Evidence map›Paper›PMID 33919406›Full record

ArticleInternational journal of molecular sciences2021

Implications of the Wilms' Tumor Suppressor Wt1 in Cardiomyocyte Differentiation.

Nicole Wagner, Marina Ninkov, Ana Vukolic, Günseli Cubukcuoglu Deniz, Minoo Rassoulzadegan, Jean-François Michiels, Kay-Dietrich Wagner

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Cardiomyocyte-Specific Wt1 Is Involved in Cardiac Metabolism and Response to Damage.Journal of cardiovascular development and disease · 2023
    Article
  5. Recapitulating porcine cardiac developmentFrontiers in cell and developmental biology · 2023
    Article
  6. Article
  7. P16INK4A-More Than a Senescence Marker.Life (Basel, Switzerland) · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Transcriptional Regulation of Cardiac Development and Disease.International journal of molecular sciences · 2022
    Article
  12. Article
  13. Every Beat You Take-The Wilms' Tumor Suppressor WT1 and the Heart.International journal of molecular sciences · 2021
    Review
  14. 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

7 authors at 4 institutions in 3 countries.

Nicole WagnerCNRS, INSERM, iBV, Université Côte d'Azur, 06107 Nice, France.ORCID 0000-0002-2746-0707
Marina NinkovCNRS, INSERM, iBV, Université Côte d'Azur, 06107 Nice, France.
Ana VukolicCNRS, INSERM, iBV, Université Côte d'Azur, 06107 Nice, France.
Günseli Cubukcuoglu DenizStem Cell Institute, Ankara University, 06520 Ankara, Turkey.
Minoo RassoulzadeganCNRS, INSERM, iBV, Université Côte d'Azur, 06107 Nice, France.
Jean-François MichielsDepartment of Pathology, CHU Nice, 06107 Nice, France.
Kay-Dietrich WagnerCNRS, INSERM, iBV, Université Côte d'Azur, 06107 Nice, France.ORCID 0000-0001-5483-7760
Centre National de la Recherche Scientifique · FRAnkara University · TRCentre Hospitalier Universitaire de Nice · FRRoche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Wilms' tumor suppressor Wt1 is involved in multiple developmental processes and adult tissue homeostasis. The first phenotypes recognized in Wt1 knockout mice were developmental cardiac and kidney defects. Wt1 expression in the heart has been described in epicardial, endothelial, smooth muscle cells, and fibroblasts. Expression of Wt1 in cardiomyocytes has been suggested but remained a controversial issue, as well as the role of Wt1 in cardiomyocyte development and regeneration after injury. We determined cardiac Wt1 expression during embryonic development, in the adult, and after cardiac injury by quantitative RT-PCR and immunohistochemistry. As in vitro model, phenotypic cardiomyocyte differentiation, i.e., the appearance of rhythmically beating clones from mouse embryonic stem cells (mESCs) and associated changes in gene expression were analyzed. We detected Wt1 in cardiomyocytes from embryonic day (E10.5), the first time point investigated, until adult age. Cardiac Wt1 mRNA levels decreased during embryonic development. In the adult, Wt1 was reactivated in cardiomyocytes 48 h and 3 weeks following myocardial infarction. Wt1 mRNA levels were increased in differentiating mESCs. Overexpression of Wt1(-KTS) and Wt1(+KTS) isoforms in ES cells reduced the fraction of phenotypically cardiomyocyte differentiated clones, which was preceded by a temporary increase in c-kit expression in Wt1(-KTS) transfected ES cell clones and induction of some cardiomyocyte markers. Taken together, Wt1 shows a dynamic expression pattern during cardiomyocyte differentiation and overexpression in ES cells reduces their phenotypical cardiomyocyte differentiation.

Indexed as

Cell DifferentiationAnimalsFemaleMiceMouse Embryonic Stem CellsMyocardial InfarctionMyocytes, CardiacWT1 ProteinsWT1 Proteinscardiomyocyte differentiationmouse embryonic stem cellsmyocardial infarctionWilms’ tumor suppressor 1

Identifiers

PMID33919406
PMCPMC8122684
OpenAlexW3153366383

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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 OpenQuestion graph.