Highly efficient ex vivo expansion of human hematopoietic stem cells using Delta1-Fc chimeric protein

被引:56
作者
Suzuki, Takahiro
Yokoyama, Yasuhisa
Kumano, Keiki
Takanashi, Minoko
Kozuma, Shiro
Takato, Tsuyoshi
Nakahata, Tatsutoshi
Nishikawa, Mitsuo
Sakano, Seiji
Kurokawa, Mineo
Ogawa, Seishi
Chiba, Shigeru
机构
[1] Tokyo Univ Hosp, Dept Cell Therapy & Transplantat Med, Bunkyo Ku, Tokyo 1138655, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Regenerat Med Hematopoiesis, Bunkyo Ku, Tokyo 1138655, Japan
[3] Tokyo Univ Hosp, Div Tissue Engn, Bunkyo Ku, Tokyo 1138655, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138655, Japan
[5] Japanese Red Cross Tokyo Blood Ctr, Tokyo, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Perinatal Med, Tokyo 1138655, Japan
[7] Univ Tokyo, Grad Sch Med, Dept Oral & Maxillofacial Surg, Tokyo 1138655, Japan
[8] Kyoto Univ, Grad Sch Med, Dept Pediat, Kyoto, Japan
[9] Kirin Brewery Co Ltd, Div Pharmaceut, Tokyo, Japan
[10] Asahi Kasei Corp, Corp R&D, Tokyo, Japan
[11] Asahi Kasei Corp, Cent Res Lab, Tokyo, Japan
关键词
AC133; antigen; hematopoietic stem cells; notch; stem cell expansion;
D O I
10.1634/stemcells.2006-0258
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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/gamma c(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.
引用
收藏
页码:2456 / 2465
页数:10
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