Journal of Stem Cells and Regenerative Medicine · 2017 · 13 citations · 16 references
Life SciencesCell BiologyHematologyCell DifferentiationCell ProliferationStem Cell BiologyEmbryonic Stem CellsHematopoietic DifferentiationHematopoietic Stem Cell BiologyHematopoietic Stem CellsStem Cell DifferentiationStem Cell ProliferationDifferentiation Of Hematopoietic ProgenitorsExpansionHematopoietic Stem Cell DifferentiationHematopoietic Stem Cell ExpansionHematopoietic Stem Cell ProliferationMultipotent ProgenitorsProgenitor Cells
Human embryonic stem cell (hESC)-derived hematopoietic stem/progenitor cells hold tremendous potential as alternative cell sources for the treatment of various hematological diseases, drug discovery and toxicological screening. However, limited number of hematopoietic stem/progenitor cells generated from the differentiation of hESCs hinders their downstream applications. Here, we show that aryl hydrocarbon receptor antagonist StemRegenin 1 (SR1) selectively promotes expansion of hESC-derived lin -CD34 + hematopoietic progenitors in a concentration-dependent manner. The colony-forming cell (CFC) activity was found to be enriched in the CD34 + cells that were expanded with SR1; however, these cells have less colony-forming activity as compared to unexpanded cells (1,338 vs. 7 of CD34 + cells to form 1 colony, respectively). Interestingly, SR1 showed a bipotential effect on the proliferation of CD34 negative population, that is low dose of SR1 (1 M) enhanced cell proliferation, whereas it was repressed at higher doses (>5 M). In summary, our results suggest that SR1 has the potential to facilitate expansion of hESC-derived lin -CD34 + hematopoietic progenitors, which further retain the potential to form multilineage hematopoietic colonies.
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Embryonic Stem Cell Lines Derived from Human Blastocysts
James A. Thomson, Joseph Itskovitz‐Eldor, Sander S. Shapiro et al. · Science · 1998 · 15.9K citations
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