Evidence map›Paper›PMID 9892696›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Permissive role of thrombopoietin and granulocyte colony-stimulating factor receptors in hematopoietic cell fate decisions in vivo.

R Stoffel, S Ziegler, N Ghilardi, B Ledermann, F J de Sauvage, R C Skoda

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 66 citations in OpenAlex.

  1. The role of GATA2 in adult hematopoiesis and cell fate determination.Frontiers in cell and developmental biology · 2023
    Review
  2. Towards a New Understanding of Decision-Making by Hematopoietic Stem Cells.International journal of molecular sciences · 2020
    Review
  3. Review
  4. Review
  5. Erythropoietin receptor response circuits.Current opinion in hematology · 2010
    Review
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  12. The signaling domain of the erythropoietin receptor rescues prolactin receptor-mutant mammary epithelium.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  13. Review
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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 at 2 institutions in 1 country.

R StoffelBiozentrum, University of Basel, Klingelbergstrasse 70, 4056 Basel, Switzerland.
S Ziegler
N Ghilardi
B Ledermann
F J de Sauvage
R C Skoda
University of Basel · CHNovartis (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The question of whether extracellular signals influence hematopoiesis by instructing stem cells to commit to a specific hematopoietic lineage (instructive model) or solely by permitting the survival and proliferation of predetermined progenitors (permissive model) has been controversial since the discovery of lineage-dominant hematopoietic cytokines. To study the potential role of cytokines and their receptors in hematopoietic cell fate decisions, we used homologous recombination to replace the thrombopoietin receptor gene (mpl) with a chimeric construct encoding the extracellular domain of mpl and the cytoplasmic domain of the granulocyte colony-stimulating factor receptor (G-CSFR). This chimeric receptor binds thrombopoietin but signals through the G-CSFR intracellular domain. We found that, despite the absence of a functional mpl signaling domain, homozygous knock-in mice had a normal platelet count, indicating that in vivo the cytoplasmic domain of G-CSFR can functionally replace mpl signaling to support normal megakaryopoiesis and platelet formation. This finding is compatible with the permissive model, according to which cytokine receptors provide a nonspecific survival or proliferation signal, and argues against an instructive role of mpl or G-CSFR in hematopoietic cell fate decisions.

Indexed as

Neoplasm ProteinsReceptors, CytokineAnimalsBlood PlateletsFlow CytometryHematopoiesisMegakaryocytesMiceMice, Inbred StrainsMice, KnockoutProtein BindingProto-Oncogene ProteinsReceptors, Granulocyte Colony-Stimulating FactorReceptors, ThrombopoietinRecombinant Fusion ProteinsRNA, MessengerMPL protein, humanNeoplasm ProteinsProto-Oncogene ProteinsReceptors, CytokineReceptors, Granulocyte Colony-Stimulating FactorReceptors, ThrombopoietinRecombinant Fusion ProteinsRNA, MessengerThrombopoietin

Identifiers

PMID9892696
PMCPMC15199
OpenAlexW1988846200

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.