Evidence map›Paper›PMID 24100450›Full record

ArticleBlood2013

BMP-mediated specification of the erythroid lineage suppresses endothelial development in blood island precursors.

Candace T Myers, Paul A Krieg

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. 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
3.0field-weighted citation impact, top 9% 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, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. A Molecular atlas of Xenopus respiratory system development.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Article
  14. Redox regulation of endothelial cell fate.Cellular and molecular life sciences : CMLS · 2014
    Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Candace T MyersDepartment of Molecular and Cellular Biology, and.
Paul A Krieg
University of Arizona · US

Funding

GRADUATE TRAINING IN BIOCHEMISTRY AND MOLECULAR BIOLOGYT32GM008659 · NIGMS · UNIVERSITY OF ARIZONA · PI CAPALDI, ANDREW PAUL, WEINERT, TED A. · 1997 to 2019
$5.3M
Regulation of Vascular Endothelial Gene ExpressionR01HL093694 · NHLBI · UNIVERSITY OF ARIZONA · PI KRIEG, PAUL ANTHONY · 2009 to 2010
$744k
NHLBI NIH HHS HL093694NHLBI NIH HHS R01 HL093694NIGMS NIH HHS T32 GM008659NIGMS NIH HHS T32 GM08659
6 · The paper itself

Abstract

The developmental relationship between the blood and endothelial cell (EC) lineages remains unclear. In the extra-embryonic blood islands of birds and mammals, ECs and blood cells are closely intermixed, and blood island precursor cells in the primitive streak express many of the same molecular markers, leading to the suggestion that both lineages arise from a common precursor, called the hemangioblast. Cells within the blood island of Xenopus also coexpress predifferentiation markers of the blood and EC lineages. However, using multiple assays, we find that precursor cells in the Xenopus blood island do not normally differentiate into ECs, suggesting that classic hemangioblasts are rare or nonexistent in Xenopus. What prevents these precursor cells from developing into mature ECs? We have found that bone morphogenetic protein (BMP) signaling is essential for erythroid differentiation, and in the absence of BMP signaling, precursor cells adopt an EC fate. Furthermore, inhibition of the erythroid transcription pathway leads to endothelial differentiation. Our results indicate that bipotential endothelial/erythroid precursor cells do indeed exist in the Xenopus blood island, but BMP signaling normally acts to constrain EC fate. More generally, these results provide evidence that commitment to the erythroid lineage limits development of bipotential precursors toward an endothelial fate.

Indexed as

AnimalsAnimals, Genetically ModifiedBone Morphogenetic ProteinsCell DifferentiationCell LineageCell MovementEmbryo, NonmammalianEndothelial CellsEndotheliumErythroid Precursor CellsErythropoiesisGene Expression Regulation, DevelopmentalGene Knockdown TechniquesHemangioblastsHematopoietic SystemIn Situ HybridizationBone Morphogenetic ProteinsLDN 193189PyrazolesPyrimidinesXenopus Proteins

Identifiers

PMID24100450
PMCPMC3854112
OpenAlexW1970051600

What OpenQuestion holds

Textmetadata
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.