| Literature DB >> 16857897 |
Takahiro Suzuki1, Yasuhisa Yokoyama, Keiki Kumano, Minoko Takanashi, Shiro Kozuma, Tsuyoshi Takato, Tatsutoshi Nakahata, Mitsuo Nishikawa, Seiji Sakano, Mineo Kurokawa, Seishi Ogawa, Shigeru Chiba.
Abstract
Ex vivo expansion of hematopoietic stem cells (HSCs) has been explored in the fields of stem cell biology, gene therapy, and clinical transplantation. Here, we demonstrate efficient ex vivo expansion of HSCs measured by long-term severe combined immunodeficient (SCID) repopulating cells (SRCs) from human cord blood CD133-sorted cells using a soluble form of Delta1. After a 3-week culture on immobilized Delta1 supplemented with stem cell factor, thrombopoietin, Flt-3 ligand, interleukin (IL)-3, and IL-6/soluble IL-6 receptor chimeric protein (FP6) in a serum- and stromal cell-free condition, we achieved approximately sixfold expansion of SRCs when evaluated by limiting dilution/transplantation assays. The maintenance of full multipotency and self-renewal capacity during culture was confirmed by transplantation to nonobese diabetic/SCID/gammac(null) mice, which showed myeloid, B, T, and natural killer cells as well as CD133(+)CD34(+) cells, and hematopoietic reconstitution in the secondary recipients. Interestingly, the CD133-sorted cells contained approximately 4.5 times more SRCs than the CD34-sorted cells. The present study provides a promising method to expand HSCs and encourages future trials on clinical transplantation.Entities:
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Year: 2006 PMID: 16857897 DOI: 10.1634/stemcells.2006-0258
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277