Evidence map›Paper›PMID 28323620›Full record

ArticleeLife2017

Discovery of novel determinants of endothelial lineage using chimeric heterokaryons.

Wing Tak Wong, Gianfranco Matrone, XiaoYu Tian, Simion Alin Tomoiaga, Kin Fai Au, Shu Meng, Sayumi Yamazoe, Daniel Sieveking, Kaifu Chen, David M Burns and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Cell Fusion in Reprogramming and Regeneration.Advances in experimental medicine and biology · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. A Missing LNC in Vascular Diseases.Circulation research · 2017
    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

13 authors at 3 institutions in 1 country.

Wing Tak WongDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.
Gianfranco MatroneDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.ORCID 0000-0002-6064-0734
XiaoYu TianDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.
Simion Alin TomoiagaDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.
Kin Fai AuDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.
Shu MengDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.
Sayumi YamazoeDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States.
Daniel SievekingDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States.
Kaifu ChenDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.
David M BurnsBaxter Laboratory for Stem Cell Biology, Stanford University School of Medicine, Stanford, United States.
James K ChenDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States.
Helen M BlauBaxter Laboratory for Stem Cell Biology, Stanford University School of Medicine, Stanford, United States.
John P CookeDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States.ORCID 0000-0003-0033-9138
Houston Methodist · USStanford University · USUniversity of Iowa · US

Funding

TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI COVERT, MARKUS W · 2013 to 2017
$10.9M
Basic and Translational Research iPSC-based hematologic and vascular therapiesU01HL100397 · NHLBI · STANFORD UNIVERSITY · PI COOKE, JOHN P · 2009 to 2015
$7.4M
NCE-based strategy for nuclear reprogramming and regenerative medicineRC2HL103400 · NHLBI · STANFORD UNIVERSITY · PI COOKE, JOHN P · 2009 to 2010
$2.7M
Bioinformatics platform for Hybrid-Seq transcriptome data analysisR01HG008759 · NHGRI · UNIVERSITY OF IOWA · PI AU, KIN FAI · 2016 to 2020
$1.9M
NHGRI NIH HHS R01 HG008759NHLBI NIH HHS RC2 HL103400NHLBI NIH HHS U01 HL100397NIGMS NIH HHS P50 GM107615
6 · The paper itself

Abstract

We wish to identify determinants of endothelial lineage. Murine embryonic stem cells (mESC) were fused with human endothelial cells in stable, non-dividing, heterokaryons. Using RNA-seq, it is possible to discriminate between human and mouse transcripts in these chimeric heterokaryons. We observed a temporal pattern of gene expression in the ESCs of the heterokaryons that recapitulated ontogeny, with early mesodermal factors being expressed before mature endothelial genes. A set of transcriptional factors not known to be involved in endothelial development was upregulated, one of which was POU class 3 homeobox 2 (Pou3f2). We confirmed its importance in differentiation to endothelial lineage via loss- and gain-of-function (LOF and GOF). Its role in vascular development was validated in zebrafish embryos using morpholino oligonucleotides. These studies provide a systematic and mechanistic approach for identifying key regulators in directed differentiation of pluripotent stem cells to somatic cell lineages.

Indexed as

AnimalsCell DifferentiationCell FusionEmbryonic Stem CellsEndothelial CellsGene Expression ProfilingHumansMiceZebrafishcell biologydevelopmental biologyEndothelial lineageHeterokaryonshumanmousenuclear reprogrammingpou3f2stem cellszebrafish

Identifiers

PMID28323620
PMCPMC5391207
OpenAlexW2599909009

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.