Source:http://linkedlifedata.com/resource/pubmed/id/10759722
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2000-6-2
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pubmed:abstractText |
The objective of this study was to evaluate the cycling status of cord blood (CB)-derived colony-forming cells (CFC) and long-term culture-initiating cells (LTC-IC), and their recruitment into the S-phase of the cell cycle. By using the cytosine arabinoside (Ara-C) suicide approach, we found that only small proportions of both CFC and LTC-IC were in the S-phase of the cell cycle. These estimates were confirmed by flow cytometric DNA analysis, which showed that 96 +/- 2% of CB-derived CD34+ cells were in G0/G1 and only 1.6 +/- 0.4% in the S-phase. Staining of CD34+ cells with an antistatin monoclonal antibody, a marker of the G0 phase, indicated that among CD34+ cells with a flow cytometric DNA content typical of the G0/G1 phase 68 +/- 7% of cells were in the G0 phase of the cell cycle. Incubation (24 h) with interleukin 3 (IL-3), recombinant human stem cell factor (SCF) and granulocyte colony-stimulating factor (G-CSF) significantly increased the proportion of cells in the S-phase for both CFC and LTC-IC without inducing any loss in numbers. Flow cytometric DNA analysis also showed an increase in CD34+ cells in the S-phase upon continuous exposure to these cytokines. Our findings indicate that: (i) very few CB-derived CFC or LTC-IC were in the S-phase of the cell cycle; (ii) a substantial amount of CD34+ cells with a flow cytometric DNA content typical of the G0/G1 fraction was cycling, as found in the G1 phase of the cell cycle; and (iii) 24-h incubation with IL-3, SCF and G-CSF could drive a proportion of progenitor cells into the S-phase without reducing their number. These data might be useful for gene transfer protocols and the ex vivo expansion of CB-derived progenitor cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD34,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/EEF1A2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Granulocyte Colony-Stimulating...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-3,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Elongation Factor 1,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Stem Cell Factor
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0007-1048
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pubmed:author |
pubmed-author:BergamaschiGG,
pubmed-author:CazzolaMM,
pubmed-author:DanovaMM,
pubmed-author:De AmiciMM,
pubmed-author:InvernizziRR,
pubmed-author:LucotteGG,
pubmed-author:MalabarbaLL,
pubmed-author:PecciAA,
pubmed-author:PerottiCC,
pubmed-author:RamajoliII,
pubmed-author:RostiVV,
pubmed-author:SalvaneschiLL,
pubmed-author:TorrettiDD
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pubmed:issnType |
Print
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pubmed:volume |
108
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
621-8
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:10759722-Antigens, CD34,
pubmed-meshheading:10759722-Cell Cycle,
pubmed-meshheading:10759722-Cell Cycle Proteins,
pubmed-meshheading:10759722-Cells, Cultured,
pubmed-meshheading:10759722-Fetal Blood,
pubmed-meshheading:10759722-Flow Cytometry,
pubmed-meshheading:10759722-Granulocyte Colony-Stimulating Factor,
pubmed-meshheading:10759722-Hematopoietic Stem Cells,
pubmed-meshheading:10759722-Humans,
pubmed-meshheading:10759722-Interleukin-3,
pubmed-meshheading:10759722-Peptide Elongation Factor 1,
pubmed-meshheading:10759722-Proteins,
pubmed-meshheading:10759722-Recombinant Proteins,
pubmed-meshheading:10759722-S Phase,
pubmed-meshheading:10759722-Stem Cell Factor
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pubmed:year |
2000
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pubmed:articleTitle |
Cell cycle distribution of cord blood-derived haematopoietic progenitor cells and their recruitment into the S-phase of the cell cycle.
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pubmed:affiliation |
Department of Internal Medicine and Medical Therapy, University of Pavia School of Medicine, Pavia, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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