Evidence map›Paper›PMID 16407844›Full record

ArticleOncogene2006

Erythroid progenitor renewal versus differentiation: genetic evidence for cell autonomous, essential functions of EpoR, Stat5 and the GR.

H Dolznig, F Grebien, E M Deiner, K Stangl, A Kolbus, B Habermann, M A Kerenyi, M Kieslinger, R Moriggl, H Beug and 1 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

33 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  3. AcuteFrontiers in microbiology · 2020
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  19. Ineffective erythropoiesis with reduced red blood cell survival in serotonin-deficient mice.Proceedings of the National Academy of Sciences of the United States of America · 2011
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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

11 authors at 4 institutions in 1 country.

H DolznigInstitute of Molecular Pathology, Vienna Biocenter (VBC), Austria.
F Grebien
E M Deiner
K Stangl
A Kolbus
B Habermann
M A Kerenyi
M Kieslinger
R Moriggl
H Beug
E W Müllner
Vienna Biocenter · ATMax Perutz Labs · ATMedical University of Vienna · ATResearch Institute of Molecular Pathology · AT

Funding

Austrian Science Fund FWF F 2801Austrian Science Fund FWF F 2802Austrian Science Fund FWF F 2807Austrian Science Fund FWF F 2809
6 · The paper itself

Abstract

The balance between hematopoietic progenitor commitment and self-renewal versus differentiation is controlled by various transcriptional regulators cooperating with cytokine receptors. Disruption of this balance is increasingly recognized as important in the development of leukemia, by causing enhanced renewal and differentiation arrest. We studied regulation of renewal versus differentiation in primary murine erythroid progenitors that require cooperation of erythropoietin receptor (EpoR), the receptor tyrosine kinase c-Kit and a transcriptional regulator (glucocorticoid receptor; GR) for sustained renewal. However, mice defective for GR- (GR(dim/dim)), EpoR- (EpoR(H)) or STAT5ab function (Stat5ab(-/-)) show no severe erythropoiesis defects in vivo. Using primary erythroblast cultures from these mutants, we present genetic evidence that functional GR, EpoR, and Stat5 are essential for erythroblast renewal in vitro. Cells from GR(dim/dim), EpoR(H), and Stat5ab(-/-) mice showed enhanced differentiation instead of renewal, causing accumulation of mature cells and gradual proliferation arrest. Stat5ab was additionally required for Epo-induced terminal differentiation: differentiating Stat5ab(-/-) erythroblasts underwent apoptosis instead of erythrocyte maturation, due to absent induction of the antiapoptotic protein Bcl-X(L). This defect could be fully rescued by exogenous Bcl-X(L). These data suggest that signaling molecules driving leukemic proliferation may also be essential for prolonged self-renewal of normal erythroid progenitors.

Indexed as

Cell DifferentiationCell ProliferationAnimalsApoptosisbcl-X ProteinBlotting, WesternCells, CulturedEmbryo, MammalianErythroblastsErythroid Precursor CellsFlow CytometryHumansLiverMiceReceptors, ErythropoietinReceptors, Glucocorticoidbcl-X ProteinReceptors, ErythropoietinReceptors, GlucocorticoidSTAT5 Transcription Factor

Identifiers

PMID16407844
PMCPMC3035873
OpenAlexW2095784946

What OpenQuestion holds

Textmetadata
LicenceTDM
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.