Evidence map›Paper›PMID 17416737›Full record

ArticleBlood2007

The chemokine GRObeta mobilizes early hematopoietic stem cells characterized by enhanced homing and engraftment.

Seiji Fukuda, Huimin Bian, Andrew G King, Louis M Pelus

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Review
  8. Gene Therapy and Gene Editing for β-Thalassemia.Hematology/oncology clinics of North America · 2023
    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

4 authors at 3 institutions in 1 country.

Seiji FukudaDepartment of Microbiology and Immunology, Walther Oncology Center, Indiana University School of Medicine, Indianapolis, IN, USA.
Huimin Bian
Andrew G King
Louis M Pelus
Walther Cancer Foundation · USGlaxoSmithKline (United States) · USIndiana University – Purdue University Indianapolis · US

Funding

Chemokine Induced Hematopoietic Stem Cell MobilizationR01HL069669 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI PELUS, LOUIS M · 2001 to 2009
$2.8M
Role of Survivin in Blood Stem Cell Cycle and ApoptosisR01HL079654 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI PELUS, LOUIS M · 2004 to 2007
$1.3M
NHLBI NIH HHS HL 079654NHLBI NIH HHS HL 69669NHLBI NIH HHS R01 HL069669NHLBI NIH HHS R01 HL079654
6 · The paper itself

Abstract

Mobilized peripheral blood hematopoietic stem cells (PBSCs) demonstrate accelerated engraftment compared with bone marrow; however, mechanisms responsible for enhanced engraftment remain unknown. PBSCs mobilized by GRObeta (GRObeta(Delta4)/CXCL2(Delta4)) or the combination of GRObeta(Delta4) plus granulocyte colony-stimulating factor (G-CSF) restore neutrophil and platelet recovery faster than G-CSF-mobilized PBSCs. To determine mechanisms responsible for faster hematopoietic recovery, we characterized immunophenotype and function of the GRObeta-mobilized grafts. PBSCs mobilized by GRObeta(Delta4) alone or with G-CSF contained significantly more Sca-1(+)-c-kit(+)-lineage(-) (SKL) cells and more primitive CD34(-)-SKL cells compared with cells mobilized by G-CSF and demonstrated superior competitive long-term repopulation activity, which continued to increase in secondary and tertiary recipients. GRObeta(Delta4)-mobilized SKL cells adhered better to VCAM-1(+) endothelial cells compared with G-CSF-mobilized cells. GRObeta(Delta4)-mobilized PBSCs did not migrate well to the chemokine stromal derived factor (SDF)-1alpha in vitro that was associated with higher CD26 expression. However, GRObeta(Delta4)-mobilized SKL and c-Kit(+) lineage(-) (KL) cells homed more efficiently to marrow in vivo, which was not affected by selective CXCR4 and CD26 antagonists. These data suggest that GRObeta(Delta4)-mobilized PBSCs are superior in reconstituting long-term hematopoiesis, which results from differential mobilization of early stem cells with enhanced homing and long-term repopulating capacity. In addition, homing and engraftment of GRObeta(Delta4)-mobilized cells is less dependent on the SDF-1alpha/CXCR4 axis.

Indexed as

Hematopoietic Stem Cell MobilizationPeripheral Blood Stem Cell TransplantationAnimalsAntigens, CD34Antigens, LyCell AdhesionCell MovementChemokine CXCL1Chemokine CXCL12Chemokines, CXCDipeptidyl Peptidase 4Endothelial CellsFemaleGene Expression RegulationGraft SurvivalGranulocyte Colony-Stimulating FactorAntigens, CD34Antigens, LyChemokine CXCL1Chemokine CXCL12Chemokines, CXCCxcl12 protein, mouseCxcl1 protein, mouseCXCR4 protein, mouseDipeptidyl Peptidase 4Granulocyte Colony-Stimulating FactorLy6a protein, mouseMembrane ProteinsProto-Oncogene Proteins c-kitReceptors, CXCR4Vascular Cell Adhesion Molecule-1

Identifiers

PMID17416737
PMCPMC1924764
OpenAlexW2022121473

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.