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" Functional assessment of hematopoietic niche cells derived from human embryonic stem cells. "
Ferrell, Patrick IHexum, Melinda KKopher, Ross ALepley, Michael AGussiaas, AmandaKaufman, Dan Set al.
Document Type
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AL
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Record Number
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901319
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Doc. No
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LA4s74z92t
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Title & Author
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Functional assessment of hematopoietic niche cells derived from human embryonic stem cells. [Article]\ Ferrell, Patrick IHexum, Melinda KKopher, Ross ALepley, Michael AGussiaas, AmandaKaufman, Dan Set al.
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Date
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2014
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Title of Periodical
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UC San Diego
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Abstract
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To evaluate hematopoietic niche cell populations isolated from human embryonic stem cells (hESCs), we tested the ability of hESC-derived stromal lines to support CD34(+) umbilical cord blood (UCB)- and hESC-derived CD34(+)45(+) cells in long-term culture initiating cell (LTC-IC) assays. Specifically, these hematopoietic populations were cocultured with hESC-derived mesenchymal stromal cells (hESC-MSCs) and hESC-derived endothelial cells (hESC-ECs), and then assessed for their LTC-IC potential in comparison to coculture with bone marrow (BM)-derived MSCs and the mouse stromal line M2-10B4. We found that the hESC-derived stromal lines supported LTC-ICs from UCB similar to M2-10B4 cells and better than BM-MSCs. However, none of the stromal populations supported LTC-IC from hESC-derived CD34(+)45(+) cells. Engraftment data using the output from LTC-IC assays showed long-term repopulation (12 weeks) of NSG mice to correlate with LTC-IC support on a given stromal layer. Therefore, hESC-derived stromal lines can be used to efficiently evaluate putative hematopoietic stem/progenitor cells derived from hESCs or other cell sources.
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