Source:http://linkedlifedata.com/resource/pubmed/id/21400571
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2011-6-9
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pubmed:abstractText |
Since umbilical cord blood (UCB), contains a limited hematopoietic stem/progenitor cells (HSC) number, successful expansion protocols are needed to overcome the hurdles associated with inadequate numbers of HSC collected for transplantation. UCB cultures were performed using a human stromal-based serum-free culture system to evaluate the effect of different initial CD34(+) cell enrichments (Low: 24?±?1.8%, Medium: 46?±?2.6%, and High: 91?±?1.5%) on the culture dynamics and outcome of HSC expansion. By combining PKH tracking dye with CD34(+) and CD34(+) CD90(+) expression, we have identified early activation of CD34 expression on CD34(-) cells in Low and Medium conditions, prior to cell division (35?±?4.7% and 55?±?4.1% CD34(+) cells at day 1, respectively), affecting proliferation/cell cycle status and ultimately determining CD34(+)/CD34(+) CD90(+) cell yield (High: 14?±?1.0/3.5?±?1.4-fold; Medium: 22?±?2.0/3.4?±?1,0-fold; Low: 31?±?3.0/4.4?±?1.5-fold) after a 7-day expansion. Considering the potential benefits of using expanded UCB HSC in transplantation, here we quantified in single UCB units, the impact of using one/two immunomagnetic sorting cycles (corresponding to Medium and High initial progenitor content), and the average CD34(+) cell recovery for each strategy, on overall CD34(+) cell expansion. The higher cell recovery upon one sorting cycle lead to higher CD34(+) cell numbers after 7 days of expansion (30?±?2.0 vs. 13?±?1.0?×?10(6) cells). In particular, a high (>90%) initial progenitor content was not mandatory to successfully expand HSC, since cell populations with moderate levels of enrichment readily increased CD34 expression ex-vivo, generating higher stem/progenitor cell yields. Overall, our findings stress the importance of establishing a balance between the cell proliferative potential and cell recovery upon purification, towards the efficient and cost-effective expansion of HSC for cellular therapy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1097-4644
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
112
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1822-31
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pubmed:meshHeading |
pubmed-meshheading:21400571-Antigens, CD34,
pubmed-meshheading:21400571-Cell Culture Techniques,
pubmed-meshheading:21400571-Cell Cycle,
pubmed-meshheading:21400571-Cell Differentiation,
pubmed-meshheading:21400571-Cell Proliferation,
pubmed-meshheading:21400571-Cells, Cultured,
pubmed-meshheading:21400571-Fetal Blood,
pubmed-meshheading:21400571-Flow Cytometry,
pubmed-meshheading:21400571-Hematopoietic Stem Cells,
pubmed-meshheading:21400571-Humans,
pubmed-meshheading:21400571-Immunomagnetic Separation,
pubmed-meshheading:21400571-Leukocytes, Mononuclear,
pubmed-meshheading:21400571-Phenotype
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pubmed:year |
2011
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pubmed:articleTitle |
Initial CD34+ cell-enrichment of cord blood determines hematopoietic stem/progenitor cell yield upon ex vivo expansion.
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pubmed:affiliation |
Department of Bioengineering, Instituto Superior Técnico, Lisboa, Portugal.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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