Evidence map›Paper›PMID 26105053›Full record

ArticleThe Journal of biological chemistry2015

Dickkopf Homolog 3 Induces Stem Cell Differentiation into Smooth Muscle Lineage via ATF6 Signalling.

Xiaocong Wang, Eirini Karamariti, Russell Simpson, Wen Wang, Qingbo Xu

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  11. tRNA-derived fragments tRFMolecular therapy. Nucleic acids · 2021
    Article
  12. Protein quality control of cell stemness.Cell regeneration (London, England) · 2020
    Review
  13. Review
  14. Article
  15. Observational
  16. Article
  17. Article
  18. Review
  19. Dickkopf-3 in aberrant endothelial secretome triggers renal fibroblast activation and endothelial-mesenchymal transition.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2019
    Article
  20. 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 2 institutions in 1 country.

Xiaocong WangFrom the Cardiovascular Division, King's College London BHF Centre, London SE5 9NU, United Kingdom and the Institute of Bioengineering, Queen Mary University of London, London E1 4NS, United Kingdom.
Eirini KaramaritiFrom the Cardiovascular Division, King's College London BHF Centre, London SE5 9NU, United Kingdom and.
Russell SimpsonFrom the Cardiovascular Division, King's College London BHF Centre, London SE5 9NU, United Kingdom and.
Wen Wangthe Institute of Bioengineering, Queen Mary University of London, London E1 4NS, United Kingdom wen.wang@qmul.ac.uk.
Qingbo XuFrom the Cardiovascular Division, King's College London BHF Centre, London SE5 9NU, United Kingdom and qingbo.xu@kcl.ac.uk.
King's College London · GBQueen Mary University of London · GB

Funding

British Heart Foundation RG/09/004/27647British Heart Foundation RG/14/6/31144
6 · The paper itself

Abstract

Smooth muscle cells (SMCs) are a key component of healthy and tissue engineered vessels and play a crucial role in vascular development and the pathogenic events of vascular remodeling i.e. restenosis. However, the cell source from which they can be isolated is limited. Embryonic stem (ES) cells that have the remarkable capability to differentiate into vascular SMCs in response to specific stimuli provide a useful model for studying SMC differentiation. Previous studies suggested that dickkopf homolog 3 (DKK3) has a role in human partially induced pluripotent stem cell to SMC differentiation. Here, we demonstrate that the expression of DKK3 is essential for the expression of SMC markers and myocardin at both the mRNA and protein levels during mouse ES cell differentiation into SMCs (ESC-SMC differentiation). Overexpression of DKK3 leads to further up-regulation of the aforementioned markers. Further investigation indicates that DKK3 added as a cytokine activates activating transcription factor 6 (ATF6), leading to the increased binding of ATF6 on the myocardin promoter and increased its expression. In addition, inhibition of extracellular signal-regulated kinases 1/2 (ERK1/2) promotes the expression of ATF6 and leads to further increase of myocardin transcription. Our findings offer a novel mechanism by which DKK3 regulates ESC-SMC differentiation by activating ATF6 and promoting myocardin expression.

Indexed as

Activating Transcription Factor 6Adaptor Proteins, Signal TransducingAnimalsBinding SitesCell DifferentiationCell LineCell LineageEmbryo, MammalianEmbryonic Stem CellsFlavonoidsGene Expression Regulation, DevelopmentalIntercellular Signaling Peptides and ProteinsMiceMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myocardin2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-oneActivating Transcription Factor 6Adaptor Proteins, Signal TransducingAtf6 protein, mouseDkk3 protein, mouseFlavonoidsIntercellular Signaling Peptides and ProteinsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MyocardinNuclear ProteinsProtein Kinase InhibitorsRNA, MessengerTrans-Activatorscardiovascular diseasecytokinedifferentiationmyocardinsmooth musclestem cells

Identifiers

PMID26105053
PMCPMC4528144
OpenAlexW1962157876

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.