Source:http://linkedlifedata.com/resource/pubmed/id/16584600
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2006-4-4
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pubmed:abstractText |
The objective of this study was to explore the supportive effects of human aorta-gonad-mesonephros (AGM)-derived stromal cells on human umbilical cord blood long-term culture-initiating cells (LTC-IC). A co-culture system was established with human AGM stromal cells and umbilical cord blood CD34(+) cells. Different stromal cells derived from human AGM region (hAGM S1-S5) were plated on 24-well plates as feeder cells. CD34(+) cells were positively selected from human umbilical cord blood through immunomagnetic bead selection method, seeded on the feeder cells, and co-cultured for 8 weeks. The hematopoietic cells were collected at 5, 6, 7 and 8 weeks for CFC analysis. Frequencies of LTC-IC in umbilical cord blood CD34(+) cells after co-culture with AGM stromal cells were detected through limiting dilute analysis (LDA). The results showed that there was no any hematopoietic CFC in the feeder cell-free culture system after 5 weeks of co-culture. However, in AGM feeder cells culture systems, there were still CFCs after 5 weeks of co-culture, which indicated that human AGM stromal cells could maintain LTC-IC in vitro. In groups of hAGM feeders, hAGMS3 and S4 had better supportive effects than other AGM groups (P < 0.05). The absolute number of LTC-IC in hAGM S3 and S4 culture systems got expansion up to (176 +/- 46)% and (187 +/- 52)% respectively without significant difference between hAGMS3 and S4 (P > 0.05). It is concluded that human AGM stromal cells S1-S5 support the maintenance of umbilical blood LTC-IC in vitro, while hAGMS3 and S4 cells have better effects on maintaining LTC-IC and expansion of LTC-IC.
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pubmed:language |
chi
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1009-2137
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
94-7
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:16584600-Aorta,
pubmed-meshheading:16584600-Cell Culture Techniques,
pubmed-meshheading:16584600-Cells, Cultured,
pubmed-meshheading:16584600-Coculture Techniques,
pubmed-meshheading:16584600-Colony-Forming Units Assay,
pubmed-meshheading:16584600-Embryo, Mammalian,
pubmed-meshheading:16584600-Fetal Blood,
pubmed-meshheading:16584600-Gonads,
pubmed-meshheading:16584600-Hematopoietic Stem Cell Mobilization,
pubmed-meshheading:16584600-Hematopoietic Stem Cells,
pubmed-meshheading:16584600-Humans,
pubmed-meshheading:16584600-Mesonephros,
pubmed-meshheading:16584600-Stromal Cells
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pubmed:year |
2006
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pubmed:articleTitle |
[Supportive effects of human aorta-gonad-mesonephros-derived stromal cells on umbilical cord blood LTC-IC].
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pubmed:affiliation |
Center for Stem Cell Research, The Second Affiliated Hospital, Sun Yat-sen University, Guangzhou 510120, China.
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pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
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