Source:http://linkedlifedata.com/resource/pubmed/id/20728214
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2010-9-24
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pubmed:abstractText |
Extracellular adenosine removal is via human equilibrative nucleoside transporters 1 (hENT1) and 2 (hENT2) in the endothelium, thus regulating adenosine-induced revascularization and angiogenesis. Since human endothelial progenitor cells (hEPCs) promote revascularization, we hypothesize differential expression of nucleoside transporters in hEPCs. hEPCs were cultured 3 (hEPC-3d) or 14 (hEPC-14d) days. RT-PCR for prominin 1, CD34, octamer-4, kinase insert domain receptor, oxidized low-density lipoprotein (lectin-like) receptor 1 and tyrosine endothelial kinase was used to evaluate phenotypic differentiation. Flow cytometry was used to estimate CD34(+)/KDR(-) (non-differentiated), CD34(-)/KDR(+) (differentiated) or CD34(+)/KDR(+) (mixed) cell populations. Adenosine transport was measured in absence or presence of sodium, S-(4-nitrobenzyl)-6-thio-inosine (NBTI, 1-10 ?M), inosine, hypoxanthine or guanine (0.1-5 mM), hENTs protein abundance by western blot, and hENTs, hCNT1, hCNT2 and hCNT3 mRNA expression by real time RT-PCR. hEPC-3d cells were CD34(+)/KDR(-) compared with hEPC-14d cells that were CD34(-)/KDR(+). hEPC-3d cells exhibit hENT1-like adenosine transport (NBTI-sensitive, Na(+)-independent), which is absent in hEPC-14d cells. hEPC-14d cells exhibit two transport components: component 1 (NBTI insensitive, Na(+)-independent) and component 2 (NBTI insensitive, Na(+)-dependent, Hill coefficient ?1.8), the latter resembling CNT3-like transport. hEPC-3d cells express hENT1 protein and mRNA, which is reduced (?90%) in hEPC-14d cells, but instead only hCNT3 mRNA is expressed in this cell type. hENT2, hCNT1 and hCNT2 were undetectable in hEPCs. Thus, hEPCs exhibit a differential expression of hENT1 and hCNT3 functional nucleoside transporters, which could be related with its differentiation stage.
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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/4-nitrobenzylthioinosine,
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine,
http://linkedlifedata.com/resource/pubmed/chemical/Equilibrative Nucleoside...,
http://linkedlifedata.com/resource/pubmed/chemical/Equilibrative-Nucleoside...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA,
http://linkedlifedata.com/resource/pubmed/chemical/Thioinosine
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1532-3102
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
928-36
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pubmed:meshHeading |
pubmed-meshheading:20728214-Adenosine,
pubmed-meshheading:20728214-Biological Transport,
pubmed-meshheading:20728214-Blotting, Western,
pubmed-meshheading:20728214-Cell Differentiation,
pubmed-meshheading:20728214-Endothelial Cells,
pubmed-meshheading:20728214-Equilibrative Nucleoside Transporter 1,
pubmed-meshheading:20728214-Equilibrative-Nucleoside Transporter 2,
pubmed-meshheading:20728214-Humans,
pubmed-meshheading:20728214-Kinetics,
pubmed-meshheading:20728214-RNA,
pubmed-meshheading:20728214-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20728214-Stem Cells,
pubmed-meshheading:20728214-Thioinosine
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pubmed:year |
2010
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pubmed:articleTitle |
Differential expression of functional nucleoside transporters in non-differentiated and differentiated human endothelial progenitor cells.
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pubmed:affiliation |
Department of Clinical Biochemistry and Immunology, Faculty of Pharmacy, Universidad de Concepción, Chile.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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