Evidence map›Paper›PMID 19197139›Full record

ArticleThe Journal of clinical investigation2009

MT1-MMP and RECK are involved in human CD34+ progenitor cell retention, egress, and mobilization.

Yaron Vagima, Abraham Avigdor, Polina Goichberg, Shoham Shivtiel, Melania Tesio, Alexander Kalinkovich, Karin Golan, Ayelet Dar, Orit Kollet, Isabelle Petit and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

55 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
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  7. The Role of Circulating Biomarkers in Peripheral Arterial Disease.International journal of molecular sciences · 2021
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  8. Article
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  15. Extracellular molecules in hematopoietic stem cell mobilisation.International journal of hematology · 2017
    Review
  16. Review
  17. Article
  18. Review
  19. Hematopoietic Stem Cell and Its Bone Marrow Niche.Current topics in developmental biology · 2016
    Review
  20. 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

18 authors at 3 institutions in 1 country.

Yaron VagimaImmunology Department,Weizmann Institute of Science, Hertzl Str., Rehovot, Israel.
Abraham Avigdor
Polina Goichberg
Shoham Shivtiel
Melania Tesio
Alexander Kalinkovich
Karin Golan
Ayelet Dar
Orit Kollet
Isabelle Petit
Orly Perl
Ester Rosenthal
Igor Resnick
Izhar Hardan
Yechiel N Gellman
David Naor
Arnon Nagler
Tsvee Lapidot
Weizmann Institute of Science · ILSheba Medical Center · ILHebrew University of Jerusalem · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanisms governing hematopoietic progenitor cell mobilization are not fully understood. We report higher membrane type 1-MMP (MT1-MMP) and lower expression of the MT1-MMP inhibitor, reversion-inducing cysteine-rich protein with Kazal motifs (RECK), on isolated circulating human CD34+ progenitor cells compared with immature BM cells. The expression of MT1-MMP correlated with clinical mobilization of CD34+ cells in healthy donors and patients with lymphoid malignancies. Treatment with G-CSF further increased MT1-MMP and decreased RECK expression in human and murine hematopoietic cells in a PI3K/Akt-dependent manner, resulting in elevated MT1-MMP activity. Blocking MT1-MMP function by Abs or siRNAs impaired chemotaxis and homing of G-CSF-mobilized human CD34+ progenitors. The mobilization of immature and maturing human progenitors in chimeric NOD/SCID mice by G-CSF was inhibited by anti-MT1-MMP treatment, while RECK neutralization promoted motility and egress of BM CD34+ cells. BM c-kit+ cells from MT1-MMP-deficient mice also exhibited inferior chemotaxis, reduced homing and engraftment capacities, and impaired G-CSF-induced mobilization in murine chimeras. Membranal CD44 cleavage by MT1-MMP was enhanced following G-CSF treatment, reducing CD34+ cell adhesion. Accordingly, CD44-deficient mice had a higher frequency of circulating progenitors. Our results reveal that the motility, adhesion, homing, and mobilization of human hematopoietic progenitor cells are regulated in a cell-autonomous manner by dynamic and opposite changes in MT1-MMP and RECK expression.

Indexed as

AnimalsAntigens, CDAntigens, CD34Bone Marrow CellsCell MovementChemotaxisChimeraGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticGPI-Linked ProteinsGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHumansMatrix Metalloproteinase 14Membrane GlycoproteinsAntigens, CDAntigens, CD34GPI-Linked ProteinsGranulocyte Colony-Stimulating FactorMatrix Metalloproteinase 14Membrane GlycoproteinsRECK protein, humanRNA, MessengerRNA, Small Interfering

Identifiers

PMID19197139
PMCPMC2648678
OpenAlexW2102306220

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.