Evidence map›Paper›PMID 36670288›Full record

ArticleBasic research in cardiology2023

Monoamine oxidase A-dependent ROS formation modulates human cardiomyocyte differentiation through AKT and WNT activation.

Moises Di Sante, Salvatore Antonucci, Laura Pontarollo, Ilaria Cappellaro, Francesca Segat, Soni Deshwal, Elisa Greotti, Luis F Grilo, Roberta Menabò, Fabio Di Lisa and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Basic research in cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

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  12. The role of β-catenin in cardiac diseases.Frontiers in pharmacology · 2023
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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

11 authors at 3 institutions in 3 countries.

Moises Di SanteDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy.
Salvatore AntonucciDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy.
Laura PontarolloDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy.
Ilaria CappellaroDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy.
Francesca SegatDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy.
Soni DeshwalDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy.
Elisa GreottiNeuroscience Institute, National Research Council of Italy (CNR), Via Ugo Bassi 58/B, 35131, Padua, Italy.
Luis F GriloCenter for Neuroscience and Cell Biology, University of Coimbra, 3004-504, Coimbra, Portugal.
Roberta MenabòNeuroscience Institute, National Research Council of Italy (CNR), Via Ugo Bassi 58/B, 35131, Padua, Italy.
Fabio Di LisaDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy. fabio.dilisa@unipd.it.
Nina KaludercicDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131, Padua, Italy. nina.kaludercic@unipd.it.ORCID http://orcid.org/0000-0002-8447-6246
University of Padua · ITNeuroscience Institute · ITUniversity of Coimbra · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During embryonic development, cardiomyocytes undergo differentiation and maturation, processes that are tightly regulated by tissue-specific signaling cascades. Although redox signaling pathways involved in cardiomyogenesis are established, the exact sources responsible for reactive oxygen species (ROS) formation remain elusive. The present study investigates whether ROS produced by the mitochondrial flavoenzyme monoamine oxidase A (MAO-A) play a role in cardiomyocyte differentiation from human induced pluripotent stem cells (hiPSCs). Wild type (WT) and MAO-A knock out (KO) hiPSCs were generated by CRISPR/Cas9 genome editing and subjected to cardiomyocyte differentiation. Mitochondrial ROS levels were lower in MAO-A KO compared to the WT cells throughout the differentiation process. MAO-A KO hiPSC-derived cardiomyocytes (hiPSC-CMs) displayed sarcomere disarray, reduced α- to β-myosin heavy chain ratio, GATA4 upregulation and lower macroautophagy levels. Functionally, genetic ablation of MAO-A negatively affected intracellular Ca

Indexed as

Induced Pluripotent Stem CellsMyocytes, CardiacCell DifferentiationHumansMonoamine OxidaseProto-Oncogene Proteins c-aktReactive Oxygen SpeciesWnt Signaling PathwayMonoamine OxidaseProto-Oncogene Proteins c-aktReactive Oxygen SpeciesCardiomyocyte differentiationCell fateDevelopmenthiPSCsReactive oxygen species

Identifiers

PMID36670288
PMCPMC9859871
OpenAlexW4317555809

What OpenQuestion holds

Textmetadata
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.