Evidence map›Paper›PMID 20078384›Full record

ArticleCytotherapy2010

Evaluation of mobilized peripheral blood CD34(+) cells from patients with severe coronary artery disease as a source of endothelial progenitor cells.

Abba C Zubair, Sunita Malik, Athena Paulsen, Masakazu Ishikawa, Christopher McCoy, Peter X Adams, David Amrani, Marco Costa

Abstract read
In one paragraph

Article in Cytotherapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Unicentric study of cell therapy in chronic obstructive pulmonary disease/pulmonary emphysema.International journal of chronic obstructive pulmonary disease · 2011
    Trial
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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

8 authors.

Abba C ZubairTransfusion Medicine, Department of Pathology, Mayo Clinic, Jacksonville, Florida 32224, USA. zubair.abba@mayo.edu
Sunita Malik
Athena Paulsen
Masakazu Ishikawa
Christopher McCoy
Peter X Adams
David Amrani
Marco Costa

Funding

Characterization of Hematopoietic Stem CellsK23CA102824 · NCI · MAYO CLINIC JACKSONVILLE · PI ZUBAIR, ABBA C · 2003 to 2007
$656k
NCI NIH HHS CA102824NCI NIH HHS K23 CA102824
6 · The paper itself

Abstract

BACKGROUND

aimsThe distinction between hematopoietic stem cells (HSC) and endothelial progenitor cells (EPC) is poorly defined. Co-expression of CD34 antigen with vascular endothelial growth factor (VEGF) receptor (VEGFR2) is currently used to define EPC ( 1 ).

methodsWe evaluated the phenotypic and genomic characteristics of peripheral blood-derived CD34(+) cells in 22 granulocyte-colony-stimulating factor (G-CSF)-mobilized patients with severe coronary artery disease and assessed the influence of cell selection and storage on CD34(+) cell characteristics.

resultsThe median CD34(+) cell contents in the products before and after enrichment with the Isolex 300i Magnetic Cell Selection System were 0.2% and 82.5%, respectively. Cell-cycle analysis showed that 80% of CD34(+) cells were in G0 stage; 70% of the isolated CD34(+) cells co-expressed CD133, a marker for more immature progenitors. However, less than 5% of the isolated CD34(+) cells co-expressed the notch receptor Jagged-1 (CD339) and only 2% of the isolated CD34(+) population were positive for VEGFR2 (CD309). Molecular assessment of the isolated CD34(+) cells demonstrated extremely low expression of VEGFR2 and endothelial nitric oxide synthase (eNOS) and high expression of VEGF-A. Overnight storage at 4 degrees C did not significantly affect CD34(+) cell counts and viability. Storage in liquid nitrogen for 7 weeks did not affect the percentage of CD34(+) cells but was associated with a 26% drop in cell viability.

conclusionsWe have demonstrated that the majority of isolated CD34(+) cells consist of immature and quiescent cells that lack prototypic markers of EPC. High VEGF-A gene expression might be one of the mechanisms for CD34(+) cell-induced angiogenesis.

Indexed as

Hematopoietic Stem Cell MobilizationAC133 AntigenAgedAngiogenic ProteinsAntigens, CDAntigens, CD34BiomarkersCell CountCell CycleCell SeparationCell SurvivalClinical Trials, Phase II as TopicCoronary Artery DiseaseEndothelial CellsFemaleFlow CytometryAC133 AntigenAngiogenic ProteinsAntigens, CDAntigens, CD34BiomarkersGlycoproteinsPeptidesPROM1 protein, humanVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID20078384
PMCPMC3919139

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Registered trials

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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.