Evidence map›Paper›PMID 25458896›Full record

ArticleStem cell reports2014

An expandable, inducible hemangioblast state regulated by fibroblast growth factor.

David T Vereide, Vernella Vickerman, Scott A Swanson, Li-Fang Chu, Brian E McIntosh, James A Thomson

Abstract read
In one paragraph

Article in Stem cell reports, 2014. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Making a Hematopoietic Stem Cell.Trends in cell biology · 2016
    Review
  12. Review
  13. Review
  14. Review
  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

6 authors.

David T VereideMorgridge Institute for Research, Madison, WI 53715, USA; Biotechnology Center, University of Wisconsin-Madison, Madison, WI 53706, USA. Electronic address: dvereide@morgridge.org.
Vernella VickermanMorgridge Institute for Research, Madison, WI 53715, USA.
Scott A SwansonMorgridge Institute for Research, Madison, WI 53715, USA.
Li-Fang ChuMorgridge Institute for Research, Madison, WI 53715, USA.
Brian E McIntoshMorgridge Institute for Research, Madison, WI 53715, USA.
James A ThomsonMorgridge Institute for Research, Madison, WI 53715, USA; Department of Cell and Regenerative Biology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA; Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA. Electronic address: jthomson@morgridge.org.

Funding

Institutional Training in the Genomic SciencesT32HG002760 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI Qiongshi Lu · 2003 to 2026
$17.7M
Midwest Progenitor Cell ConsortiumU01HL099773 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI THOMSON, JAMES ALEXANDER · 2009 to 2015
$7.8M
NHGRI NIH HHS 5T32HG002760NHGRI NIH HHS T32 HG002760NHLBI NIH HHS 1U01 HL099773-01NHLBI NIH HHS U01 HL099773
6 · The paper itself

Abstract

During development, the hematopoietic and vascular lineages are thought to descend from common mesodermal progenitors called hemangioblasts. Here we identify six transcription factors, Gata2, Lmo2, Mycn, Pitx2, Sox17, and Tal1, that "trap" murine cells in a proliferative state and endow them with a hemangioblast potential. These "expandable" hemangioblasts (eHBs) are capable, once released from the control of the ectopic factors, to give rise to functional endothelial cells, multilineage hematopoietic cells, and smooth muscle cells. The eHBs can be derived from embryonic stem cells, from fetal liver cells, or poorly from fibroblasts. The eHBs reveal a central role for fibroblast growth factor, which not only promotes their expansion, but also facilitates their ability to give rise to endothelial cells and leukocytes, but not erythrocytes. This study serves as a demonstration that ephemeral progenitor states can be harnessed in vitro, enabling the creation of tractable progenitor cell lines.

Indexed as

AnimalsBlood CellsCell DifferentiationCell LineageCell ProliferationEndothelial CellsFibroblast Growth FactorsGene Expression ProfilingHemangioblastsHigh-Throughput Nucleotide SequencingImmunophenotypingMiceMyocytes, Smooth MusclePhenotypeTranscriptomeFibroblast Growth Factors

Identifiers

PMID25458896
PMCPMC4264065

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.