Evidence map›Paper›PMID 21494253›Full record

ArticleLeukemia2011

Rapid mobilization of hematopoietic progenitors by AMD3100 and catecholamines is mediated by CXCR4-dependent SDF-1 release from bone marrow stromal cells.

Ayelet Dar, Amir Schajnovitz, Kfir Lapid, Alexander Kalinkovich, Tomer Itkin, Aya Ludin, Wei-Ming Kao, Michela Battista, Melania Tesio, Orit Kollet and 11 more

Erratum issuedAbstract read
In one paragraph

Article in Leukemia, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 120 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 1 pooled it
12.2field-weighted citation impact, top 1% 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

120 citing papers in PubMed, 1 synthesis or guideline pooled it, 230 citations in OpenAlex.

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  20. Closer to Nature: The Role of MSCs in Recreating the Microenvironment of the Hematopoietic Stem Cell Niche in vitro.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2022
    Review

60 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

21 authors at 6 institutions in 4 countries.

Ayelet Dar *Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Amir Schajnovitz *Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Kfir Lapid *Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Alexander KalinkovichDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Tomer ItkinDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Aya LudinDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Wei-Ming KaoDepartment of Medicine, Immunology Institute, and Black Family Stem Cell Institute, Mount Sinai School of Medicine, New York, New York, USA.
Michela BattistaDepartment of Medicine, Immunology Institute, and Black Family Stem Cell Institute, Mount Sinai School of Medicine, New York, New York, USA.
Melania TesioDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Orit KolletDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Neta Netzer CohenDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Raanan MargalitDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Eike C BussDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Francoise BaleuxInstitute Pasteur, Paris, France.
Shinya OishiGraduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan.
Nobutaka FujiiGraduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan.
Andre LarochelleMolecular Hematopoiesis Section, Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Cynthia E DunbarMolecular Hematopoiesis Section, Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Hal E BroxmeyerDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indianapolis, USA.
Paul S FrenetteDepartment of Medicine, Immunology Institute, and Black Family Stem Cell Institute, Mount Sinai School of Medicine, New York, New York, USA.
Tsvee LapidotDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Weizmann Institute of Science · ILIcahn School of Medicine at Mount Sinai · USKyoto University · JPInstitut Pasteur · FRNational Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

Understanding hematopoietic stem cell mobilization and engraftmentZIAHL006063 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DUNBAR, CYNTHIA E · 2010 to 2025
$23.5M
Role of mesenchymal stem cells in the blood stem cell nicheR01HL097819 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRENETTE, PAUL S · 2009 to 2012
$1.7M
Intramural NIH HHS ZIA HL006063NHLBI NIH HHS R01 HL097819NIMHD NIH HHS L60 MD003100
6 · The paper itself

Abstract

Steady-state egress of hematopoietic progenitor cells can be rapidly amplified by mobilizing agents such as AMD3100, the mechanism, however, is poorly understood. We report that AMD3100 increased the homeostatic release of the chemokine stromal cell derived factor-1 (SDF-1) to the circulation in mice and non-human primates. Neutralizing antibodies against CXCR4 or SDF-1 inhibited both steady state and AMD3100-induced SDF-1 release and reduced egress of murine progenitor cells over mature leukocytes. Intra-bone injection of biotinylated SDF-1 also enhanced release of this chemokine and murine progenitor cell mobilization. AMD3100 directly induced SDF-1 release from CXCR4(+) human bone marrow osteoblasts and endothelial cells and activated uPA in a CXCR4/JNK-dependent manner. Additionally, ROS inhibition reduced AMD3100-induced SDF-1 release, activation of circulating uPA and mobilization of progenitor cells. Norepinephrine treatment, mimicking acute stress, rapidly increased SDF-1 release and progenitor cell mobilization, whereas β2-adrenergic antagonist inhibited both steady state and AMD3100-induced SDF-1 release and progenitor cell mobilization in mice. In conclusion, this study reveals that SDF-1 release from bone marrow stromal cells to the circulation emerges as a pivotal mechanism essential for steady-state egress and rapid mobilization of hematopoietic progenitor cells, but not mature leukocytes.

Indexed as

AnimalsBenzylaminesBone Marrow CellsCells, CulturedChemokine CXCL12CyclamsHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHeterocyclic CompoundsHumansMiceMice, Inbred BALB CMice, Inbred C57BLNorepinephrineReceptors, CXCR4Stromal CellsBenzylaminesChemokine CXCL12CyclamsHeterocyclic CompoundsNorepinephrineplerixaforReceptors, CXCR4

Identifiers

PMID21494253
PMCPMC4175714
OpenAlexW2003829343

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.