Title of article
Rapid ex vivo expansion of human umbilical cord hematopoietic progenitors using a novel culture system
Author/Authors
Hiroshi Kawada، نويسنده , , Kiyoshi Ando، نويسنده , , Takashi Tsuji، نويسنده , , Yasuhito Shimakura، نويسنده , , Yoshihiko Nakamura، نويسنده , , Jamel Chargui، نويسنده , , Masao Hagihara، نويسنده , , Hiroyuki Itagaki، نويسنده , , Takashi Shimizu، نويسنده , , Sadaki Inokuchi، نويسنده , , Shunichi Kato، نويسنده , , Tomomitsu Hotta، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1999
Pages
12
From page
904
To page
915
Abstract
Cell numbers limit the widespread clinical use of cord blood (CB) for gene therapy and marrow replacement in adults; a simple and effective method for ex vivo expansion of CB primitive progenitor cells (PPC) is required. Recently, the combination of thrombopoietin (TPO) and Flk-2/Flt-3 ligand (FL-2) was reported to support slow proliferation of CB-PPC in stroma-free liquid culture. We established a novel culture system in which the murine stromal cell line HESS-5 dramatically supports the rapid expansion of cryopreserved CB-PPC in synergy with TPO/FL-2. Furthermore, while HESS-5 cells directly adhered to human progenitors during culture, the cultured human cells could easily be harvested without contamination by HESS-5 cells. Within 7 days of culture, a 100-fold increase in CD34bright/CD38dim cells was obtained in serum-containing culture. When HESS-5 cells were physically separated from human progenitor cells in the presence of TPO/FL-2, synergy was blocked, suggesting that HESS-5 cells support proliferation of PPC by direct cell-to-cell interaction. The hematopoietic-supportive effects of this xenogeneic coculture system were then assessed in a very short-term (5 days) serum-free culture. Expansion was further enhanced by addition of stem cell factor (SCF) or interleukin-3 (IL-3). As a result, a 50- to 100-fold increase in CD34bright/CD38dim cells was noted. Colony-forming units in culture (CFU-C) and mixed colonies (CFU-GEMM) were enhanced by 10- to 30-fold and 10- to 20-fold, respectively. Moreover, generation of long-term-culture–initiating cells (LTC-IC) from CD34bright/CD38dim cells was amplified by 25-fold. The severe-combined immunodeficient (SCID) mouse-repopulating cell (SRC) assay confirmed extensive ability of the expanded cells to reconstitute long-term hematopoiesis. These results indicate that this xenogeneic coculture system, in combination with human cytokines, can rapidly generate PPC from cryopreserved CB.
Keywords
Ex vivo expansion—Progenitor cells—Stromal cell line—Thrombopoietin—Flk-2/Flt-3 ligand
Journal title
Experimental Hematology
Serial Year
1999
Journal title
Experimental Hematology
Record number
513047
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