicola Facchinello, Alice Giuliodori, Raquel Brañas Casas, Micol Caichiolo and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
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

19 authors at 4 institutions in 2 countries.

Rudy Celeghin *Department of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.ORCID http://orcid.org/0000-0001-9047-9032
Giovanni Risato *Department of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Giorgia BeffagnaDepartment of Biology, University of Padova, Padova, 35131, Italy. giorgia.beffagna@gmail.com.
Marco CasonDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Maria Bueno MarinasDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Mila Della BarberaDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Nicola FacchinelloNeuroscience Institute, Italian National Research Council (CNR), Padova, 35131, Italy.ORCID http://orcid.org/0000-0003-1682-3696
Alice GiuliodoriDepartment of Biology, University of Padova, Padova, 35131, Italy.
Raquel Brañas CasasDepartment of Biology, University of Padova, Padova, 35131, Italy.
Micol CaichioloDepartment of Biology, University of Padova, Padova, 35131, Italy.ORCID http://orcid.org/0000-0002-9941-0231
Andrea VettoriDepartment of Biotechnology, University of Verona, Verona, 37134, Italy.ORCID http://orcid.org/0000-0003-4958-0619
Enrico GrisanSchool of Engineering, London South Bank University, London, SE1 0AA, UK.
Stefania RizzoDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Luisa Dalla ValleDepartment of Biology, University of Padova, Padova, 35131, Italy.ORCID http://orcid.org/0000-0001-8097-6369
Francesco ArgentonDepartment of Biology, University of Padova, Padova, 35131, Italy.ORCID http://orcid.org/0000-0002-0803-8236
Gaetano ThieneDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.ORCID http://orcid.org/0000-0002-8814-2577
Natascia TisoDepartment of Biology, University of Padova, Padova, 35131, Italy. natascia.tiso@unipd.it.ORCID http://orcid.org/0000-0002-5444-9853
Kalliopi PilichouDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Cristina BassoDepartment of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy. cristina.basso@unipd.it.ORCID http://orcid.org/0000-0002-0195-9753
University of Padua · ITLondon South Bank University · GBNeuroscience Institute · ITUniversity of Verona · IT

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) IG-2017-19928Fondazione Cassa di Risparmio di Padova e Rovigo (Foundation Cariparo) grant SHoCDFondazione Telethon (Telethon Foundation) GGP19287Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research) PNRR M4C2 CN00000041
6 · The paper itself

Abstract

Arrhythmogenic cardiomyopathy (AC) is an inherited disorder characterized by progressive loss of the ventricular myocardium causing life-threatening ventricular arrhythmias, syncope and sudden cardiac death in young and athletes. About 40% of AC cases carry one or more mutations in genes encoding for desmosomal proteins, including Desmoplakin (Dsp). We present here the first stable Dsp knock-out (KO) zebrafish line able to model cardiac alterations and cell signalling dysregulation, characteristic of the AC disease, on which environmental factors and candidate drugs can be tested. Our stable Dsp knock-out (KO) zebrafish line was characterized by cardiac alterations, oedema and bradycardia at larval stages. Histological analysis of mutated adult hearts showed reduced contractile structures and abnormal shape of the ventricle, with thinning of the myocardial layer, vessels dilation and presence of adipocytes within the myocardium. Moreover, TEM analysis revealed "pale", disorganized and delocalized desmosomes. Intensive physical training protocol caused a global worsening of the cardiac phenotype, accelerating the progression of the disease. Of note, we detected a decrease of Wnt/β-catenin signalling, recently associated with AC pathogenesis, as well as Hippo/YAP-TAZ and TGF-β pathway dysregulation. Pharmacological treatment of mutated larvae with SB216763, a Wnt/β-catenin agonist, rescued pathway expression and cardiac abnormalities, stabilizing the heart rhythm. Overall, our Dsp KO zebrafish line recapitulates many AC features observed in human patients, pointing at zebrafish as a suitable system for in vivo analysis of environmental modulators, such as the physical exercise, and the screening of pathway-targeted drugs, especially related to the Wnt/β-catenin signalling cascade.

Identifiers

PMID38057295
PMCPMC10700616
OpenAlexW4389389608

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.