Immortalization of bone marrow-derived human mesenchymal stem cells by removable simian virus 40T antigen gene: Analysis of the ability to support expansion of cord blood hematopoietic progenitor cells

被引:1
作者
Nishioka, K
Fujimori, Y
Hashimoto-Tamaoki, T
Kai, SR
Qiu, HY
Kobayashi, N
Tanaka, N
Westerman, KA
Leboulch, P
Hara, H
机构
[1] Hyogo Med Univ, Inst Adv Med Sci, Lab Cell Transplantat, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Med Univ, Dept Med, Div Hematol Oncol, Nishinomiya, Hyogo 6638501, Japan
[3] Hyogo Med Univ, Dept Genet, Nishinomiya, Hyogo 6638501, Japan
[4] Hyogo Med Univ, Dept Transfus Med, Nishinomiya, Hyogo 6638501, Japan
[5] Okayama Univ, Grad Sch Med & Dent, Dept Surg, Okayama 7008558, Japan
[6] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
关键词
mesenchymal stem cells; immortalization; SV40T; CD34; hematopoietic progenitor cells;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human marrow-derived mesenchymal stem cells (MSC), which have the potential to differentiate into mesenchymal tissues, such as bone, cartilage, adipose and bone marrow stroma, were transduced with a retroviral vector carrying the simian virus 40 large T antigen, hygromycin-resistant gene and herpes simplex virus thymidine kinase gene, that can be excised by Cre/loxP site-specific recombination. This resulted in establishment of an MSC cell line, HMSC-1, which retained original surface characteristics and differentiation potential, and exhibited a higher proliferative capacity than parental cells. HMSC-1 expressed mRNAs of BMP-4, Jagged-1, and SCF that are known to promote hematopoiesis. Human CB CD34(+) hematopoietic progenitor cells (HPC) cultured on a layer of HMSC-1 cells showed high expansion of CD34(+)CD38(-) immature HPC, capable of reconstituting human hematopoiesis in non-obese diabetic/severe combined immunodeficient disease (NOD/SCID) mice. This cell line may be of value for developing strategies for ex vivo expansion of human HPC.
引用
收藏
页码:925 / 932
页数:8
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