Evidence map›Paper›PMID 23144723›Full record

ArticlePloS one2012

Cardiac gene activation analysis in mammalian non-myoblasic cells by Nkx2-5, Tbx5, Gata4 and Myocd.

Lei Zhou, Yu Liu, Li Lu, Xinzheng Lu, Richard A F Dixon

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Direct Cardiac Cellular Reprogramming for Cardiac Regeneration.Current treatment options in cardiovascular medicine · 2016
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 4 institutions in 2 countries.

Lei ZhouDepartment of Molecular Cardiology, Texas Heart Institute, Houston, Texas, United States of America. Lzhou@heart.thi.tmc.edu
Yu Liu
Li Lu
Xinzheng Lu
Richard A F Dixon
Heart Foundation · USNanjing Medical University · CNThe University of Texas MD Anderson Cancer Center · USUniversity of Houston · US

Funding

Prostacyclin-secreting Cells as Therapy for Pulmonary Artery HypertensionRC1HL100807 · NHLBI · TEXAS HEART INSTITUTE · PI DIXON, RICHARD A.F., RUAN, KE-HE · 2009 to 2010
$1.0M
NHLBI NIH HHS RC1 HL100807
6 · The paper itself

Abstract

Cardiac transcription factors are master regulators during heart development. Some were shown to transdifferentiate tail tip and cardiac fibroblasts into cardiomyocytes. However, recent studies have showed that controversies exist. Potential difference in tail tip and cardiac fibroblast isolation may possibly confound the observations. Moreover, due to the use of a cardiac reporter (Myh6) selection strategy for induced cardiomyocyte enrichment, and the lack of tracking signals for each transcription factors, individual roles of each transcription factors in activating cardiac gene expression in mammalian non-myoblastic cells have never been elucidated. Answers to these questions are an important step toward cardiomyocyte regeneration. Because mouse 10T1/2 fibroblasts are non-myoblastic in nature and can be induced to express genes of all three types of muscle cells, they are an ideal model for the analysis of cardiac and non-cardiac gene activation after induction. We constructed bi-cistronic lentiviral vectors, capable of expressing cardiac transcription factors along with different fluorescent tracking signals. By infecting 10T1/2 fibroblasts with Nkx2-5, Tbx5, Gata4 or Myocd cardiac transcription factor lentivirus alone or different combinations, we found that only Tbx5+Myocd and Tbx5+Gata4+Myocd combinations induced Myh6 and Tnnt2 cardiac marker protein expression. Microarray-based gene ontology analysis revealed that Tbx5 alone activated genes involved in the Wnt receptor signaling pathway and inhibited genes involved in a number of cardiac-related processes. Myocd alone activated genes involved in a number of cardiac-related processes and inhibited genes involved in the Wnt receptor signaling pathway and non-cardiac processes. Gata4 alone inhibited genes involved in non-cardiac processes. Tbx5+Gata4+Myocd was the most effective activator of genes associated with cardiac-related processes. Unlike Tbx5, Gata4, Myocd alone or Tbx5+Myocd, Tbx5+Gata4+Myocd activated the fewest genes associated with non-cardiac processes. Conclusively, Tbx5, Gata4 and Myocd play different roles in cardiac gene activation in mammalian non-myoblastic cells. Tbx5+Gata4+Myocd activates the most cardiac and the least non-cardiac gene expression.

Indexed as

Transcriptional ActivationAnimalsCell LineDoxycyclineFibroblastsGATA4 Transcription FactorGene Expression ProfilingGene OntologyGenetic VectorsHEK293 CellsHomeobox Protein Nkx-2.5Homeodomain ProteinsHumansLentivirusMiceMicroscopy, ConfocalDoxycyclineGata4 protein, mouseGATA4 Transcription FactorHomeobox Protein Nkx-2.5Homeodomain ProteinsMyh6 protein, mouseMyocardinMyosin Heavy ChainsNkx2-5 protein, mouseNuclear ProteinsT-Box Domain ProteinsT-box transcription factor 5Trans-ActivatorsTranscription FactorsTroponin T

Identifiers

PMID23144723
PMCPMC3483304
OpenAlexW2039092738

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.