Source:http://linkedlifedata.com/resource/pubmed/id/11177594
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0005773,
umls-concept:C0035647,
umls-concept:C0086418,
umls-concept:C0162371,
umls-concept:C0205245,
umls-concept:C0334094,
umls-concept:C0423899,
umls-concept:C0699032,
umls-concept:C1332710,
umls-concept:C1418946,
umls-concept:C1527178,
umls-concept:C1533691,
umls-concept:C1705938,
umls-concept:C2323499
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pubmed:issue |
6
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pubmed:dateCreated |
2001-2-22
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pubmed:abstractText |
The 5-transmembrane receptor AC133 is expressed on a subpopulation of human hematopoietic cells that includes the CD34(bright) cells. We evaluated the developmental potential of AC133+CD34(bright) and AC133(dim/-)CD34+ cells isolated from 5 cord blood (CB) samples by studying the in vitro proliferative and differentiative potential of each population in both progenitor and mature cell expansion cultures. Seven-day culture of AC133+CD34(bright) cells with a cytokine combination favoring primitive progenitor cells causes a significant increase in CD34+, CFU-C and noncycling stem/progenitor cells HPP-Q (High Proliferative Potential-Quiescent), whereas culture of AC133(dim/-)CD34+ cells shows a limited increase in committed progenitor cells only. HPP-Q cells were not found in freshly isolated AC133(dim/-)CD34+ nor in expanded CD34+ cells derived from AC133(dim/-)CD34+ cells. No statistically significant difference was observed between the 1-week expanded AC133+ and the initial AC133+CD34(bright) cells regarding their clonogenic efficiency (CE), while expanded CD34+ cells derived from AC133(dim/-)CD34+ cells exhibited a decreased CE. Subexpansion of the reselected AC133+ derived from AC133+CD34(bright) cells reveals a further increase of stem/progenitor cells and the 14-day expanded AC133+ cells reveal an unchanged CE. Subexpansion of reselected 7-day CD34+ cells derived from AC133(dim/-)CD34+ cells was not possible. Culture of AC133+CD34(bright) cells in cytokines that favor megakaryopoiesis or erythropoiesis resulted in a significant expansion of CD41+ and CD71+ cells, respectively; AC133(dim/-)CD34+, in comparison, showed a limited potential to megakaryocytic differentiation and a decreased production of erythroid cells. Our data indicate that early high proliferating stem/progenitor cells and early committed progenitors are present in AC133+CD34(bright) cells, but not in AC133(dim/-)CD34+ cells; the latter represent late committed progenitors with limited proliferative potential.
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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/AC133 antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD34,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1525-8165
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
827-40
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11177594-Antigens, CD,
pubmed-meshheading:11177594-Antigens, CD34,
pubmed-meshheading:11177594-Cell Culture Techniques,
pubmed-meshheading:11177594-Cell Differentiation,
pubmed-meshheading:11177594-Cell Division,
pubmed-meshheading:11177594-Cytokines,
pubmed-meshheading:11177594-Fetal Blood,
pubmed-meshheading:11177594-Flow Cytometry,
pubmed-meshheading:11177594-Glycoproteins,
pubmed-meshheading:11177594-Hematopoietic Stem Cells,
pubmed-meshheading:11177594-Humans,
pubmed-meshheading:11177594-Immunomagnetic Separation,
pubmed-meshheading:11177594-Immunophenotyping,
pubmed-meshheading:11177594-Peptides
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pubmed:year |
2000
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pubmed:articleTitle |
A functional hierarchy among the CD34+ hematopoietic cells based on in vitro proliferative and differentiative potential of AC133+CD34(bright) and AC133(dim/)-CD34+ human cord blood cells.
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pubmed:affiliation |
Bone Marrow Transplantation Unit, St. Sophia Children's Hospital, Thivon and Levadias, Athens 11527, Greece. paedbmt@hellasnet.gr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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