Home LiteratureArticle Details
PMID: 10340407 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Rapid ex vivo expansion of human umbilical cord hematopoietic progenitors using a novel culture system.

Experimental hematology ·Vol. 27 ·No. 5 ·1999-05-00 ·Pages 904-15

Kawada H, Ando K, Tsuji T, Shimakura Y, Nakamura Y, Chargui J, Hagihara M, Itagaki H, Shimizu T, Inokuchi S, Kato S, Hotta T

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.

MeSH Terms
Animals Cell Culture Techniques/methods Cell Division/drug effects Culture Media, Serum-Free Hematopoietic Stem Cells/cytology,immunology,ultrastructure Humans Immunophenotyping Mice Microscopy, Electron, Scanning Proto-Oncogene Proteins/pharmacology Receptor Protein-Tyrosine Kinases/pharmacology Stromal Cells/cytology Thrombopoietin/pharmacology Tumor Cells, Cultured Umbilical Cord/cytology fms-Like Tyrosine Kinase 3
Chemicals
Culture Media, Serum-Free Proto-Oncogene Proteins Thrombopoietin FLT3 protein, human Flt3 protein, mouse Receptor Protein-Tyrosine Kinases fms-Like Tyrosine Kinase 3
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Kawada H
Research Center for Genetic Engineering and Cell Transplantation, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
Ando K
Tsuji T
Shimakura Y
Nakamura Y
Chargui J
Hagihara M
Itagaki H
Shimizu T
Inokuchi S
Kato S
Hotta T
Article Info
Journal
Experimental hematology
Abbr.
Exp Hematol
ISSN
0301-472X
Published
1999-05-00
Pages
904-15
Language
English
Region
Netherlands
NLM ID
0402313
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com