Evidence map›Paper›PMID 20826720›Full record

ArticleBlood2010

Evidence that growth factor independence 1b regulates dormancy and peripheral blood mobilization of hematopoietic stem cells.

Cyrus Khandanpour, Ehssan Sharif-Askari, Lothar Vassen, Marie-Claude Gaudreau, Jinfang Zhu, William E Paul, Taro Okayama, Christian Kosan, Tarik Möröy

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 76 citations in OpenAlex.

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  19. Mouse Models of Erythropoiesis and Associated Diseases.Methods in molecular biology (Clifton, N.J.) · 2018
    Review
  20. Haematologica · 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

9 authors at 5 institutions in 3 countries.

Cyrus KhandanpourInstitut de recherches cliniques de Montréal, Canada.
Ehssan Sharif-Askari
Lothar Vassen
Marie-Claude Gaudreau
Jinfang Zhu
William E Paul
Taro Okayama
Christian Kosan
Tarik Möröy
Montreal Clinical Research Institute · CANational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversité de Montréal · CAUniversity of Duisburg-Essen · DE

Funding

Interleukin 4ZIAAI000493 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2017
$11.5M
Canadian Institutes of Health Research MOP-84 238Canadian Institutes of Health Research MOP-94 846
6 · The paper itself

Abstract

Donor-matched transplantation of hematopoietic stem cells (HSCs) is widely used to treat hematologic malignancies but is associated with high mortality. The expansion of HSC numbers and their mobilization into the bloodstream could significantly improve therapy. We report here that adult mice conditionally deficient for the transcription Growth factor independence 1b (Gfi1b) show a significant expansion of functional HSCs in the bone marrow and blood. Despite this expansion, Gfi1b(ko/ko) HSCs retain their ability to self-renew and to initiate multilineage differentiation but are no longer quiescent and contain elevated levels of reactive oxygen species. Treatment of Gfi1b(ko/ko) mice with N-acetyl-cystein significantly reduced HSC numbers indicating that increased reactive oxygen species levels are at least partially responsible for the expansion of Gfi1b-deficient HSCs. Moreover, Gfi1b(-/-) HSCs show decreased expression of CXCR4 and Vascular cell adhesion protein-1, which are required to retain dormant HSCs in the endosteal niche, suggesting that Gfi1b regulates HSC dormancy and pool size without affecting their function. Finally, the additional deletion of the related Gfi1 gene in Gfi1b(ko/ko) HSCs is incompatible with the maintenance of HSCs, suggesting that Gfi1b and Gfi1 have partially overlapping functions but that at least one Gfi gene is essential for the generation of HSCs.

Indexed as

Cell MovementAcetylcysteineAmine Oxidase (Copper-Containing)AnimalsCell Adhesion MoleculesDNA-Binding ProteinsHematopoietic Stem CellsHomeostasisMiceMice, KnockoutProto-Oncogene ProteinsReactive Oxygen SpeciesReceptors, CXCR4Repressor ProteinsTranscription FactorsAcetylcysteineAmine Oxidase (Copper-Containing)Cell Adhesion MoleculesCXCR4 protein, mouseDNA-Binding ProteinsGfi1b protein, mouseGfi1 protein, mouseProto-Oncogene ProteinsReactive Oxygen SpeciesReceptors, CXCR4Repressor Proteinssemicarbazide-sensitive amine oxidase-vascular adhesion protein-1, mouseTranscription Factors

Identifiers

PMID20826720
PMCPMC3321835
OpenAlexW1968501325

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.